Novartis AG

Job ID 352178BR Mar 23, 2023 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. In this role you will be accountable for contributing to developing overall, cross-functional programs of a priority disease area/ asset, especially early in lifecycle – focused on shaping assets with strong commercial potential in line with TA priorities. The role provides direction and functional expertise in a cross-functional disease area/ asset team and prioritizes US first with enhanced focus on major markets (e.g., China, Japan, Germany) and ensure close collaboration with Strategy and Early Product, NIBR, GDD and MAP teams. Major responsibilities: • DA / Asset strategy aligned with Therapeutic Area (TA) strategy: Collaborating to ensure definition and execution of a competitive strategy to establish Novartis as true industry leader within the DA/ asset and maximize patient impact by influencing/ partnering across the disease ecosystem. • Asset shaping : Shaping market-relevant assets to become Standard of Care with a focus on US • Collaborate to develop transformative, US-centric Target Product Profiles (TPPs) that are tangible, provide a clear guidance to the GDD organization on what level of evidence is required. • Make data-driven, decisive tradeoffs between needs of US and major markets (e.g., CN, JP, DE) • Integrated early brand strategies: Collaborate to ensure impactful, actionable early brand strategies until handover to International by co-developing Integrated Insights Plan, consolidating and aligning inputs and requirements across functions to achieve deep DA ecosystem understanding (patient journey, competitive, access landscape, HCS budget impact and cost effectiveness analysis) • Brand management across the lifecycle: Accountable for maintaining the integrity, consistency, and evolution of each brand across the lifecycle • Work in a diverse, high performance, cross-functionally matrixed team including identifying and integrating expertise and inputs required from other teams to ensure successful delivery (e.g., MAP) Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you'll bring to the role: • At least 10 years senior level pharmaceutical commercial, marketing, medical, access or R&D experience successfully driving growth of multiple brands • Deep disease area and asset knowledge (or track record to acquire required DA / asset expertise effectively and rapidly) Preferred: • Experience of strategy development and asset shaping early in lifecycle (from any functional perspective – marketing, new products, access, medical, clinical, R&D) • Prior experience in launching specialty brand(s) in major market(s) (US, CN, JP, EU5, AUS, CAN) • Significant (3+ years) and recent (post 2015) experience in above country (regional or global) role • Significant (3+ years) and recent (post 2015) local US experience preferred; Local US experience includes working in the US market with the local US customers, US health care systems/ systems of care, US payors/ accounts, etc.), driving US market strategy • Established relationships with relevant Global KOLs • Proven experience credibly interacting and influencing stakeholders in research and drug development • Track record of successfully working within matrix of Commercial, Medical Affairs, and Market Access, as well as breaking down functional silos and managing complex trade-offs #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network We are Novartis. Join us and help us reimagine medicine.Division PHARMA Business Unit GLOBAL PRODUCT & PORTFOLIO STRATEGY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 United Kingdom Functional Area Commercial & General Management Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 360267BR Feb 17, 2023 Switzerland Job Description 13! The number of medicines Cardio Renal Metabolic diseases currently in development at Novartis. Novartis is deeply committed to transforming the lives of people living with cardiovascular, renal and metabolic diseases. We believe that anyone living with these conditions has the right to a life free from pain, free from symptoms and free from disease - this is our vision for the future. Our mission is to reimagine medicine to extend and improve people’s lives – and our overall company strategy to achieve this is to Focus Novartis as a leading medicine company powered by data science and advanced therapy platforms The Clinical Development Medical Director (CDMD) is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As CDMD, you will have oversight of the clinical development for the assigned programs and drive execution of the clinical development plan. In addition, you will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. Your responsibilities will include, but are not limited to: • Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program • Leading development of clinical sections of trial and program level regulatory documents • Driving execution the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable • Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues • Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas • As a medical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards • May work with NIBR (Novartis Institute of Biomedical Research/ Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you bring to the role: MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area (pediatric nephrology) ; Clinical practice experience 4 years (including residency) Minimum of 7 years of experience in clinical research or drug development Experience in an academic clinical research or industry environment spanning clinical activities in Phases I through IV required. 2 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry required. • Working knowledge of disease area is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports • Demonstrated ability to establish effective scientific partnerships with key stakeholders • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes • Previous global people management experience is preferred, though this may include management in a matrix environment. **Some restrictions to flexible working models may apply and will be discussed at interview if applicable Why consider Novartis? 769 million. That’s how many lives our products touched in 2020. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges.Division Global Drug Development Business Unit CARDIO-RENAL-METAB GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 354542BR Mar 23, 2023 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. We are looking for a Manager Internal Audit who will be a trusted partner for the business to improve governance, risk management, processes and our culture. You will get to engage with senior leaders of Novartis corporate functions and country organizations. You will also be able to further develop your skills and strengths that will help you to reach new heights in the profession in an inspired, curious and un-bossed organization. Your responsibilities include, but not limited to: • Plan, deliver and follow up from assurance and advisory projects in the markets and at the corporate level either as a team lead or team member. • Act as a cultural change agent, supporting assurance function with business partnering. • Manage knowledge and drive innovation to ensure high-quality, value-adding and digitally enabled audit execution. • Contribute to the digital transformation of the audit function to leverage the opportunities presented by current and new technologies and data across the organizations. • Bring a different perspective to review audit methodology projects and continuous im-provement initiatives. • Build and maintain key relationships with stakeholders, establishing a culture of engagement while adding value. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Bachelor's degree in business related field. Certification of IIA or working knowledge of GAAP and the IIA Standards for the Professional Practice of Internal Auditing is preferred. • 4 to 6 years relevant working experience in internal audit/advisory departments in a big four, in an IA boutique or consulting firm with focus on Pharma or the healthcare sector, OR a minimum of 6 years of experience in the business (e.g. commercial, general management, Finance) with a strong interest in internal audit • Good knowledge of SAP FI and CO modules, ACL, Tableau, Excel or other audit tool • Strong business acumen and knowledge of process management and/or business process optimization • Team-player with project management skills to collaborate effectively across a matrix and Ability to prioritize assignments, deal with interruptions, and meet deadlines in a fast paced and growth-oriented environment • Excellent communication and interpersonal skills including the ability to interact effectively with a wide variety of departments and leaders at all levels of the organization. • Strong analytical skills and ability to process and analyse large data size to identify trends and exceptions together with a positive attitude, pro-active and resourceful. • Proficient in English plus at least one other language desirable, like Russian, French, German, Spanish, or any Eastern European. Willingness to travel up to 30%Division CORPORATE Business Unit BUSINESS ASSURANCE AND ADVISORY Location Switzerland Site Basel Company / Legal Entity Novartis International AG Functional Area Audit & Finance Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358619BR Feb 23, 2023 Switzerland Job Description 1 company! That is the journey Novartis is on in its quest to extend and improve people’s lives through reimagining medicine. Group M&A is instrumental to achieve the 2nd pillar of NVS strategy: “Deliver Transformative Innovation” and is a priority from a capital allocation perspective. Externally sourced assets represent more than 50% of current pipeline and sales. Novartis has been a leading deal maker in the last 5 years. You will develop and execute on the M&A strategy, working closely with senior management, business franchises, and the newly formed Strategy & Growth function, being an integral part of the center of execution excellence (process, tactics and valuation) Key Responsibilities: • Work closely with senior management to understand key business objectives • Build collaborative relationships with key stakeholders to ensure continuous development of M&A strategic roadmap • Coordinate interactions across firm including key corporate functions (tax, legal, BPA, finance) • Provide support services to the business to assess M&A opportunities • Build relationships with external parties to facilitate implementation of M&A strategy (potential targets, legal advisors, banks) • Proactively develop insights on competitors with respect to their M&A strategy • Lead M&A projects to deliver first-class execution of mergers, acquisitions, joint ventures, strategic alliances and other business combination transactions • Provide project management and holistic oversight during execution of projects (including due diligence, valuation, negotiations, key documentation, preparation of groundwork for post-merger integration) Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Advanced University Degree/MBA (discipline with analytical content) • 10+ years M&A transaction experience in the pharma/biotech industry, especially in a project leadership capacity • Strong Investment Banking background with an In-depth knowledge of Corporate Finance • Extensive negotiation experience • Excellent analytical skills with conceptual thinking capabilities • Strong planning skills including the ability to identify critical items in advance and proactively address them in coordination with top management • Strong executive presence and interpersonal skills with ability to challenge constructively Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network[SS(1]Division CORPORATE Business Unit Global Corp. Finance Location Switzerland Site Basel Company / Legal Entity Novartis International AG Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 368137BR Mar 22, 2023 Switzerland Job Description 236 million! That’s how many lives our products touched in 2022. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! The Global Program Clinical Head (GPCH) is the global clinical leader responsible for one or more clinical programs across indications, involving one or multiple compounds. The GPCH owns the risk benefit assessment for the program(s), and as the leader of Global Clinical Team(s) (GCT) is accountable for the design, implementation, and execution of a clinical development program(s) to support decision milestones, regulatory requirements and market access. The GCPH may contribute to disease area strategy. The role reports into the Clinical Development Head. Your responsibilities will include: •Leads the GCT, represents Clinical Development on the Global Program Team (GPT) •May serve as the Clinical Development Representative on NIBR clinical/project teams to drive transition of pre-PoC (Proof of Concept) projects to Development Decision Point (DDP) •May support Business Development & Licensing (BD&L) activities •Post-Development Decision Point, leads the development and execution of the clinical strategy. Develops an endorsed Integrated Development Plan (IDP) in line with the Target Product Profile (TPP) which is designed for successful global regulatory approval/market access for one or multiple treatment indications and/or multiple programs •Leads the creation of clinical components of key documents (e.g., Clinical Trial Protocols (CTPs), Investigator’s Brochures, Clinical Study Reports (CSRs), regulatory documents including maintenance of product licenses, registration dossiers, value dossiers, pharmacoeconomic dossiers) with high quality and consistency with IDP and TPP. Supports registration, market access, commercialization, and maintenance of product licenses (e.g., Core Data Sheet, Periodic Safety Update Report, clinical benefit-risk assessment for license renewals) for the compound(s) •Together with Patient Safety, ensures continuous evaluation of drug safety profile, including safety monitoring of clinical studies and signal detection from post-marketing surveillance. Serves as a core member of the Safety Management Team (SMT) •As the medical expert, leads interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring committees, advisory boards, patient advocacy groups), internal stakeholders (e.g., Research, Translational Medicine, Global Medical Affairs (GMA), Marketing, Health Economics & Outcomes Research), and internal decision boards. **Some restrictions to flexible working models may apply and will be discussed at interview if applicable Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • MD or equivalent (required) • PhD (preferred) • 5 years professional experience as MD and a minimum of 10 years of experience with clinical drug development in an industry environment spanning clinical activities in Phases I through III/IV and experience with leading submission dossiers (required) • Ideally a Board certified Nephrologist OR extensive (> 5 years) experience in clinical development withing the Nephrology Therapeutic area • Advanced knowledge of assigned therapeutic area required, with the capability to innovate in clinical development study designs that provide relevant evidence to decision-makers, and to interpret, discuss and present clinical trial or section program level data • Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, and regulatory/clinical development process required • Demonstrated ability to establish strong scientific partnership with key stakeholders • Demonstrated leadership and management skills with a documented track record of delivering high quality projects/submissions/trials in a global/matrix environment (including remote) in pharmaceutical or biotech industry Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit CARDIO-RENAL-METAB GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 367781BR Mar 22, 2023 Switzerland Job Description 200+! This is the current number of programs in clinical development at Novartis. Many of these projects, which include new molecular entities as well as additional indications and different formulations for marketed products, are for medicines that could significantly advance treatment standards for patients worldwide. As an experienced subject matter expert in the application of milling technologies for the preparation of drug substances and drug products, you will support a New Chemical Entities project portfolio, focusing on small molecules. As part of a Materials Science team, you will scientifically drive the development of laboratory processes and support the transfer of processes to pilot and commercial manufacturing facilities. You will also play a key role in strengthening scientific excellence at the interface between drug substance and drug product development and will bring with you a deep understanding of both particle and powder properties, which you can apply to successfully support project teams operating in both early and late phase development. In addition, you will work alongside crystallization and solid state experts as well as formulators to optimize the physical properties of a drug substance for subsequent use in drug product development. Your key responsibilities will include: Ensure the development of robust sieving and milling operation steps for integration into both the chemical and pharmaceutical manufacturing chains Transfer of processes to and between pilot plants and commercial facilities, both internally and externally Drive discussions relating to powder and particle properties as a subject matter expert, and support interpretation of appropriate analytical results Drive cross-team and cross-functional knowledge exchange in the areas of milling and sieving and more broadly (particle science, powder properties) through coaching to increase the skill base relating to Materials Science Be an advocate for strengthening the interface between drug substance and drug product development, both within the Materials Science unit and within Project Teams Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Ideal requirements: • PhD in relevant scientific field (e.g. particle technology, (mechanical) process engineering, materials science) • Minimum 3 years of successful pharma industry experience as a subject matter expert in milling (development and/or manufacturing setting, ideally both). Familiarity with HSE for powder processing and GMP requirements would be advantageous • In-depth technical knowledge of appropriate process technologies used to achieve, in particular, particle size reduction during the manufacture of both drug substances and drug products. Specifically, dry operations such as sieving, milling, micronisation and wet operations such as wet-media milling. • Profound knowledge in fundamental powder (and suspension) characterization technologies (e.g. laser light diffraction, ring shear tester, analytical centrifugation, dynamic vapor sorption, dynamic light scattering, zeta potential, etc.) • Experience in the stage appropriate requirements in drug substance and drug product technical development from early to late stage development as well as process transfers to commercial facilities • Strong communication, negotiation, presentation, technical writing, coaching skills. Desire to help associates grow in new and existing roles . • Interdisciplinary thinking and strength in cross-functional collaboration • Experience in working within complex stakeholder environments with extensive interfaces • Excellent planning and work prioritization skills. • English (fluent) required. German desirable. Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 368089BR Mar 22, 2023 Switzerland Job Description 200+! This is the current number of programs in clinical development at Novartis. Many of these projects, which include new molecular entities as well as additional indications and different formulations for marketed products, are for medicines that could significantly advance treatment standards for patients worldwide. As an experienced subject matter expert in solid state and particle engineering for the preparation of drug substances, you will support a New Chemical Entities project portfolio with a main focus on small molecules. As part of a Materials Science team, you will scientifically drive the selection and the characterization of the appropriate solid form as well as the development of laboratory crystallization processes for the isolation of active pharmaceutical ingredients (API) and support the transfer of these processes to pilot and commercial manufacturing facilities. You will also play a key role in strengthening scientific excellence at the interface between drug substance and drug product development and will bring with you an understanding of solid state analytics, particle and powder properties to support project teams operating in both early and late phase development. In addition, you will collaborate alongside experts in the application of API finishing technologies for the preparation of drug substances and drug products as well as formulators to develop, assess and optimize the physical properties of a drug substance for subsequent use in drug product development. Your key responsibilities will include: • Ensure the appropriate selection, development, and characterization of solid forms of an API during early and late phase product development. • Develop robust crystallization manufacturing processes to deliver drug substances in line with drug product needs. • Transfer of processes to and between pilot plants and commercial facilities, both internally and externally. • Drive discussions relating to particle and powder properties as a subject matter expert and support interpretation of appropriate analytical results. • Drive cross-team and cross-functional knowledge exchange in the areas of API particle design and characterization (eg. finishing technologies, solid state characterization, crystallization development, powder properties) through coaching to expand the skill base relating to Materials Science. • Be an advocate for strengthening the interface between drug substance and drug product development within the Materials Science unit, project teams and across functions. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Ideal requirements: • PhD in relevant scientific field (e.g. particle technology, chemical engineering, materials science, physical chemistry) • Minimum 3 years of successful pharmaceutical industry experience as a subject matter expert in API solid state and particle engineering, including crystallization processes in a technical development setting. • Broad scientific and technical knowledge in appropriate analytical technologies used for API and powder characterization (e.g. x-ray powder diffraction, thermal analysis, laser light diffraction, dynamic vapor sorption, dynamic light scattering) • Experience in the stage appropriate requirements in drug substance and drug product technical development from early to late stage development as well as transfers to commercial facilities. • Strong communication, negotiation, presentation, technical writing, coaching skills. Desire to help associates grow in new and existing roles. • Interdisciplinary thinking and strength in cross-functional collaboration. • Experience in working and managing complex stakeholder environments across line functions. • Excellent planning and work prioritization skills. • Familiarity with GMP requirements would be advantageous. • English (fluent) required. German desirable. Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 362426BR Feb 20, 2023 Switzerland Job Description 365 Tage im Jahr arbeitet unser globales Produktions- und Liefernetzwerk, um sicherzustellen, dass unsere Patienten die Behandlungen erhalten, die sie für ein längeres und gesünderes Leben benötigen. Als Equipment Specialist in der Medien- und Pufferherstellung bist Du für die Ausführung von zugewiesenen Herstellungsaufgaben und -tätigkeiten gemäss dem Produktionsplan zuständig, um die rechtzeitige Produktion des Produkts in Qualität und Quantität gemäß den einschlägigen GMP-, Sicherheits- und Umweltrichtlinien zu ermöglichen. Ihr Verantwortungsbereich: • Selbständiges Durchführen und Protokollieren sämtlich zugewiesener Tätigkeiten gemäss dem Produktionsplan und der gültigen GMP-, Arbeits-, Betriebs-, Umwelt- und Sicherheitsanweisungen und –richtlinien • Rechtzeitige und fehlerfreie Überprüfung der Herstelldokumentationen • Verantwortung für die Sauberkeit und Ordnung des Produktionsbereichs (Reinigung, Ordnung, 5S, etc.) • Einhaltung und Durchsetzen der Gesundheits-, Sicherheits- und Umweltregeln und -richtlinien (HSE) • Probenahme, Aliquotierung, Verteilung und Durchführung von prozessbegleitenden Kontrollen • Delegierte Umweltüberwachung für Reinräume und delegierte Probenahmen von Reinstwasser und Reindampf durchführen • Im Störfall sofortige Massnahmen ergreifen, Auffälligkeiten an die Manager; Experten und operative Qualitätssicherung melden • Sicherstellung/Überwachung einer ordnungsgemässen Funktionstüchtigkeit der Anlagen, um frühzeitige Anzeichen von Anomalien zu erkennen. Im Störfall geeignete Massnahmen ergreifen. • Exzellente Dokumentation der Massnahmen, gemäss den GMP-Vorschriften Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie für die Position mitbringen • Abgeschlossene Chemie- und Pharmatechnologie-Ausbildung oder adäquate Ausbildung mit mehrjähriger Berufserfahrung in den Bereichen Chemie / Lebensmittel / Arzneimittel / Biotechnologie / aseptische Herstellung oder Entwicklung. • Bereitschaft Schichtarbeit • Teamplayer mit gutem Teamgeist • Fähigkeit Probleme zusammenzufassen und Lösungen vorzuschlagen • Sehr gute Deutschkenntnisse in Wort und Schrift. Englischkenntnisse sind gewünscht. • Beherrschung der GMP-Standards • Gute Kenntnisse in MS Office und Prozessleitsystemen • Gutes technisches Verständnis • Beherrschung der relevanten Systemsteuerungen (SAP, WinCC, Lucullus) Warum Novartis? Im Jahr 2021 wurden fast 800 Millionen Menschen mit Medikamenten von Novartis behandelt. Wir sind stolz darauf, aber wir wissen auch, dass wir noch viel mehr tun können, um das Leben der Menschen zu verbessern und zu verlängern. Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können. Wir glauben, dass ein vielfältiges, gleichberechtigtes und integratives Umfeld neue Arbeitsweisen inspiriert. Wir glauben, dass unser Potenzial in einer Kultur ohne Zwänge, die von Integrität, Neugier und Flexibilität geprägt ist, gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mutig zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stell dir vor, was du hier bei Novartis tun könntest! Tritt unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu deiner Erfahrung oder deinen Karrierezielen passt, du aber in Kontakt bleiben möchtest, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, dann tritt dem Novartis Netzwerk hier bei: https://talentnetwork.novartis.com/network Werden Sie Mitglied in unserem Novartis Netzwerk: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/network Wir sind Novartis. Kommen Sie zu uns und denken Sie Medizin mit uns neu.Division Novartis Technical Operations Business Unit CONTRACT MANUFACTURING Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work Yes Apply to JobAccess Job Account

Job ID 367778BR Mar 21, 2023 Switzerland Job Description 200+! This is the current number of programs in clinical development at Novartis. Many of these projects, which include new molecular entities as well as additional indications and different formulations for marketed products, are for medicines that could significantly advance treatment standards for patients worldwide. As an experienced technical laboratory expert in the field of dry and wet milling processes you will perform scientific experiments with active pharmaceutical ingredients (APIs) to support the development of drug substance (DS) and certain drug product (DP) processes. You will be responsible for the set-up, cleaning and maintenance of the lab equipment and will perform various analytical analyses to collect and interpret experimental results. Applying your professional experience, you will also coach peers and support the transfer of milling processes to pilot or production sites. Key Responsibilities • Plans, performs and documents scientific experiments in the field of dry milling/sieving and wet media milling. • Support the growth of associates (peers) in the areas of milling and sieving through coaching to increase the technical skill base within a Materials Science team • Performs analytical measurements with different instruments (e.g. analytical centrifugation, rheometry) • Provides documentation of raw data, evaluation and interpretation of results. • Supports transfer of processes developed in the laboratory to pilot scale or production facilities Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Ideal Requirements • Technical education in appropriate or related discipline (e.g. ‘Chemie- und Pharmatechnologe’) • Practical experience in operating diverse milling technologies (e.g. wet media milling, pin milling, jet milling) • Practical experience in the set-up, cleaning and maintenance of relevant equipment, including thorough awareness of HSE requirements • Practical experience in executing appropriate powder analytical methods (e.g. particle size, rheology) • Industrial experience working in a pharmaceutical development or pharmaceutical manufacturing environment is desirable • Good collaboration and communication skills. Able to plan and prioritise work schedule. • Fluent in English and/or German Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 368122BR Mar 21, 2023 Switzerland Job Description 20 petabytes of data – this is how much data we generated at Novartis across 100s of clinical trials, pre-clinical studies and drug candidate discovery and development projects! All waiting for you to unlock the next breakthrough in medicine. Do you want to apply your data science expertise to the life sciences? As a Data Science Academy Program fellow, you will join Novartis’ Translational Medicine Unit to help us to unleash the power of data science for drug discovery and development. During your 24 months journey, you will rotate in three departments of our Unit and apply your skills to challenges in translational medicine. Who are you? You are a passionate and curious data scientist early in your career, eager to bring creative solutions and a novel perspective to biology’s most daunting challenges on our journey to reimagine medicine. Working alongside dedicated physicians and scientists, our data scientists provide the analytical insights that drive translational success. You will be - Working as a member of cross-functional teams - Communicating regularly with collaborators and assisting with answering their questions with the data and analytics - Using and developing novel machine learning and statistical techniques and apply them to different data modalities - Generating insights related to discovery, pre-clinical and clinical projects and inform team on their decision making - Presenting project outcomes to technical and non-technical audiences - Participating in drug discovery training courses - Contributing to research papers and publications Duration: 24 months, planned start: 1 July 2023 2023 Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements MSc or PhD in computational sciences, physics, mathematics, economics, computational biology, machine learning, data science or related field • Expert knowledge of programming in R or/and Python • some experience in the field of data science • Strong grasp of statistics and machine learning • Experience with reproducible data science tools and practices • Excellent communication skills and ability to translate analytical concepts for diverse audiences and stakeholders (English is our primary language) 743 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division NIBR Business Unit Translational Medicine Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 360413BR Jan 23, 2023 Switzerland Job Description Millions! Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. Lead industry-leading Therapeutic Area (TA) Policy strategy and execution, partner very closely and directly contribute to the success of key TAs/assets. Position Novartis as a trusted collaborator and partner, leading partnerships with healthcare system stakeholders relevant for TAs (e.g., academics, therapeutic area-specific policy and advocacy groups, professional societies, payors) in partnership with Global Public Affairs and Patient Engagement across global, regional, and key priority market settings. Establish strategic partnership with TAs and strong collaborations with Access, HEOR and HCS colleagues to produce fit-for-purpose value propositions, evidence, funding, and access strategies that will be required for robust HCS partnering. Major responsibilities: Your responsibilities include, but are not limited to: • Develop and implement transformative TA policy solutions serving strategic therapeutic areas (TAs) with focus on key brands and priority market and one BI market • Champion public affairs customer- and HCS-centric perspectives across the Value & Access team, ensuring both a holistic access strategy and achievement of broader HCS goals. • Based on a strong external network, build out space as recognized global thought leader TA policy work, build de novo therapeutic area-specific partnerships and coalitions as required • Provide therapeutic area-specific thought leadership for Global Public Affairs led engagements that support healthcare system and policy change conducive to the TA • Partner with the TAs cross functional teams to prepare favorable market conditions for priority pipeline assets • Provide TA insights in support of broader Novartis Corporate public affairs and market access workstreams, provide insights on business impact of broader corporate policy work/global public affairs (i.e., biosimilars, environmental policy, CSR) • Align and support implementation of deliverable with cross-functional advocacy partners, e.g., patient engagement, Comms, Medical and Global Public Affairs Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Minimum Requirements Minimum requirements: What you'll bring to the role: • Every candidate who is considered must have the qualifications described here. A candidate without these qualifications will not be considered or presented to the hiring manager • Advanced degree in law, public health policy, health economics, political science or equivalent • 5+ years in policy or advocacy related roles, either in leading industry player or policy setting body such as government, IGOs, trade group etc. • 7+ years in healthcare related roles, preferably focused on pharmaceutical policy. • Min. 5 years of senior roles in global/product public affairs, market access or related positions in a multinational pharmaceutical company • Extensive experience representing the pharmaceutical industry in policy fora, with track record of measurable business impact. • Experience with designing and executing market shaping strategies across multiple geographies. Desirable requirements: • Highly preferred: 10+ years in policy or advocacy related roles, either in leading industry player or policy setting body such as government, IGOs, trade group etc • Highly preferred: Significant (3+ years) and recent (post 2015) US in-market experience: includes working in the US market with the local US customers, US health care systems / systems of care, US payors / accounts, US market strategy etc. #transformingforgrowth Why consider Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision PHARMA Business Unit GLOBAL PRODUCT & PORTFOLIO STRATEGY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Market Access Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 368239BR Mar 21, 2023 Switzerland Job Description Be at the front line for innovative pharmaceutical products that reach patients in more than 150 countries. As part of Pharmaceutical Development (PHAD) you can make a difference to millions of patients around the world by continuous development of new chemical entities and upcoming exciting commercial products. Position Purpose: we aim to develop and implement innovative pharmaceutical technologies (solid oral, topical, parenteral, ophtalmic and inhalation dosage forms containing small molecules NCEs). As a Master Student or a training placement for 6 months, within this innovative environment you will contribute to elaborate pharmaceutical processing technologies and to develop pharmaceutical formulation know-how for novel technologies. Your work will be focused around the research, development and characterization of dosage forms and their components, and how this translates to the production of innovative pharmaceuticals. Duration: 6 months Start date: November 2023 Tasks / Responsibilities: There are a range of projects available which may cover any of the following areas: • Development of novel dosage form technologies • Feasibility trials to understand the impact of new technologies • Characterization of material properties and linking to process performance • Process development activities and assess process performance • Build related models interconnecting material properties and process performance • Compare model prediction with process performance • Summarize and present results in internal meetings Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Master Student in e.g. Pharmacy, Pharmaceutical Engineering, Chemical Engineering, Pharmaceutical students during their practical year (after second state examination) • Special interest in formulation, pharmaceutical technology/processing and/or physico-chemical properties /pharmaceutical material sciences (e.g. powder characterization) • Ability to work in multidisciplinary teams in an international environment • Organizational, and scientific skills including curiosity and planning and execution of lab work • Proficiency in English, German skills are advantageous Desired requirements: • strong communication and presentation skills • Familiarity with Microsoft Office, additional packages e.g. Minitab would be advantageous 743 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Global Drug Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 361448BR Feb 07, 2023 Switzerland Job Description Clinical Operations Program Head 100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medicine – imagine the impact you could have as Clinical Operations Program Head! #GCO This role will be part of the GCO Selection University approach. If you wish to apply for any more Selection University positions, please make sure you do so within the same day to ensure your applications can be reviewed jointly by the selection panel. The Clinical Operations Program Head (COPH) is accountable to deliver data-driven, actionable operational and strategic insights for execution of a clinical development program and all associated trials by representing GCO at the Global Clinical Team (GCT) as well as at the Global Program Team (GPT). The COPH actively contributes to the GPCH’s and GCT’s strategic objective to achieve their own overall accountability for delivering the clinical program. The COPH provides the operational perspective to the Clinical Development Plan and to trial protocol design, ensuring that GCT/GPTs are aware of operational considerations and options, and that these are adequately reflected in planning. The COPH is the single point of contact for a trial/program within GCO and partners closely with key members of the GCT/GPT such as GPCH, GPH and other key communities to ensure best collaboration with operations to drive overall success of our programs and trials. The COPH leads the GCO sub-team to determine the GCO operational input to planning prior to any given development tollgate and to prepare the Operational Execution Plan (OEP), which is authored and owned by the COPH. The OEP incorporates both data-derived insights as well as country insights which enable informed decision-making, identify complexity, enable the generation of risk mitigation plans to reduce chances of delays, allow easier adaption of actions, and ensure transparency of the GCO operational position and the downstream delivery of program and trial milestones. Experienced leader guiding members of the organization through the GCO organizational evolution, the evolution of new “product aligned” ways of working and of our overall culture. He / she champions a product oriented agile mindset, fostering a culture of experimentation combined with accountable delivery and overall high performance. Your Key Responsibilities: 1. Accountable for the operational delivery of the clinical development program and is responsible for the overall operational execution of the clinical program and related trials, as aligned with the IDP/CDP. 2. Single GCO point of contact for assigned clinical development program and related trials. 3. Key partner to GPCH during strategy, planning and execution stage of the program and related trials ensuring that the clinical science and strategy are consistently harmonized with an operationally feasible approach within the OEP-defined operational boundaries, so that the trials generate reliable information to answer the research questions and support decision making while protecting study participants. 4. In partnership with GCPH and other GCT members, actively offer operational insights and options to contribute to the program and trial strategy, in particular with respect to study design and protocol optimization and timelines planning. 5. Leads the GCO sub-team to ensure the creation of best-in-class OEPs and to ensure that progress of the assigned programs and trials is on track and that operational risks are identified and mitigated proactively. The COPH further leads the GCO sub-team to ensure monitoring of the status of the progress of the clinical trials in line with the OEP and to deploy mitigation measures whenever needed to ensure overall trial success. 6. Leads the GCO sub-team taking accountability for the success of the team and of each team member by implementing “agile” and “product-oriented” ways of working. 7. Holds accountability for the operational delivery of the assigned program and related clinical trials and for all related strategic planning, prioritization of activities within that program. 8. Is a key contact to senior leaders in GCO and beyond. Empowered to manage stakeholders, resolve conflict, and facilitate agreements Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What You’ll Bring to the Role: • Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred (PhD/MD/ PharmD/ Masters). • Fluent English (oral and written) • 10 or more years of experience in pharmaceutical clinical drug development. • Experience in managing associates globally and in management in a matrix organization. • Proven ability to lead cross functional matrix teams applying product-oriented agile ways of working. • Strong leadership, interpersonal and problem-solving skills. High resilience and ability to advocate and implement new ways of working. • Has ability to understand data and insights with ability to communicate this succinctly and accurately • Extensive knowledge of clinical development processes, preferably extensive knowledge of Novartis late-stage development processes or high likelihood to develop it within 6 months after appointment. • Proven ability to lead in times of organizational transformation and to lead across organizational boundaries. • Strong organizational awareness and stakeholder management skills. • Strong knowledge of therapeutic area or high likelihood to develop it within 6 months after appointment. Strong matrix management skills for bridging stakeholders (business, scientific, technical) • Strong relationship-building skills; can influence, negotiate with and motivate executive leadership • Strong tolerance for ambiguity, willingness to adapt, willing to speak-up and challenge • Embraces a culture of diversity, inclusion, quality, innovation and driving forward with integrity at all times Why Consider Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity, and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!Division Global Drug Development Business Unit GDO GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 India Alternative Location 2 Ireland Alternative Location 3 United Kingdom Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 359036BR Feb 21, 2023 Switzerland Job Description 800 million people! That’s the number of people we reach globally. Novartis is reimagining medicine to improve and extend people’s lives, and we are finding innovative ways to expand access to our latest treatments. The focus of the SIA role is to protect Novartis associates, estate, products, intellectual property, reputation and patients globally from the threat of criminal actions emanating from: cybercrime, the falsification and counterfeiting of Novartis products, attacks against travelling associates, unscrupulous vendors/counterparties, ‘insider’ threats regarding fraud and corruption, and asymmetric threats from extremism, extortion, blackmail, bribery, indiscriminate terrorism and other criminal activity. The Senior Intelligence Analyst (SIA) is responsible for deputizing in the absence of the GSIU Director for the day-to-day operational management of the GSIU, in particular the management, assignment and quality assurance of intelligence requests and reporting. The role additionally leads the operational management of the Novartis global travel security program and cross-function collaboration in root cause analysis for internal misconduct and other uses of this structured analytical technique. The SIA acts as point of contact for stakeholders and coaches team members in complex analysis. Your responsibilities include, but not limited to: • Deputize in the absence of the GSIU Director, leading the day-to-day operational management of the GSIU. To include quality assurance of intelligence reports, negotiation of requests for intelligence re-ports and tasking of GSIU analysts. Provide to the GSIU, and wider Global Security community peer-to-peer coaching and training, as well as on-boarding of new team members. • Drive innovation to the analysis and understanding of root cause analysis and contribute to the wider Global Security training around its application. Lead on behalf of Global Security the cross – functional training of root cause analysis to identify causes of internal misconduct. • Lead the global travel security and travel incident response program and advise/coach team members in complex analysis. • Manage the process of global country risk mapping assessments across all regions through the collation of intelligence requests, procurement process for vendors, vendor and stakeholder management and quality review of the final product. • Alongside the GSIU Director manage knowledge and drive innovation within analysis to ensure high-quality, value-adding intelligence products • Act as the single point of contact for external sources and agencies - to build a detailed intelligence picture regarding threats to Novartis. • Work on assigned priorities and to an agreed plan, manage the ‘intelligence cycle’ through the systematic collection, collation, evaluation, interpretation and analysis of information and process this in-to timely, accurate, and relevant intelligence • Produce and work on complex, high quality threat assessments, security alerts, management briefings, country risk assessments, multi-media presentations and other relevant security and awareness products for dissemination to relevant audiences across Novartis. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • University degree in intelligence management or international corporate security or equivalent. • + 10 years who is considered an expert threat intelligence analyst. Strong project management track record, ideally in a complex international company. • Proven experience and track record in intelligence work applicable to role is essential: e.g., counterterrorism/ counter-extremism/ counter-narcotics / criminal investigations /other relevant area. • Experience in a Military/law enforcement/customs/security intelligence/commercial intelligence background. • Very good command of English (written and spoken), other languages desirable. Why consider Novartis? 766 million. That’s how many lives our products touched in 2021 and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis Imagine what you could do at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network We are Novartis. Join us and help us reimagine medicine.Division CORPORATE Business Unit BUSINESS ASSURANCE AND ADVISORY Location Switzerland Site Basel Company / Legal Entity Novartis International AG Functional Area Legal & Intellectual Property & Compl. Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 368110BR Mar 21, 2023 Switzerland Job Description 74! The number of medical device projects in Novartis. Without a safe, user friendly, high-quality drug delivery system our patients cannot take their medicine. Among the developed drug delivery products, some are based on technologies that are directly created by Novartis. In this regard, Novartis is responsible for the complete engineering work until market access and also during the market life of the product. Device Technology department in Basel needs you to support this effort by creating the appropriate documentation which records all simulation know-how for product development and optimizing the methods. You will be conducting 3D-simulations for design verification, collecting data or running tests to validate the simulation models, that allows the development team to not only have full understanding or major design & process parameters, but at the same time able to predict and reduce Defect Parts Per Million at End Of Line. In addition, you will have the opportunity to participate and gain experience in medical device development as well as contributing to the digital strategy. Your responsibilities include, but are not limited to: • Document and optimize existing simulation method • Validate simulation model with test results • Conduct Sensitivity Analysis for Robust Design Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Master Student in Engineering, Biotechnology or Life Science or Computer Science • Quick learner, quality focused, good communication and collaboration skills, autonomous and self-driven. • Knowledge in simulation and associated tools (Ansys LS-Dyna, Fluent...) • English both spoken and written is a must, German and French a plus. Desirable requirements (optional): • Medical device knowledge through university studies or direct work experience. • Knowledge of regulatory standards for medical devices and/or combination products. • Knowledge in statistics Why Novartis? 743 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Global Drug Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 368115BR Mar 20, 2023 Switzerland Job Description 74! The number of medical device projects in Novartis. Without a safe, user friendly, high-quality drug delivery system our patients cannot take their medicine. Among the developed drug delivery products, some are based on technologies that are directly created by Novartis. In this regard, Novartis is responsible for the complete engineering work until market access and also during the market life of the product. Device Technology department in Basel needs you to support this effort by creating the appropriate documentation which records all design choices and their links to product characteristics in order to manage future changes and improvements. Being integrated into the design team, you’ll be collecting and generating evidences supporting the design of our new connected auto-injector which includes mechanical functions. Understanding the details of the choices made to increase the performances and the manufacturability will be key in these activities. In addition, you will have the opportunity to participate and gain experience in medical device development [in compliance with the EU Medical Device Regulations and ISO 13485 as well as US regulations 21 CFR Part 4 and 21 CFR Part 820] as well as contributing to the digital strategy. Your responsibilities include, but are not limited to: • Collect and understand the reason of the design choices • Generate missing evidences via CAD, tolerance analysis, simulations and testing. • Write reports aligned with the Good Documentation Practice rules • Support the team with proposals and solutions for efficient and sustainable recording of the generated documents Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Minimum Requirements Master Student in Engineering, Biotechnology or Life Science or Computer Science • Quick learner, quality focused, good communication and collaboration skills, autonomous and dedicated. • Knowledge in mechanics and associated tools (e.g.CAD, FEA) • English both spoken and written is a must, German and French a plus. Desirable requirements: • Medical device knowledge through university studies or direct work experience. • Knowledge of regulatory standards for medical devices and/or combination products. • Knowledge in statistics 743 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Global Drug Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 362812BR Mar 21, 2023 Switzerland Job Description 766 million! That's how many patients' lives were touched by our products in 2021. At Novartis, we are reimagining medicine to improve and extend people's lives. We use innovative science and technology to address some of society's most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. How can we continue to advance our science to help even more patients in need? We believe the answers are found when curious, courageous, and collaborative people are empowered to ask new questions, make bolder decisions, and take smarter risks. We are welcoming a passionate Finance enthusiast, with the desire to learn, grow and develop his / her professional career within our company and to gain their first financial professional experience. If you found yourself in this description, join us in the role of Junior BPA Finance Basel and start your financial career development in NVS! Major accountabilities: - you will be responsible for planning and variance analysis as well as reporting templates and process enhancement for management cash flow and other income and expenses of the reporting entities that form the Region ‘Parent Companies’ Management Cash flow: o Evolution and drivers of balance sheet accounts (trade receivables & payables, other current assets and liabilities) with focus on royalties, divestments, milestones and taxes o Related key performance indicators: days payable and receivable outstanding o Based on input from stakeholders across multiple entities and functions OIE: o Other income and expense items of IM business unit o Collection and analysis of - launch provision data in close collaboration with NTO & GDD - profit transfer data in close collaboration with Alliance managers Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements - finished University (Financial field) - Experience with Microsoft Office, SAP, FcRS, BPC and QlikSense is asset Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division PHARMA Business Unit Global Finance&Admin Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Audit & Finance Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 366305BR Mar 21, 2023 Switzerland Job Description 2023 will see Sandoz become a standalone organization! As a global market leader in Generics and Biosimilar medicine, Sandoz is stepping forward from a position of strength! Those joining Sandoz in the coming months will help shape the future of the company, it’s growth, innovation, culture and how Sandoz impacts the lives of millions. These will be careers with genuine impact! This is one such role! Are you ready to make a difference? Job Summary/Purpose : - Provide the strategic and technical leadership for global Supply Chain in all Good Distribution Practice (GDP) related matters, to ensure that all aspects of the business comply with legal and regulatory requirements and the Novartis Corporate Quality Manual - Lead global Supply Chain operations in strategic projects from QA point of view - Provide high standard Quality Assurance expertise during preparation and negotiations of supply and commercial agreements to ensure correctly designed and implementable quality related processes - Prepare and negotiate Quality Agreements with internal and external partners. - Sign Quality Agreements and other documents within area of responsibilities on behalf of Sandoz AG - The holder of the position is the Responsible Person (“Fachtechnisch Verantwortliche Person”) and / or Responsible Person and Swissmedic license holder (verantwortliche Person, Betäubungsmittelgesetz BetmG) for the handling of narcotics at Sandoz AG, Basel.according to the Swiss Regulation on Authorizations in the Area of Medicinal Products (Verordnung über die Bewilligungen im Arzneimittelbereich, AMBW) for Sandoz AG Your Key Responsibilities Your responsibilities include, but not limited to: - Ensure that all global aspects of handling and distribution of pharmaceutical products at the Swiss Hub and all STO sites and affiliates comply with the Sandoz Quality Manual, regulatory and legislative requirements - Has full authority to take decisions independently with regards to the following responsibilities: - Responsible Person (“Fachtechnische Verantwortliche Person”) according to the Swiss Regulation on Authorizations in the Area of Medicinal Products. Responsible for maintaining the Sandoz AG distribution licenses. - and/or the Responsible Person and Swissmedic license holder (verantwortliche Person, Betäubungsmittelgesetz BetmG) for the handling of narcotics at Sandoz AG, Basel. - Ensures an adequate Quality Management System (QMS) is in place for Sandoz AG has full oversight on the QMS for the related activities. Ensures, in particular, that an adequate Market Action procedure is in place and is the main point of contact at Sandoz AG in the event of any Market action. Act as a worldwide contact and expert regarding all questions internal or external (e.g. from Health Authorities) and issues concerning Good Distribution Practices and related Novartis standards - Ensure continuous improvement of quality relevant processes within area of responsibility - Act as subject matter expert for Sandoz AG in global/local projects where applicable - QA Lead to assigned projects in Global Supply Chain to drive projects to successful completion ahead of time and on quality - Support defining Sandoz, SCM QA strategy to ensure compliance of Swiss Hub and all STO sites and country organizations with all aspects of GDP (e.g. management of Health Authority licenses, risk management, deviation handling, transport monitoring, return of goods and recall management) - Provide high standard and on time quality expertise during preparation and negotiations of supply and commercial agreements to ensure correctly designed and implementable quality related processes - Prepare and negotiate Quality Agreements with internal and external partners. Sign Quality Agreements and other documents within area of responsibilities on behalf of Sandoz AG. - Define QA strategy and design the QA process for GDP global best practices and lessons learnt sharing across Novartis - Support GxP audits (self-inspections and audits of third parties, e.g. partner warehouses) and prepare/support/lead Health Authority inspections (e.g. FDA, Swissmedic, EMA) - Maintain current knowledge of regulatory and legislative requirements and trends related to GxP and specifically to GDP in order to ensure an expert advice and appropriate quality technical support on all quality related distribution activities. - Handling of transport deviations including recording, investigating, evaluating and answering to customers. Use of the Transport Deviation tools (1QEM, AQWA, Trackwise). - Support deviation handling within Global Supply Chain Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: - University degree in life sciences, preferably in pharmacy or chemistry or equivalent - Minimum 12 years of experience in the pharmaceutical industry out of which 8 years in a leading quality role. - Deep leadership knowledge and experience in GxP, preferably GDP (Good Distribution Practices). - Extensive knowledge of the Sandoz products and business processes experience in leading global teams. - Experience in communication with manufacturing sites and market authorization holders. - Experience in communication with international project teams. - Strong experience in pharmaceutical project management. - Fluent in written and spoken English and German #Orbit Why Sandoz? 500 million patients were touched by Sandoz generic and biosimilar medicines in 2021 and while we’re proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world. How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could achieve here at Sandoz! Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Sandoz Network : If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Sandoz and our career opportunities, join the Network here: https://talentnetwork.novartis.com/sandoztalentpoolDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Basel Company / Legal Entity Sandoz AG Functional Area Quality Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 363261BR Mar 21, 2023 Switzerland Job Description 20 years and 2 million-years of patient data waiting for you to unlock the next breakthrough in medicine ! At Novartis, we are reimagining medicine to improve and extend people's lives. We have one of the most diverse product pipelines in the pharmaceutical industry and performance-driven professionals are bringing innovative medicines to life. The department of Pharmacometrics at Novartis will have multiple internship positions available. Timing: Flexible from April to September Duration: The internship is expected to last 3 months Your responsibilities: • This internship will focus on longitudinal disease progression and drug effect (PKPD) models targeting the support for dermatology portfolio at Novartis. Various clinical problems will give the candidate a hands-on exposure to questions to be addressed in drug development • Work on your own Pharmacometrics modeling project under the guidance of senior-level quantitative scientists • Analyze data from various sources (e.g., clinical trials, competition database) • Attend seminars and other activities to enhance the understanding of the drug development process • Present your project results to quantitative scientists and other stakeholders • This internship will provide motivated students with exposure to the pharmaceutical industry, and with the opportunity to work in an exciting, multi-disciplinary and multi-cultural environment with senior-level scientists Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Minimum requirements What you’ll bring to the role: • Fields of studies Pharmacometrics or Mathematics/Statistics, Physics, Bioinformatics, Biomedical Sciences or Pharmaceutical Sciences/Pharmacy • Current enrolled in PhD studies • Ideal candidate should have a good familiarity with quantitative methods and longitudinal modeling in one-two domains among the following: mathematical, statistical, biological, pharmacological • Candidates must have excellent oral and written communication skills in English as well as strong problem-solving skills • Working knowledge with software for nonlinear mixed effects modelling, such as Monolix or NONMEM, as well as data exploration tools within R is required • Familiarity with mixed effects modeling is of advantage *The Novartis regulations on hybrid working will apply. Why consider Novartis? 799 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Global Drug Development Business Unit CD&A GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 365178BR Mar 07, 2023 Switzerland Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential unveil therapeutic breakthroughs for patients. Are you a curious, independent scientist eager to work on the development of the next generation of oncology radioligand therapies? The oncology research department at NIBR is recruiting a research scientist with a strong background in cellular and molecular biology to join their Oncology Translational Research group in Basel, Switzerland. The successful candidate will carry out cutting-edge research in the areas of translational/molecular oncology and radioisotope-based therapies in close collaboration with other leading research groups within NIBR. The candidate will be responsible for the generation of high-quality data to support the progress to the clinic of innovative radioligand research programs. By using a variety of molecular and cellular biology approaches the candidate will aim to decipher the cellular mechanisms underlying the activity of radioligand conjugates. Further, the candidate will contribute to the identification of molecular predictors of response and resistance to radioisotope-based therapies, as well as to exploring combination therapy opportunities. The ideal candidate will have a strong background in DNA damage response field and in vitro radiation biology. We seek an experienced, motivated and ambitious scientist wishing to continue a successful scientific career in a fast-paced drug discovery environment. Your responsibilities will include but not be limited to: • Independently design, perform and interpret in vitro experiments under the leadership of the Lab Head • Propose experimental alternatives, explore and introduce novel technologies and approaches • Analyse and effectively report data, as well as presenting the data in different team meetings • Safe and effectively work with radionuclides • Critical reading of the literature and ability to apply it to the project • Closely work with multiple teams across expertise groups within Oncology • Efficiently contribute to maintain a functional laboratory, technical equipment and tools Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring to the role: • MSc or BSc or qualified Lab Technician (apprenticeship/vocational training) in radiobiology, cellular biology, molecular biology or another relevant discipline • At least, 2-5 years of biomedical research. Experience in radiobiology, DNA damage response and/or cell death mechanisms is highly desirable • Proficiency and hands-on experience in applying a wide range of cellular and molecular biological methods (in particular: Immunofluorescence, RNAi, qRT-PCR, cloning, cell culture, cell viability/death assays, transient/stable cell line generation, immunoblotting, ELISA, FACS) • Experience using basic bioinformatics tools to support experimental design, data analysis and interpretation is considered a plus • Excellent presentation and communication skills in English (oral/written) • Used to successfully work within a highly productive and fast-paced environment • Highly collaborative and self-motivated team player, with critical scientific thinking • Excellent organizational skills Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! * This position is eligible for 80-100%* working time, however, some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision NIBR Business Unit Oncology NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 366628BR Mar 07, 2023 Switzerland Job Description 6000! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Are you interested in mitochondrial biology and its role in inflammation? We are seeking a talented and highly motived M.Sc. level scientist in our Biology for Drug Discovery group. Your task will be to support assay optimization and execution for target identification in human immune cells. The project will employ a combination of molecular, cell biology and genetic perturbation (CRISPR) techniques paired with high-throughput read-outs to identify novel therapeutic targets for drug discovery. Interested individuals should be comfortable interacting with a dynamic team as well as contributing individually. Start: June 2023 Duration: 6 months Your responsibilities: • Work in close collaboration with other team members • Applying various cell culture techniques • Running and optimizing high-throughput assays • Applying standard molecular and cell biology techniques (e.g. transfection, FACS, ELISA, cell-line engineering, WB, immunocytochemistry) Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • MSc in a relevant discipline (Biology, Biochemistry, Biomedicine, Biotechnology or similar) • Proficiency in English • Experience/Professional requirement o Good organization and planning skills o Highly motivated and have a sense of urgency & flexibility o Excellent interpersonal & communication skills o Experience in compound, viral-mediated gene transfer or si/shRNA/CRISPR technology advantageous o Experience with high-throughput assay development and/or optimization would be very advantageous Why consider Novartis? 799 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division NIBR Business Unit CBT - NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 358031BR Mar 05, 2023 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With a strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. Early HEOR Associate Directors will work in partnership with Global TAs, other MAP functions, Regions, and priority countries, as well as R&D (NIBR & GDD) to support development and implementation of impactful HEOR and access-relevant evidence generation strategies and tactics that enable better patient outcomes, increased access, enhanced value proposition, and that support new commercial models. They will help to ensure HTA and payer evidence requirements are built into TPPs, clinical development plans, integrated evidence plans, and integrated product strategies. Early HEOR Associate Directors will support development and delivery of all aspects of the HEOR strategy and execution for priority assets from (pre-) POC up to FDP. This role will specifically focus on early assets residing within Global TA teams, up until assets transition to International TA teams. With Global TAs, early HEOR Associate Directors will co-develop HEOR strategies and tactics with specific focus on priority countries (US, CN, DE, JP), major HTA architypes (e.g., UK/CAN) and Budget Impact archetypes (e.g. Italy and/or Spain) needs and feasibility. They will work in close partnership, collaborate and influence strategic TAs cross-functional teams, GPTs, R&D teams in NIBR & GDD, Region and priority Country teams to maximize patient outcomes and access and healthcare system value for early IM assets Your responsibilities include, but are not limited to: • Support the delivery of winning HEOR strategy and tactics, with high quality and on-time availability, including outcomes research and other relevant access and healthcare systems evidence and HEOR deliverables (incl. Global Value Dossier, Cost-effectiveness Models, Budget Impact Models, evidence synthesis, PCO or PRO strategy, access-enabling studies, etc.) • Ensure that payer and healthcare needs are reflected into pivotal clinical programs as well as phase 3b/4, RWE and integrated evidence plans to meet the needs of external experts and institutions involved in reimbursement, pricing, access and healthcare systems decisions. • Help to oversee delivery of access-relevant evidence required by country teams in prioritized markets to achieve reimbursement and other positive funding recommendations and optimal access. • Help to establish and maintain relationships with key economic modelling, outcomes research and HEOR talent and leaders in the field, both outside and inside the company; facilitate sharing of learnings and hands-on utilization of HEOR deliverables and evidence throughout the organization. • Stay abreast of internal and external developments, trends and other dynamics that affect the HEOR and HTA domain and shares learnings with team and the broader organization. • Support Head of Early HEOR, as well as Head of HEOR & PCO in external engagement (with HTA bodies, policy makers, regulatory agencies, HEOR scientific groups) to shape the HTA environment, the HEOR field and informs the organization on opportunities and risks. • Build strong partnerships within Value & Access, Medical Affairs, Global TAs, regional and country counterparts. Collaborate with global regulatory, therapy area policy and access colleagues in seeking early scientific advice from payer, policy maker, and regulatory agencies in prioritized countries. • Embrace change, help implement the new ways of working from Transforming for Growth, develop and improve improved ways of working with a focus on flexibility and efficiency. The role can be based in either Switzerland and/or USA. Our selection process will prioritize associates whose roles may be changing or may be impacted as a result of the Transforming for Growth reorganization. For US based candidates: The ideal location for this role is East Hanover, NJ but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific East Hanover, NJ for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 20% travel. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • 5+ years of experience at pharmaceutical or life-science consulting companies with at least 3 years in HEOR, RWE, market access or other relevant role • Advanced Degree; preferably Ph.D., M.D., MBA, RPh or equivalent • Subject matter expertise in HEOR, incl. deep understanding of HEOR and other approaches to generate payer and HCS evidence; preferably subject matter expertise in RWE, capability in designing winning access-relevant RWE studies, analyzing and publishing RWE data and using the results to make impact with access-relevant customers • Customer-centric mindset, passion, strong knowledge and alignment to payer, patient, access, HCS customers mindset, evidence requirements and decision-making dynamics; deep understanding of payer/HTA evidence requirements and decision-making dynamic cross countries/regions (preferably: an active external network with HEOR, RWE and health policy OLs) • Impact-oriented, enterprise and agile mindset with proven track record of fostering innovation, ability to work in agile manner, and strong process/project management skills • Experience working in global or above-country multidisciplinary drug development and product teams. Preferred: A proven track record of influencing development plans or IEPs to meet the needs of payers or other HCS decision makers; influencing in matrix organization balancing cross-functional perspectives and alignment with business priorities • Preferred: knowledge of research methodology and statistical methods in the field of data analysis, and considerable experience collaborating with quantitative scientists and analysts • Preferred: Significant (3+ years) and recent (post 2015) US in-market experience: includes working in the US market with the local US customers, US health care systems / systems of care, US payors / accounts, US market strategy etc. #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision PHARMA Business Unit GLOBAL PRODUCT & PORTFOLIO STRATEGY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Alternative Location 2 Ireland Alternative Location 3 United Kingdom Functional Area Market Access Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 354316BR Dec 16, 2022 Switzerland Job Description 22! the number of oncology drugs we have on the market and more than 25 new molecular entities in development targeting key molecular pathways in cancer biology. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? As our Clinical Development Medical Director CAR-T, you will be the clinical leader of defined program level activities (e.g. submission activities, briefing books etc.), or a large, complex trial, under the leadership of the (Sr.) GPCH. You may lead a section of a clinical program (e.g., an indication, a new formulation, or a specific development phase). Your responsibilities will include: • Provide clinical leadership and medical strategic input for all clinical deliverables in the assigned project or section of a clinical program if applicable. Clinical deliverables may include clinical sections of individual protocols consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications • Lead development of clinical sections of trial and program level regulatory documents (e.g., Investigator’s Brochures, briefing books, safety updates, submission dossiers, and responses to Health Authorities) • Drive execution of the section of the clinical program in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates if applicable • Coordinate/conduct ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) • May be the Program Manager of other associates (e.g., CSE). Support (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section, may be a core member of the Safety Management Team (SMT), and support overall program safety reporting (e.g., Periodic Safety Update Reports (PSURs), Drug Safety Update Reports (DSURs), and other safety related documents) in collaboration with Patient Safety • Support the Therapeutic Area Head (TAH) by providing medical input into IDP and CTP reviews and contributing/driving development of disease clinical standards for new disease areas. May take on other TA responsibilities as directed by the TAH • As a medical expert, support the (Sr.) GPCH or TAH in interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring boards, advisory boards, patient advocacy groups), internal stakeholders (e.g., CTT, Research, Translational Medicine, Global Medical Affairs, Marketing, HE&OR), and internal decision boards • May work with NIBR (Novartis Institute of Biomedical Research)/Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • MD or equivalent medical degree required. Advanced knowledge and clinical training in a medical/scientific area required (CAR-T), with Medical Board Certification preferred • Fluent oral and written English. • ≥ 5 years of involvement in clinical research or drug development in an academic or industry environment spanning clinical activities in Phases I through IV. ≥ 3 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry • Advanced knowledge of assigned therapeutic area (CAR-T) • Proven ability to establish strong scientific partnership with key stakeholders • Thorough knowledge of GCP, clinical trial design, statistical analysis methodology, and regulatory/ clinical development process • People management experience preferred, this may include management in a matrix environment. Global people management experience desirable • Excellent negotiation, conflict resolution and communication skills (written and oral). Strong interpersonal skills **Some restrictions to flexible working models may apply and will be discussed at interview if applicable Why consider Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit OHD GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358033BR Mar 05, 2023 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With a strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. Launch HEOR Associate Directors will partner across GDD, TAs, MAP, Regions and priority countries to support development and implementation of impactful and winning HEOR, IEP and access-relevant evidence generation strategies and tactics such that enable priority countries to secure broad and rapid access, reimbursement, and adoption for priority pre-launch and launch stage IM brands, enhanced healthcare system value proposition and better patient outcomes, and that support new commercial models. Launch HEOR Associate Directors will support development and delivery of all aspects of the HEOR strategy and execution for priority assets from FDP through launch and post-launch until handover to IBBI. This role will specifically focus on pre-launch and Launch assets residing within International TA teams. With International TAs, early HEOR Associate Directors will co-develop HEOR strategies and tactics with specific focus on priority countries (US, CN, DE, JP), major HTA architypes (e.g., UK/CAN) and Budget Impact archetypes (e.g. Italy and/or Spain) needs and feasibility. They will work in close partnership, collaborate and influence strategic TAs cross-functional teams, GPTs, R&D teams in NIBR & GDD, Region and priority Country teams to maximize patient outcomes and access and healthcare system value for early IM assets. Your responsibilities include, but are not limited to: • Support the development and delivery of winning HEOR strategy and tactics, with high quality and on-time availability, including outcomes research and other relevant access and healthcare systems evidence and HEOR deliverables (incl. Global Value Dossier, Cost-effectiveness Models, Budget Impact Models, evidence synthesis, PCO or PRO strategy, access-enabling studies, etc.) • Help to ensure that payer and healthcare needs are reflected into Phase 3b/4, RWE and integrated evidence plans to meet the needs of external experts and institutions involved in reimbursement, pricing, access and healthcare systems decisions. • Collaborate across divisions and functions to help ensure effective integration of HEOR and payer evidence deliverables (global value dossiers, cost effectiveness and budget impact models) into integrated product strategies, to enable and support in-country reimbursement submissions / negotiations • Partner closely with Regional and Country teams to help design and oversee rollout of global HEOR and payer-evidence strategies and to support local launch preparations and activities concerning access, HEOR, HTA and payer interactions, to achieve reimbursement and other positive funding recommendations and optimal access. • Support interactions with payers and relevant customer groups in priority countries, gathering of Country-level insights and feedback, integration into winning HEOR and payer strategies and tactics, incorporating HEOR perspective in overarching cross-functional product strategies and tactics • Help to establish and maintain relationships with key economic modelling, outcomes research and HEOR talent and leaders in the field, both outside and inside the company; Stay abreast of external developments, trends and other dynamics that affect the HEOR and HTA domain and competitive position of Novartis assets; share learnings and facilitate hands-on utilization of HEOR deliverables throughout the broader organization. • Support Head of Early HEOR, as well as Head of HEOR & PCO in external engagement (with HTA bodies, policy makers, regulatory agencies, HEOR scientific groups) to shape the HTA environment, the HEOR field and informs the organization on opportunities and risks. • Embrace change, help implement the new ways of working from Transforming for Growth, develop and improve improved ways of working with a focus on flexibility and efficiency. The role can be based in either Switzerland and/or USA. Our selection process will prioritize associates whose roles may be changing or may be impacted as a result of the Transforming for Growth reorganization. For US based candidates: The ideal location for this role is East Hanover, NJ but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific East Hanover, NJ for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 20% travel. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • 5+ years of experience at pharmaceutical or life-sciences consulting companies with at least 3 years in HEOR, RWE, market access or other relevant role • Advanced Degree; preferably Ph.D., M.D., MBA, RPh or equivalent • Subject matter expertise in HEOR or RWE, or Market Access or another relevant field • Valued for customer-centric mindset and passion for delivering value to payers / health systems. Understanding of payer/HTA evidence requirements and decision-making dynamic cross countries/regions. Preferably: experience in interacting with HTA external stakeholders and active external network with HEOR, RWE and health policy OLs • Impact-oriented, enterprise and agile mindset with proven track record of fostering innovation, ability to lead in agile organisation, and strong process/project management skills • Highly preferred: operational experience in product launch in priority countries (US, China, Japan, Germany or other Top 10 markets), or at Global or above-country level or HEOR consulting firm • Experience working in global or above-country multidisciplinary product teams. Preferred: a track record in driving implementation of large-scale projects in an agile way; influencing across multiple countries and cross-functional teams; mobilizing, motivating, and coaching country teams in the implementation of global cross-functional launch strategies and tactics • Preferred: knowledge of research methodology and statistical methods in the field of data analysis, and considerable experience collaborating with quantitative scientists and analysts #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision PHARMA Business Unit GLOBAL PRODUCT & PORTFOLIO STRATEGY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Alternative Location 2 Ireland Alternative Location 3 United Kingdom Functional Area Market Access Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 355211BR Oct 26, 2022 Switzerland Job Description 100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have as the Global Head of Study Start-Up! #GCOTransformation The Global Head Study Start-Up (SSU) sets the objectives for the SSU organization in Global Clinical Operations (GCO) including defining and implementing strategy and key priorities, hiring and coaching team leaders, aligning internal and external partners on key tools, processes and metrics to complete the clinical trial portfolio. The role has responsibility for ensuring the Novartis portfolio delivers the fastest start up time in the industry. Responsibilities include but are not limited to: • Driving operational excellence, embedding innovation, and continuous improvement through leadership of agile and adaptive SSU communities of practice comprised of SSU roles and functions from across GCO at the global, hub and country levels. • Developing an empowered organization which can navigate in a matrix environment, deliver consistently improving speed and quality, and pivot in anticipation of data driven business needs. • Building a team culture of expertise, excellence and agility into the SSU trial execution model to optimize impact, deliver on cycle time and process delivery improvements and associate engagement. • Providing proactive leadership through analysis of planned and actual GCO SSU data and industry benchmarking, trends, and regulations to adapt processes, tools and organization as needed to deliver results. • Developing and optimizing SSU resourcing strategy; Hiring, onboarding, development, and retention of SSU Team; responsible for resource allocation of ~40 SSU Leads and CTCEs to support the GCO portfolio including external resource augmentation • Leading Grant Plan strategy and oversight: steer the translation of clinical protocol visit schedule of assessments into intelligent Grant Plan and FMV cost estimations, ensuring clinical, scientific and operational requirements are reflected with accuracy. • Setting standard methodology in establishing country and trial-specific cost benchmarks and budgets to improved efficiency, meet operational and scientific requirements, and positively influence trial operations as it pertains to cost for increasing simplicity and value. Leading effective engagement with FMV and Grant Plan vendor to ensure accuracy and continuous refinement of costs at the assessment level across countries. • Ensure execution and delivery of all global clinical trials across all programs, in accordance with GCP, ICH, SOP’s, and regulations. Have oversight of functional budget and resource allocation and management. Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • 10+ years of pharmaceutical industry experience, with previous experience in either clinical research or project management, in a Pharmaceutical Industry or CROs. Specific SSU experience preferred • At least 6 years experience in people management and/or team leadership • Education (minimum/desirable): University degree in life science, business or operations; Advance degree preferred • Strong clinical and budgeting/finance experience in Pharma research or CRO with excellent understanding of clinical trial development processes and the management of clinical trials • Thorough understanding of the international aspects of drug development process, including extensive knowledge of international standards (GCP/ICH), health authorities (FDA/EMEA), local/National Health Authorities regulations and Novartis standards • Strong leadership and people management skills in global matrixed environment setting and proven track record to develop impactful teams and diverse profiles including manager of manager experience • Proven expert level knowledge of and experience with operational management, and exceptional technical, analytical and quantitative problem solving skills • Credible and confident at building relationships at the leadership level while demonstrating organizational agility. Proven ability to build strong, effective relationships with internal partners. Demonstrated effective influencing and negotiation skills at all levels. • Data and Digital expertise. Experience working with electronic databases, clinical and/or project management planning and reporting and analytics systems. Why consider Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit GDO GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 Ireland Alternative Location 2 United Kingdom Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 360403BR Dec 19, 2022 Switzerland Job Description 2 Billion plus people are affected by diseases of the nervous system having a dramatic impact on patients and families around the world. Neurologic and psychiatric diseases remain as some of the largest challenges in medicine. Novartis is committed to changing the landscape by developing transformative treatments for important neuroscience disorders. The Novartis Institutes for BioMedical Research (NIBR) is the innovation engine of Novartis. We collaborate across scientific and organization boundaries, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs from patients. Within NIBR, Translational Medicine (TM) is the clinical research arm and includes over 900 associates globally. TM plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, and bridging drug discovery and clinical application. Within TM, TM Discovery & Profiling (TMDP) is a group of about 65 physicians and clinical researchers who drive that innovative science from discovery to the patient through the selection, profiling, and effective development of medicines. Translational Medicine Experts (TME’s) oversee Phase 1 and 2 clinical trials to demonstrate proof of concept in patients, creating the case for drugs to proceed to late-stage development and registration. TME’s are also responsible for Phase 3 clinical pharmacology and mechanistic studies. Overall, TM and NIBR deliver about half of the final drug dossier or label information. As the Global Head TM Neuroscience, you will lead a team of TME’s responsible for all early clinical development plans and studies through Proof of Concept, new disease indications, translational research and profiling activities, and clinical pharmacology studies for the Neuroscience Therapeutic Area. You will be a member of the global Translational Medicine Leadership Team, accountable for overall department goals, helping to lead continuous improvement across the department, and enhancing the culture of TM. You will also be a key bridge between NS Research and late phase development and commercial colleagues across the Neuroscience Franchise in Novartis. Your major accountabilities will be to: • Set, communicate and drive strategy for the NS Translational Medicine Therapeutic Area in alignment with the broader organization • Be accountable for setting the biomarker strategy for your group • Prioritize and allocate resources across the team to meet portfolio needs • Co-chair the Disease Area Decision Board with the Research Disease Area Head to decide on targets, compounds, and indications to progress from preclinical ideas to clinical testing • Deliver clear human Proof-of-Concept study outcomes for decisions on new compounds • Collaborate with Development colleagues to agree on Proof-of-Concept criteria and indications and on Development Decision Point criteria • Support Translational Medicine Experts on Development teams after Proof-of-Concept to deliver clinical pharmacology and mechanistic studies • Bring relevant internal and external opinion leaders together to consider the proposed approach to Clinical Proof-of-Concept • Ensure seamless collaboration across Research, Translational Medicine, Development, and other relevant line functions in the development of drug candidates. Work closely and effectively with other TA TM Heads to foster collaborations and lead to cross-DA indication expansion PoC opportunities • Foster strong external clinical collaborations to maintain state of the art clinical approaches • Contribute senior level expertise to Strategic Alliances, Business Development and Licensing due diligence reviews for in licensing and out licensing opportunities • Provide or review Translational Medicine input to meetings and interactions with Health Authorities • Develop talent pipeline through recruitment activities and being a mentor, coach, and educational resource across Novartis responsible for quality of clinical protocols, study reports and submission documents The position can be based in Cambridge, MA USA or Basel, Switzerland. This position will require 25% travel as defined by the business (domestic and/or international). Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring to this role: Education: • MD or MD/PhD, or MD with doctoral thesis in relevant field (Neurology or Neuroscience) Board certification in Neurology or related field. Subspecialty clinical training in Neurodegenerative disorders (preferred) or related subspecialty with appropriate Board Certification(s) Languages: • Fluent English, strong written and oral communication skills Experience: • Leadership position in pharmaceutical/biotech industry or academic medical center combining scientific and medical subspecialty skills, maintaining state-of-the-art clinical approaches and inspiring a culture of continuous improvement, innovation and quality Significant clinical experience with patients with Neurological diseases Direct basic science expertise within Neurological diseases: accomplished independent basic investigator, recognized in your field through peer-reviewed grant funding, publications and congresses Strategic thinker, used to creating major innovations, networking with leading investigators, presenting complex strategic issues in a clear and logical way and driving impactful outcomes Natural ability to manage people, and lead leaders of others; able to provide mentoring at the highest levels including those outside of your own scientific/clinical expertise Used to successfully supporting and impacting experts, scientists and project deliveries across many functions of Research or Development / equivalent Strong program manager: excellent planning, prioritization, problem solving and organizational skills A creative and innovative approach with a sharp and objective intellect Strong cooperative team player, used to being flexible and adapting to a changing environment Resilient, energetic and enthusiastic; responding constructively to challenging new ideas and inputs Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division NIBR Business Unit Translational Medicine Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 356969BR Jan 09, 2023 Switzerland Job Description As an Equipment Specialist you be responsible for assigned manufacturing tasks and activities in keeping with production schedule to ensure that production is maintained to the highest standards of quality and quantity. You will also ensure that manufacturing activities are compliant with GMP, safety and environmental guidelines. Other responsibilities: -Suggest improvement actions (organization, process, safety, hygiene, etc.) at shop floor Documentation Specialist GMP -Prepare, print and consolidate the batch documents, labels... and handover to production operators within the deadlines set according to the production schedule -Follow up on updates and versions of documents in production (procedures and logbooks) -Manage the documents review and approval cycle -Complete the ERP (SAP) and RFT (right first time) databases, make available and participate in the analysis of trends and performance indicators HSE and Quality -Promote and improve the Safety and Quality culture -Ensure overall inspection readiness for area of responsibility Participate in HSE risk assessments KPI and Data Reporting for process teams -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements General HSE Knowledge Knowledge of GMP Manufacturing Process Execution Transportation English/ German language skillsDivision Novartis Technical Operations Business Unit CONTRACT MANUFACTURING Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work Yes Apply to JobAccess Job Account

Job ID 353890BR Feb 27, 2023 Switzerland Job Description Your Responsibilities: Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a di-verse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly The Executive Director, Therapeutic Area (TA) Strategy, will lead a TA (Cardiovascular, Immunology, Haematology, Neuroscience, Solid Tumors or TAx) focused team. She/he will create and update as appropriate a holistic Disease Area (DA) strategy comprising of internal and external licensing / acquisition opportunities for a designated Therapeutic Area (TA) and ensures integrated enterprise alignment across Novartis Institutes for Biomedical Research (NIBR), Global Drug Development (GDD) and Innovative Medicines (IM). In this role, he/she will leverage external benchmarking, analysis and insights, and strong judgement to guide internal choices as part of the holistic Novartis strategy and achieve sustainable growth in short, mid and long-term. The ideal candidate will bring both broad and deep understanding of the pharmaceutical industry, the core TA and its DAs to derive insightful and differentiating competitive advantages over our peers. In addition, she/he will develop and deliver strategic external insights across core TA to support identification of growth opportunities and emerging competitive challenges to growth, and sup-port creation of a third-party view around key strategic levers including commissioning targeted primary research. This role can either be based in Basel, Switzerland and//or Boston, USA. Distant working agree-ments may be offered in these locations based on local employment and/or company guidelines. As a result, please note that international relocation or sponsoring from the US to Switzerland or vice versa will not be offered. Within the US, the ideal location for this role is Boston, MA but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific Boston, MA for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require some travel. Your responsibilities include, but not limited to: Drive Portfolio Strategy and decision making: •Define and drive mid-and-long term portfolio strategy, goals, strategic objectives and leadership aspiration within TA and DAs in collaboration with other functions within S&G, GPSC, IM International, IM US, GDD and NIBR. Orchestrate stakeholder alignment around updates to the strategy as needed, e.g., due to internal or external market events • Identify potential pipeline gaps and make recommendations to address with other S&G functions, IM, GDD and NIBR partners • Collaborate closely with key stakeholders (e.g., GPSC, IM, NIBR, GDD, local functions such as Market Access & Pricing) to facilitate portfolio decision making in the context of our goal of becoming a top 5 Pharma player in the US while maintaining our international leadership • Lead assessments of programs fit to current portfolio strategy and drive content development to facilitate portfolio prioritization / de-prioritization / trade-off discussions for Innovation Management Board (IMB) • Own DA strategic insights development and forecasting, including co-leading Forecasting Consortium challenge sessions for programs prior to IMB review Optimize the early-stage TA portfolio • Serve as NIBR DA commercial lead, providing clear direction on asset portfolio strategic fit, and guiding very early asset shaping, including forecasting, commercial viability, unmet needs (esp. US), evidence strategy and LCM considerations to inform NIBR product strategy. Identify key data requirements to support transition of assets to DDP / FDP (Development Decision Point / Full Development Decision Point) • For assets post DDP / FDP that have transitioned to the GPT, work in collaboration with GPSC lead to optimize sequencing of additional lifecycle indications and develop proposals for IMB review • Support fail-fast approach to ensure timely closure of non-priority assets and resources re-allocation for new priorities Provide external perspective and identify growth opportunities: • Provide commercial input into BD&L, triage opportunities, review non-confidential information and decision making for evaluations and conduct market research together with Insights and Analytics for opportunity sizing and business case preparation. Drive strategic insights and outside-in challenge of internal assumptions around core pipeline and external opportunities (e.g., forecast assumptions) and within key portfolio governance processes. Drive white space exploration with Novartis Strategy and diligence and external landscape mapping with BD&L and M&A • Lead commercial discussions on partnering opportunities for internal and external portfolio with top Pharma companies. Leads, in partnership with IM, the commercial DD activities and synthesize commercial recommendations. Leads, in partnership with IM, Licensing and Merger and Acquisition commercial evaluations • Assist Group Investor Relations and the CEO Office with dissemination of key strategic insights Others: • Provide leadership support to TA Strategy Directors in developing value proposition and recommendations for key milestones (e.g., DDP, FDP) on projects in the TA • Coach and develop more junior talents within the group Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Advanced degree (PhD, MD, or other advanced University degree) or equivalent experience in life science/healthcare; MBA, consulting, or equivalent experience highly desirable • In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) • Highly agile having the capacity to manage several strategic DAs within a TA and multiple programs internal and external • Substantial experience evaluating new product opportunities through M&A, BD&L, and internal re-search programs • At least 10-12 years of pharma industry and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, and analyzing primary research • Experience of strategy development and asset shaping early in lifecycle (any functional perspective) • Recent (post 2015) local US experience preferred; local US experience includes working within the US market with the local US customers, US health care systems / systems of care, US payors / accounts, etc. and driving US market strategy • Recent (post 2015) experience in global role preferred • A track record of successfully working with Commercial, Medical Affairs, Market Access, as well as Business Development & Licensing • Ability to comfortably engage with senior leadership as well as mid-career associates to influence and challenge with excellent interpersonal skills • Strong financial modeling and assessments for valuation skills and experience in strategic and competitive data analysis and insights generation, leveraging digital tools • Strong strategic vision and excellent communication, consensus building and influencing skills • Enterprise maximization mindset in balance with TA needs: able to align to broader enterprise strategy for trade-off against shorter-term payoffs to avoid unnecessary investments. Desire to make bold choices to stop/ divest / reduce investment • Strategic collaboration and cross functional leadership; effectively work in matrix balancing cross-functional perspectives and alignment with business priorities against flexible resourcing #transformingforgrwth Why Novartis? 766 million. That’s how many lives our products touched in 2021 and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis Imagine what you could do at Novartis! Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network We are Novartis. Join us and help us reimagine medicine.Division CORPORATE Business Unit Group Corporate Affairs & Global Health Location Switzerland Site Basel Company / Legal Entity Novartis International AG Alternative Location 1 USA Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 353891BR Feb 27, 2023 Switzerland Job Description Your Responsibilities: Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly The Director, Therapeutic Area (TA) Strategy, will support a TA (Cardiovascular, Immunology, Haematology, Neuroscience, Solid Tumors or TAx) focused team. She/he will support the creation and update of a holistic Disease Area (DA) strategy comprising of internal and external licensing / acquisitions opportunities for a designated TA and supports integrated enterprise alignment across Novartis Institutes for Biomedical Research (NIBR), Global Drug Development (GDD) and Innovative Medicines (IM). In this role, he/she will leverage external benchmarking, analysis, insights, and judgement to support the TA Strategy Head in developing a holistic Novartis strategy that achieves sustainable growth in short, mid and long-term. The ideal candidate will bring understanding of the pharmaceutical industry, the core TA and its DAs to derive insightful and differentiating competitive advantages over our peers. In addition, she/he will support development and delivery of strategic external insights across the core TA to inform identification of growth opportunities and emerging competitive challenges to growth, and support creation of a third-party view around key strategic levers, including commissioning targeted primary research. This role can either be based in Basel, Switzerland and//or Boston, USA. Distant working agree-ments may be offered in these locations based on local employment and/or company guidelines. As a result, please note that international relocation or sponsoring from the US to Switzerland or vice versa will not be offered. Within the US, the ideal location for this role is Boston, MA but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide reloca-tion as a result. If associate is remote, all home office expenses and any travel/lodging to specific Boston, MA for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require some travel. Your responsibilities include, but are not limited to: Drive Portfolio Strategy and decision making: • Support definition and delivery of mid-and-long term portfolio strategy, goals, strategic objectives and leadership aspiration within TA and DAs in collaboration with other functions within S&G and in IM, GSPC, GDD, & NIBR. Help drive stakeholder alignment around updates to the strategy as needed, e.g., due to internal or external market events • Identify potential pipeline gaps and make recommendations to address with other S&G functions, IM, GDD and NIBR partners • Collaborate closely with key stakeholders (e.g., GPSC, IM, NIBR, GDD, local functions such as Market Access & Pricing) to facilitate portfolio decision making in the context of our goal of becoming a top 5 Pharma player in the US while maintaining our international leadership • Support assessments of programs fit to current portfolio strategy, and drive content development to facilitate portfolio prioritization / de-prioritization / trade-off discussions for Innovation Management Board (IMB) • Support DA strategic insights development and forecasting, including Forecasting Consortium challenge sessions for programs prior to IMB review Optimize the early-stage TA portfolio • Support forecasting, commercial viability, unmet needs (esp. US), evidence strategy and LCM considerations to inform NIBR product strategy, including identification of key data requirements to support transition of assets to DDP / FDP (Development Decision Point / Full Development Decision Point) • For assets post DDP/ FDP that have transitioned to the GPT, work in collaboration with GPSC lead to optimize sequencing of additional lifecycle indications and develop proposals for IMB review Provide external perspective and identify growth opportunities: • Provide commercial input into BD&L, triage opportunities, review non-confidential information and decision making for evaluations and conduct market research together with Insights and Analytics for opportunity sizing and business case preparation. Drive strategic insights and outside-in challenge of internal assumptions around core pipeline and external opportunities (e.g., forecast assumptions) and within key portfolio governance processes. Support white space exploration with Novartis Strategy and diligence and external landscape mapping with BD&L and M&A •Support commercial discussions on partnering opportunities for internal and external portfolio with top Pharma companies, support commercial DD activities and synthesis of commercial recommendations. Support Licensing and Merger and Acquisition commercial evaluations • Assist Group Investor Relations and the CEO Office with dissemination of key strategic insights Others: • Provide support to the broader TA Strategy Group in helping challenge and develop other TA Strategy Directors Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Advanced degree (PhD, MD, or other advanced University degree) or equivalent experience in life science/healthcare; MBA, consulting, or equivalent experience highly desirable • In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) • Highly agile having the capacity to support several strategic DAs within a TA and multiple programs internal and external • Substantial experience evaluating new product opportunities through M&A, BD&L, and internal re-search programs • At least 5-7 years of pharma industry and/or medical device experience in Research & Development and/or commercial functions with experience conducting, commissioning, and analyzing primary re-search • Experience of strategy development and asset shaping early in lifecycle (any functional perspective) • Recent (post 2015) local US experience preferred; local US experience includes working within the US market with the local US customers, US health care systems / systems of care, US payors / ac-counts, etc. and driving US market strategy • A track record of supporting areas such as Commercial, Medical Affairs, Market Access, as well as Business Development & Licensing • Ability to comfortably engage with senior leadership to influence and challenge with excellent inter-personal skills • Strong financial modeling and assessments for valuation skills and experience in strategic and competitive data analysis and insights generation, leveraging digital tools • Strong communication, consensus building, and influencing skills • Enterprise maximization mindset in balance with TA needs: able to align to broader enterprise strategy for trade-off against shorter-term payoffs to avoid unnecessary investments. Desire to make bold choices to stop/ divest/ reduce investment Strategic collaboration and cross functional leadership; effectively work in matrix balancing cross-functional perspectives and alignment with business priorities against flexible resourcing #transformingforgrowth Why Novartis? 766 million. That’s how many lives our products touched in 2021 and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis Imagine what you could do at Novartis! Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] let us know the nature of your request and your contact information. Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network We are Novartis. Join us and help us reimagine medicine.Division CORPORATE Business Unit Group Corporate Affairs & Global Health Location Switzerland Site Basel Company / Legal Entity Novartis International AG Alternative Location 1 USA Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 356629BR Nov 21, 2022 Switzerland Job Description Reporting to the CEO, the CEO office team drive high profile, company-wide strategic initiatives that address the top priorities for the company whilst supporting the five core pillars of our Strategy. While our roles are highly visible and demanding, we have a unique opportunity to shape global healthcare trends and work with senior leaders across our businesses to execute our company’s agenda. Key Responsibilities: • Independently drives strategic business projects for Sandoz, the CEO and the Exec-utive Committee • Generates strategic insights based on best-in-class analysis, distils outputs and rec-ommendations which enable informed decisions of top-level leaders • Actively contribute to annual strategic planning process • Invests in knowledge / functional spike on behalf of strategy team • Proactively identifies trends and opportunities to shape the CEO and SEC agenda • Provide insight into Health Care Systems as our core customer • Develop network of functional experts and strategy managers across Sandoz • Work with the rest of the office of the CEO to ensure that the CEO is fully supported when it comes to his activities and responsibilities, and to ensure that the organization is aligned on key priorities and executing towards those Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Advanced degree such as MD, PhD or MBA desired • High Proficiency in English • Deep knowledge of the Pharmaceutical Industry. Experience in the Generics industry will be considered as a significant plus • Minimum of 5 years’ experience in the pharmaceutical/ healthcare industry (preferably in generics). Experience at a top consulting firm or significant other experience such as industry will be considered as a plus. • Track record of business impact • Advanced analytical skills (problem structuring and problem solving), able to understand/ interpret complex analyses • Excellent in cross-functional collaborations and project management • Excellent communications skills and ability to interact with senior stakeholders • Excellent IT skills, particularly MS Power Point and MS Excel • Passionate, positive attitude, outstanding flexibility, adaptability and sense of accountabilityDivision SANDOZ Business Unit SANDOZ BUSINESS OFFICE Location Switzerland Site Basel Company / Legal Entity Sandoz AG Alternative Location 1 Germany Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 366490BR Mar 06, 2023 Switzerland Job Description Your desire is to start a career in an international company? You are interested in business administration topics and you are comfortable to talk and study in English as well as exchanging with fellow students from abroad? This is your chance to apply for our cooperative study program in BWL- International Business (held in English) together with the Duale Hochschule Baden-Württemberg! Duration: 01.10.2023 – 30.09.2026 This is our offer: • Insights into different departments within a multinational company, like e.g. Human Resources, Marketing, Finance or language specific areas like communications • Transfer of knowledge into practical experience in our departments during the practical phases (3 months rhythm) • Studies at the DHBW (Dualen Hochschule Baden-Württemberg) in Lörrach, mainly consistent of BWL (business administration) classes like controlling, human resources, law and general economic topics but also with a strong focus on intercultural competency and detailed analysis of different markets • Graduation after 3 years (6 semesters) in Bachelor of Arts – BWL-International Business • Salary will be paid during the whole duration of study Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • General University Entrance Qualification (with additional successful DELTA-Examination from DHBW), Abitur or Matura • High willingness to perform • High degree of independency and flexibility • Good team player • Very good knowledge in English and German Why Novartis? 236 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division CTS Business Unit HR NBS Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 366492BR Mar 06, 2023 Switzerland Job Description You are interested in the wellbeing of employees? You like the interaction with people and submit your innovative ideas for a better work environment and digitalization? You are looking for a training program which combines theoretical knowledge with practical experience? This is your chance to apply for our cooperative study program in BWL- Human Resources Management together with the Duale Hochschule Baden-Württemberg! Duration: 01.10.2023 – 30.09.2026 This is our offer: • Insights into different Human Resources areas within a multinational company, like e.g. Early Talents, Compensation & Benefits • Transfer of knowledge into practical experience in our departments during the practical phases (3 months rhythm) • Studies at the DHBW (Dualen Hochschule Baden-Württemberg) in Lörrach, mainly consistent of BWL (business administration) classes like controlling, law and general economic topics but also with a strong focus on human resources topics like digital transformation • Graduation after 3 years (6 semesters) in Bachelor of Arts – BWL-Human Resources Management • Salary will be paid during the whole duration of study Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • General University Entrance Qualification (with additional successful DELTA-Examination from DHBW), Abitur or Matura • High willingness to perform • High degree of independency and flexibility • Good team worker • Very good knowledge in English and German Why Novartis? 236 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division CTS Business Unit HR NBS Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 367910BR Mar 17, 2023 Switzerland Job Description 46’000! That’s the number of patients in clinical trials at Novartis. Our vision in GDD is to engage these patients, making sure we have the right patients, in the right trials, at the right sites, at the right time. Do you want to use your expertise to help us reimagine medicine? Then we would like to hear from you for current and future opportunities within our development units for: • Oncology • Neuroscience & Gene Therapy • Global Health • Cardiovascular, Renal & Metabolism • DUx • Immunology After your Master’s, Doctoral or Post-doctoral qualification, do you want to learn more about and gain more experience in Clinical Development at a leading global healthcare company and see how drugs are developed to help addressing unmet needs and reimagining medicine? Do you have a collaborative mindset and take ownership of assigned tasks, and are you able to quickly adapt to different multicultural teams and diverse concepts? Besides that, do you have excellent problem-solving skills? The Clinical Development Postgraduate Training Program is an opportunity to discover the science of Clinical Development. Duration and start of training: 2 years with an expected start date in September 2023 Your responsibilities include, but are not limited to: • Acquiring an understanding of the organization, how Clinical Functions and Clinical Development Units work together to develop solutions that address unmet needs for patients and discover the science of clinical development • Contributing to development of trial-related documents (e.g., Clinical Trial Protocols (CTPs), informed consent form, case report forms, data analysis plan, data monitoring committee charters, reports, publications) for assigned clinical trial(s) consistent with the Clinical Development Plan. May include developing materials for trial-related advisory boards, data monitoring committees, investigators meetings, and protocol training meetings for Novartis local & global medical organizations • Conducting ongoing medical, clinical, and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from the Medical Lead • Managing & preparing patient safety reports on trial data for use of safety and clinical boards (e.g., Safety Management Team, Global Clinical Team, Global Program Team) with appropriate oversight from the Medical Lead • Providing input into final analyses and interpretation including the development of the Clinical Study Report(s), publications, and internal/external presentations #LI-Hybrid Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Advanced degree in life-sciences is required, such as: Master Degree in one of the (bio) sciences, MPh, PhD, PharmD (completed within the last 2 years) • Clinical development training/class module at university/institution, knowledge of GCP, clinical trial design, statistics, and regulatory or clinical development exposure preferred • Seeking new and different experiences for learning in the pharmaceutical industry and curiosity about clinical development • Strong interpersonal skills i.e. can demonstrate your ability to communicate well and establish effective working relationships with people from a variety of backgrounds/cultures and at different hierarchical levels inside and outside the company Why Novartis? 743 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Global Drug Development Business Unit GLOBAL HEALTH DU GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 366302BR Mar 03, 2023 Switzerland Job Description 250! The number of genomics research projects that are waiting for your data analysis expertise every year. Your work will be important towards faster discovery and development of next generation breakthrough therapies for unmet medical need. The Immunology Disease Area at the Novartis Institutes for BioMedical Research (NIBR) in Basel is seeking a highly motivated postgraduate to join our Data Science team for an internship. Our team provides translational data science expertise and support to clinical and preclinical drug discovery programs targeting autoimmune diseases and chronic inflammation. We integrate and analyse internal and public biomedical data to enable strategies for patient stratification, compound differentiation, biomarker discovery, target identification and disease understanding. Timing: as soon as possible Duration: 6 month Your responsibilities:  Analyse and integrate multiple single-cell transcriptomics (scRNA-seq) datasets to identify pathways, signatures, and biomarkers which impact autoimmune diseases  Benchmark and validate computational methods and bioinformatics pipelines  Apply statistical and machine learning methods to characterize disease phenotypes and drug treatment effects  Contextualize and interpret statistical results to formulate hypothesis on mechanisms of disease  Visualize and present results of your work to an interdisciplinary audience Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role:  Master’s degree in bioinformatics, computational biology, or a related field  Excellent skills in data analysis, data visualization and statistical programming in R/Bioconductor  Good knowledge of computational, statistical methods for handling high dimensional ‘omics’ datasets. Prior experience in analysing scRNA-seq data is highly desirable  Good understanding of biology and ability to contextualize results  Ability to work independently and as part of an interdisciplinary team  Excellent communication skills and knowledge of English. Why consider Novartis? 799 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division NIBR Business Unit IMMUNOLOGY - NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 357616BR Mar 08, 2023 Switzerland Job Description 100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have as the Head of Vendor Program Leads! #GCO In this role you will ensure the development of a program level vendor strategy for the execution and delivery of all global clinical trials across all programs, in accordance with established category strategies. You'll be accountable for the successful execution of strategies to support portfolio deliverables and have complete oversight of budget and resource allocation including enterprise review of VPL resources. You'll provide mentorship to your Program Leads and drive operational excellence through process improvement and knowledge sharing across the function. We want you to develop an empowered organization which can navigate in a matrix environment and adjust quickly to business needs. Responsibilities include but are not limited to: • Lead an organization of 10+ Vendor Program Leads across global locations • Drive efficient allocation and resourcing to Global Clinical Operations (GCO) and Vendor Partnerships & Governance (VPG) priorities. • Establish objectives for VPL organization in alignment with GCO and VPG organization priorities. • Build the best talent and an empowered culture to foster high performance in a matrix environment. • Sponsor key talents across the organization to ensure business critical roles and talent continuity. • Hiring, onboarding, development, and retention of VPLs and serve as the single point of contact for internal/external customers. • Utilize data and insights to monitor overall performance of VPL and be responsible for providing quarterly business review updates on status program strategies, risks and issues from a portfolio view. • Sponsor key initiatives to improve operational efficiency within the Vendor Program Lead organization as well as the broader VPG organization Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • We are looking for an industry leader with significant experience and expertise in drug development processes, knowledge of strategic partnership management, and related vendor oversight processes and activities. This will include but is not limited to Regulatory, Trial Management, and relevant development units. • Education (minimum/desirable): Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred (PhD/MD/ PharmD/ Masters) • 10 or more years of experience in pharmaceutical clinical drug development. • Experience in managing associates globally and in management in a matrix organization. • Proven ability to lead cross functional matrix teams • Strong leadership, interpersonal and problem-solving skills. High resilience and ability to advocate and implement new ways of working. • Extensive knowledge of Vendor landscape and vendor service offering how this translates to the clinical development process. • Strong organizational understanding and customer management skills. • Strong relationship-building skills; can influence, negotiate with and motivate executive leadership Why consider Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit GDO GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 United Kingdom Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 362973BR Feb 03, 2023 Switzerland Job Description 1 out of 10 people are suffering from immunological diseases. The Immunology Disease Area at the Novartis Institutes for Biomedical Research (NIBR) is investing in the discovery of novel and transformative therapies to improve the life of affected patients. As part of this effort, we are seeking an innovative and highly motivated Principal Scientist or Senior Principal Scientist to guide discovery approaches in the field of complement with a focus on small molecule drugs. Your responsibilities will include but not be restricted to: You will be responsible for leading a state-of-the-art laboratory of BSc/MSc level scientists to discover and develop small molecule complement inhibitors for a number of autoimmune and inflammatory diseases. This will include the use of enzymatic, biophysical, biochemical, and cellular assays to identify and characterize novel inhibitors and to discover appropriate biomarkers for monitoring complement activation in various tissues. • Contribute to and/or lead early drug discovery projects within multidisciplinary teams up to clinical proof-of-concept studies in patients • Define and execute on innovative scientific strategies, test novel disease-relevant hypotheses and develop transformative therapies • Closely collaborate with scientists, clinicians, and technology experts across different departments in the global organization. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring to the role: • A PhD degree with a minimum of 2-3 years of postdoctoral experience in biochemistry, protein science and immunology • Significant scientific accomplishments and successful collaborations documented by publications in high-impact journals • Strong technical and theoretical background/expertise in complement biology, innate immunity, and translational research • Proven track record of leadership, strategic thinking, creativity, and risk taking • Excellent organization, communication, presentation and analytical skills Desirable requirements: • Experience as an independent research scientist in an academic setting and/or in the pharmaceutical/biotech sector • Proven success in independently initiating and leading interdisciplinary research projects Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! * This position is eligible for 80-100%* working time, however, some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision NIBR Business Unit AUTO/TRANS/INFL - NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 367775BR Mar 16, 2023 Switzerland Job Description 10! That’s how many pipeline projects Immunology has in Phase 3 or registration and over 25 projects in Phase 1/2. Immunology is a key area for Novartis, and one where we have a long tradition. From the launch of Sandimmune (cyclosporin) 30 years ago to enable solid organ transplantation, to the current blockbusters Ilaris (anti-IL-1) and Cosentyx (anti-IL-17), Novartis has long had a focus on treating immunological diseases in rheumatology, dermatology, organ transplant, and autoimmune diseases. And we’re not looking back! The Novartis Institutes for BioMedical Research (NIBR) is the innovation engine of Novartis. We collaborate across scientific and organization boundaries, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs from patients. Within NIBR, Translational Medicine (TM) is the clinical research arm and includes over 900 associates globally. TM plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, and bridging drug discovery and clinical application. Within TM, TM Discovery & Profiling (TMDP) is a group of about 65 physicians and clinical researchers who drive that innovative science from discovery to the patient through the selection, profiling, and effective development of medicines. Translational Medicine Experts (TME’s) oversee Phase 1 and 2 clinical trials to demonstrate proof of concept in patients, creating the case for drugs to proceed to late-stage development and registration. TME’s are also responsible for Phase 3 clinical pharmacology and mechanistic studies. Overall, TM and NIBR deliver about half of the final drug dossier or label information. As the Global Head TM Immunology, you will lead a team of TME’s responsible for all early clinical development plans and studies through Proof of Concept, new disease indications, translational research and profiling activities, and clinical pharmacology studies for the Immunology Therapeutic Area. You will be a member of the global Translational Medicine Leadership Team, accountable for overall department goals, helping to lead continuous improvement across the department, and enhancing the culture of TM. You will also be a key bridge between Immunology Research and late phase development and commercial colleagues across the Immunology Franchise in Novartis. Your major accountabilities will be to: • Set, communicate and drive strategy for the Immunology Translational Medicine Therapeutic Area in alignment with the broader organization • Be accountable for setting the biomarker strategy for your group • Prioritize and allocate resources across the team to meet portfolio needs • Co-chair the Disease Area Decision Board with the Research Disease Area Head to decide on targets, compounds, and indications to progress from preclinical ideas to clinical testing • Deliver clear human Proof-of-Concept study outcomes for decisions on new compounds • Collaborate with Development colleagues to agree on Proof-of-Concept criteria and indications and on Development Decision Point criteria • Support Translational Medicine Experts on Development teams after Proof-of-Concept to deliver clinical pharmacology and mechanistic studies • Bring relevant internal and external opinion leaders together to consider the proposed approach to Clinical Proof-of-Concept • Ensure seamless collaboration across Research, Translational Medicine, Development, and other relevant line functions in the development of drug candidates. Work closely and effectively with other TA TM Heads to foster collaborations and lead to cross-DA indication expansion PoC opportunities • Foster strong external clinical collaborations to maintain state of the art clinical approaches • Contribute senior level expertise to Strategic Alliances, Business Development and Licensing due diligence reviews for in licensing and out licensing opportunities • Provide or review Translational Medicine input to meetings and interactions with Health Authorities • Develop talent pipeline through recruitment activities and being a mentor, coach, and educational resource across Novartis responsible for quality of clinical protocols, study reports and submission documents The position is based in Basel, Switzerland and will require 25% travel as defined by the business (domestic and/or international). We support international family relocation and integration support to Switzerland. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring to this role: Education: • MD or MD/PhD, or MD with doctoral thesis in relevant field (Rheumatology, Allergy & Immunology, Transplantation, or related field) Board certification in a relevant field. Subspecialty clinical training in Immunology disorders (preferred) or related subspecialty with appropriate Board Certification(s) Languages: • Fluent English, strong written and oral communication skills Experience: • Leadership position in pharmaceutical/biotech industry or academic medical center combining scientific and medical subspecialty skills, maintaining state-of-the-art clinical approaches and inspiring a culture of continuous improvement, innovation and quality • Significant clinical experience with patients with Immunology diseases • Direct basic science expertise within Immunological diseases: accomplished independent basic investigator, recognized in your field through peer-reviewed grant funding, publications and congresses • Strategic thinker, used to creating major innovations, networking with leading investigators, presenting complex strategic issues in a clear and logical way and driving impactful outcomes • Natural ability to manage people, and lead leaders of others; able to provide mentoring at the highest levels including those outside of your own scientific/clinical expertise • Used to successfully supporting and impacting experts, scientists and project deliveries across many functions of Research or Development / equivalent • Strong program manager: excellent planning, prioritization, problem solving and organizational skills • A creative and innovative approach with a sharp and objective intellect • Strong cooperative team player, used to being flexible and adapting to a changing environment • Resilient, energetic and enthusiastic; responding constructively to challenging new ideas and inputs Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division NIBR Business Unit Translational Medicine Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 366247BR Mar 02, 2023 Switzerland Job Description 20 years of untapped data waiting for the right person to find the next breakthrough in innovative medicines. This Postgraduate role will support our innovation pipeline in the NIBR Biologics Center (NBC) contributing to the development of best-in-class manufacturing cell lines for the production of Biologics e.g. multispecific proteins. Your responsibilities include, but are not limited to: • Generate stable, transgenic producer cell lines including CHO • Perform state-of-the-art cell line engineering activities • Design and molecular cloning of DNA vectors and genetic elements • Perform characterization experiments on engineered cells including upstream production processes and genetic characterization on DNA and RNA samples • Document experiments using electronic lab book and according to line function requirements • Analyze and collect experimental data & present scientific interpretation in internal meetings Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Recent Master graduate with a Degree in Biotechnology, Biology or Biochemistry • Strong experience in mammalian (suspension) cell culture • Experience in DNA vector design & cloning and cell & genome engineering • Good experience and understanding of molecular biological methods • Proficient in English (written and spoken) Desirable requirements: • Experience in microscopy and flow cytometry • Knowledge in NGS • Knowledge of data analysis software Please submit a cover letter that includes your motivation for the position and from when you will be available. Thank you. Start date: 15th June 2023 Duration: 6 months Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. And while we’re proud of that, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are empowered to ask new questions, make bolder decisions and take smarter risks. We are Novartis. Join us and help reimagine medicine.Division NIBR Business Unit BIOLOGICS NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 365205BR Mar 02, 2023 Switzerland Job Description Supports the Solution Owner by translating the business requirements to technical solutions and required implementations. Also defines required technical enablers to keep the solutions in good health Major Accountabilities •Actively contribute to professional and reliable technology delivery for business systems, platforms, and processes for business domain/function(s) in scope. •Accountable to plan, define, and develop high-level designs for solutions •Working with Enterprise Architects to align solution architecture with enterprise architecture standards •Actively contribute to on time, within budget, compliant, secure, and quality delivery of portfolio/ respective engagements. •Effectively engage with the chosen SI Partner(s) and collaboratively strive to deliver business value. •Contribute enterprise grade and state of the art Solution Design & Architecture with maximizing re-usability, configurability and scalability. •Ensure top class and state of the art engineering delivery, code management, automation and strive for highest efficiency. •Supporting Project Managers in developing solution roadmaps, incl. evaluating change & run decisions •Ensure the overall user experience is taken into account when designing deploying new solutions and services. •Ensure adherence to Security & Compliance policies and procedures as well as with other Sandoz guidelines and standards. •Working with Supplier Management to evaluate options for solutions and services ensuring external requirements and features are incorporated into solution designs Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Education •Master of Science degree in information technology, software engineering, computer science or related field •Certification in and/or experience with Agile/DevOps methodologies is a plus •Certification or accreditation in enterprise architecture, The Open Group Architecture Foundation (TOGAF), or related certification is a plus Experience •Proven experience in engineering and software architecture design. •Experience in product delivery and architecture, including as an Architect of enterprise solutions •Experience with change management through process engineering and/or participating in large-scale IT change / transformation programs •Experienced in guiding and developing teams across wide geographies & in collaborating with business and technical stakeholders to align a strategic IT service portfolio with business needs. •Excellent written, oral communication and presentation skills to present features and solution recommendations to senior stakeholders. •ServiceNow, Document management systems, DevOps, ITIL ProcessesDivision SANDOZ Business Unit Global ERC SZ Location Switzerland Site Basel Company / Legal Entity Sandoz AG Alternative Location 1 Czech Republic Functional Area Technology Transformation Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 350062BR Mar 14, 2023 Switzerland Job Description 500! The number of regulatory documents we authored last year. As an Expert Regulatory Writer you will develop documents which cover all Novartis therapeutic areas and therapies, ranging from Phase I to IV Clinical Study Reports to regulatory submission documents (e.g. Clinical Summaries, Clinical Overview, Briefing Books, answers to Health Authority Questions) for New Drug Applications (NDA), supplemental NDAs, Marketing Authorization Applications and Type II variations. Your responsibilities include, but are not limited to: • To author, review and lead high quality clinical and safety documents: complex Clinical Study Reports (CSR), Risk Management Plans (RMP), complex Common Technical Document (CTD) submission documents (clinical overviews, summaries of clinical efficacy and safety, summaries of clinical pharmacology and biopharmaceutics), other documents for health authorities (e.g., Briefing Books, answers to questions). • Lead writing team for complex submissions, actively contributing to key messaging and pooling strategy, providing expert content guidance for clinical portions of the CTD, and ensuring compliance of documentation to internal company standards and external regulatory guidelines. • Ad-hoc member of Clinical Trial Team and extended member of Safety Management Team. Core member of multiple Clinical Submission Teams (CST). Extended member of Global Clinical Teams (GCT). • Input into planning of data analyses and presentation (statistical analysis plan review and meetings) used in CSRs, submission documents and/or answers to questions. • Documentation expert in GCTs and CSTs to ensure compliance to internal company standards and external regulatory guidelines. Provide content and strategic expertise for clinical portions of the CTD. Maintain audit, SOP and training compliance. • Program Writer for large and/or complex programs ensuring adequate medical writing resources are available for assigned program and consistency between documents. • Lead process improvement in Regulatory Writing and Submissions (RWS) and cross-functional initiatives and/or activities. • Can identify training needs to develop high level of performance within RWS. Coach and/or mentor less experienced writers & lead in cross-functional communication to optimize feedback and input towards high quality documents. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Minimum Life Science degree or equivalent is required. Advanced degree or equivalent education/degree in life sciences/healthcare is desirable. • 6 + years regulatory writer and or medical writer experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus experienced knowledge of medical writing processes. • Expert knowledge of and repeat experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements). • Expert knowledge, extensive experience, and demonstrated record of accomplishment in global registering of drugs. • Expert knowledge of biostatistics principles. • Excellent communication skills (written, verbal, presentations). Fluency in English is essential. • Shown ability to prioritize and lead multiple demands and projects. • Experience in leading global, cross-functional teams or complex global projects. • Demonstrated ability to motivate and coach people. WHY NOVARTIS? 743 million lives were touched by Novartis medicines in 2021 with 21 major drug approvals (US, EU, Japan, China), and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Global Drug Development Business Unit GDO GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 361257BR Feb 01, 2023 Switzerland Job Description 700! That’s the number of talented chemists within Global Discovery Chemistry (GDC) at the Novartis Institutes for BioMedical Research (NIBR) who design and make new molecules for treating patients. At Novartis we are reimagining medicine to improve and extend people's lives. We use innovative science and technology to address some of society's most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. How can we continue to advance our science to help patients in need? We believe the answers are found when curious, courageous, and collaborative people are empowered to ask new questions, make bolder decisions, and take smarter risks. In Global Discovery Chemistry (GDC) at the Novartis Institutes for BioMedical Research (NIBR) in Basel, Switzerland, we are at the core of Novartis’ purpose. We are looking for a highly motivated, passionate researcher with a strong scientific background in radiochemistry or related disciplines, a curious mind-set, and cultural agility to work in a highly dynamic team to identify new targeting vectors for radioligand therapies (RLT). Join us and help reimagine medicine! Your responsibilities will include, but are not limited to: • You will independently plan and execute the synthesis of radioligands (peptides and/or proteins) labelled with various radiometals, as part of a dynamic team of associates according to a program defined by the project team. • You will propose, evaluate, interpret and validate new radiolabeling procedures with radiometals including the use of automation and advanced formulation development. • You will collect and perform the quality control of radioligands by High Performance Liquid Chromatography (HPLC), Thin Layer Chromatography (TLC) and Size Exclusion Chromatography (SEC) in the radiochemistry lab environment and release the radioligands for preclinical studies. • You will be responsible for following implemented radiation safety regulations (e.g. trainings, dosimetry, release and disposal of radioactive waste). • You will evaluate novel technologies including possibilities for automation to increase daily work efficiency. • You will collaboratively work in a multidisciplinary project team to characterize novel radioligand therapies in the upsurging oncology disease area. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring to the role: • A passion for hands-on chemistry experimentation in the laboratory with the ability to critically interpret results, build new experimental hypotheses, and take smart decisions. • A bachelor or apprenticeship in chemistry, pharmacy, or related discipline with strong interest and willingness to learn radiochemistry and radiolabeling techniques. We also encourage applicants from an Organic Chemistry or a Nuclear Physics background. • Minimum of 3 years practical experience in chemistry experimentation in the laboratory and profound knowledge of standard IT applications (e.g. E-Notebook, ChemDraw, software controlled lab equipment). • Previous experience with radiochemistry/radiolabeling is an asset. • A mind-set of curiosity, creativity, collaboration and openness to diverse thinking, with an enthusiasm to develop yourself also beyond your current comfort zones. • An organized working style, eye for detail, flexibility and commitment to high quality. • A desire to collaborate with a highly dynamic team, discuss science and contribute to the next generation of RLTs. • Good oral and written communication in English and/or German; applications in German are welcome too. 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! * Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision NIBR Business Unit Global Discovery Chemistry Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 367284BR Mar 13, 2023 Switzerland Job Description no 1 ! reason to join BDSS as a QC Analyst....because in the Biopharmaceutical network we operate as the ‘Launching Machine’ for Novartis Biologics; working to bring our lifechanging medicines from clinical trial stage to market in record time. We are helped do this by facilities and infrastructure that are top class, but also by an environment that is open-minded, and one which supports people to develop with mentoring, training and the opportunity to experience different disciplines. What you will do: • Sample storage and management • Perform and document lab analysis (standard and more complex techniques) • Ensure all activities in compliance with cGxP, incl. data integrity • Support analytical investigations and OOx • Implementation of innovative DP/DS methods from development • Participation in co-validation activities or analytical transfers • Support method development and validation • Support troubleshooting • Responsible for GMP Instruments • Data Integrity check • Comply with all HSE guidelines Pls note we are offering a Novartis contract here of 1 year duration. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring? • Professional experience ca. 3-5 years in GMP environment and analytics (e.g., Quality Control) • Fluent German both written & spoken. 743 million! the total no of patients we reached in 2022 through our collective efforts to reimagine medicine and make a real difference to the lives of patients around the world. And while we are proud of this, we continuously ask ourselves the question: how can we improve and extend even more lives in a world of digital and technological change? We are convinced that we can find answers if curious, courageous and team-oriented people are encouraged to question the status quo, make courageous decisions and follow innovative paths. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 367383BR Mar 13, 2023 Switzerland Job Description 5! That’s the number of focus therapy areas for our Global Drug Development team in Novartis and this position is across all 5 being at the heart of our Global Drug Development organization. Imagine the impact you could have as Head Global Program Excellence & Effectiveness. Novartis has one of the largest and broadest drug portfolios across the industry. One of the most business critical roles in the Global Drug Development (GDD) organization is the Global Program Head (GPH) who leads the cross-functional Global Program Team (GPT). In the spirit of creating a functional home for the GPHs, this role is accountable to build and connect a GPH community across Development Units, and to ensure their successful interface with the organization at large. In addition, the role is responsible for supporting and building the team effectiveness capabilities across all GPTs and working closely with other functions (Clinical Development and Clinical Operations) for the effective sub-teams. This entails both scientific content and efficiency of execution across the matrix. Major responsibilities: Your responsibilities include, but are not limited to: • Establish and chair a GPH forum: drive the enterprise mindset and deep understanding of the core GDD operations, collect and convey insights from the GPH community on how well the GDD organization serves the projects, connect GPHs with functions and across Development Units (DUs) • Bring enterprise GPH topics to the GLT and DU Head forum • Coach GPHs to identify and address critical project or operating issues and set the standards for success, key requirements and career development. • Support the GPH selection and project allocation process with a cross GDD perspective • Foster collaboration and communication between GDD and NIBR to enable strategic planning and accelerate the transition of projects into the GDD pipeline • Enable early transition of promising projects/programs across the R&D continuum • Lead a team of internal and external Team Coaches to support Program Teams forming a centre of excellence and capability • Facilitate ongoing sharing and development of measures to elevate effectiveness of various teams in various stages of the development cycle and across all Development Units • Bring a senior and deep development perspective to ensure a faster and more seamless transition of the right projects. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Minimum requirements: What you'll bring to the role: • MD with PhD or other Advanced scientific Degree • ≥10 years pharmaceutical drug development experience covering different disciplines, different therapeutic areas, and spanning across the entire life-cycle from preclinical to post approval; has been part of several successful drug development programs up to approval. • Experienced people leader. Deep understanding of matrix management, leading international and multidisciplinary teams. • Strong relationship builder with experience in stakeholder management; problem-solving, negotiation and conflict resolution skills. • Strong scientific judgment combined with passion for innovation. • Ability to project in the future and convey a strong vision. • Excellent organizational understanding. • Strong connector of ideas and people. Why Novartis? 743 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Global Drug Development Business Unit PORTFOLIO STRATEGY & MGMT GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358254BR Jan 31, 2023 Switzerland Job Description Why join BDSS, Novartis as a Senior QC Specialist?..... .....because in the Biopharmaceutical network we operate as the ‘Launching Machine’ for Novartis Biologics; working to bring our lifechanging medicines from clinical trial stage to market in record time. We are helped do this by facilities and infrastructure that are top class, but also by an environment that is open-minded, and one which supports people to develop with mentoring, training and the opportunity to experience different disciplines. Your main responsibilities: • QC of products & monitoring of processes and facilities • Timely handling & settlement of deviations • Timely update of SOPs • Creation, review and approval of registration documents • Coaching of people • Method Validation • Active participation in project teams/meetings/networks • Active participation in analytical transfer activities • Active participation in Lean Six Sigma Projects • Analytical instrument ownership • No avoidable safety incidents • Cost control and delivering key figures for QC with agreed timelines Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Minimum Requirements • Fluent German • 10 yrs laboratory experience or education as MSc/BSc or PhD • HPLC, capillary electrophoresis, titration • Raw material testing • Microbiology cell banks testing • Thorough knowledge of cGMP requirements • Results oriented, team player and able to work with all levels of the organization • Strong leadership and problem solving skills. Able to identify issues and develop business-friendly solutions in line with the overall compliance Up to 799 million! - that's how many lives we reached with our products in 2022. And while we are proud of this, we continuously ask ourselves the question: how can we improve and extend even more lives in a world of digital and technological change? We are convinced that we can find answers if curious, courageous and team-oriented people are encouraged to question the status quo, make courageous decisions and follow innovative paths. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 361486BR Jan 31, 2023 Switzerland Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Applications are invited for Research Scientists in the Biochemistry group of the Oncology department at NIBR in Basel, Switzerland. The task will be to contribute to the identification and characterization of chemical entities that will become anticancer drugs of the future. We seek for an experienced and motivated associate that will contribute to pushing the boundaries of innovation with bold science by supporting in biochemistry different projects in the innovative field of radio ligand therapy (RLT). Your responsibilities will include: • Development of novel biochemical/biophysical assays using a wide range of technologies, especially SPR and TR-FRET. • Contribution to functional characterization of proteins targets for RLT • While the role will support the NIBR Radioligand Portfolio, the actual work that will be carried out is centered around the profiling of non-radiolabeled compounds and characterization of their mechanism of action • Work in teams in a multi-disciplinary environment and across multi-sites • Presentation of results to teams. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring to the role: Master’s degree (or equivalent, but no PhD/Postdoc) with good knowledge in Biochemistry/Biophysics. • Previous laboratory experience in a similar position in a drug discovery environment will be advantageous • Good hands-on experience in conventional assay technologies used in drug discovery (e.g., FI, TR-FRET, FP) and biophysical methods particularly SPR • Experience in protein-ligand interactions and data analysis with standard curve fitting • Knowledge in lab automation (small laboratory workstations) • Fluent in English (German or French speaking in addition would be an advantage) Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! * This position is eligible for 80-100%* working time, however, some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision NIBR Business Unit Oncology NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 363954BR Feb 28, 2023 Switzerland Job Description 6500! That’s the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Applications are invited for an associate position in an Radioligand therapy (RLT) - Oncology Research laboratory that will carry out cutting-edge research in the area of radioisotope-based therapies together with leading basic research groups within NIBR. The candidate will be participating in drug discovery pharmacology activities performing in vivo pharmacology studies, utilizing a wide range of in vitro and in vivo techniques, like real-time autoradiography, IHC, small animal molecular imaging (PET/SPECT/μCT) and cell-based assays. We seek an experienced, motivated and ambitious associate wishing to continue a successful scientific career in a fast-paced drug discovery environment. The position is based at the Novartis Institutes of BioMedical Research (www.nibr.com) in Basel, Switzerland. The ideal candidate should have a strong hands-on background in in vivo pharmacology, including biodistribution and efficacy evaluation, immunohistochemistry and the molecular imaging modalities, such as PET and SPECT. The successful candidate will perform independent experimentation and data analysis and have solid expertise with rodent in vivo models and is expected to play a key role in the establishment of novel rodent models for Radio Ligand Therapies in the field of cancer. Responsibilities to include but are not limited to: • Perform pre-clinical imaging studies including PET/SPECT/uCT • Perform biodistribution studies and metabolites analysis for novel RLT drug candidates in rodent oncology models • Independently perform and interpret experiments under the leadership of a Lab Head • Propose experimental alternatives, explore and introduce novel technologies and approaches • Use literature and apply it practically • Closely work with multiple teams across expertise groups within Oncology • Consolidate, report data and present in context as needed • Efficiently manage and maintain a functional laboratory, technical equipment and tools Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring to the role: • MSc or BSc (apprenticeship/vocational training) in medical physics, bioengineering, biotechnology, pharmacology or related field • Proficiency and hands-on experience with rodent handling, including oncology models. • Practical work experience in biomedical research from an industry or academic laboratory • Advanced/Fluent English oral and written • Highly collaborative and self-motivated team player • Excellent organizational and communication skills Desirable experience: • Experience with PET/SPECT/uCT imaging with mice and rats; PMOD knowledge would be an advantage • Basic understanding of experimental design, data analysis and interpretation of imaging data • Experience in cellular and molecular biological methods • Experience with immunohistochemical analysis, tissue processing and sectioning • Used to successfully working within a high productivity and quality environment, including Proven ability to effectively collaborate in an interdisciplinary team environment and across sites Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! * This position is eligible for 80-100%* working time, however, some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision NIBR Business Unit Oncology NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 367218BR Mar 10, 2023 Switzerland Job Description 6000! That is the number of associates across the globe in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Genomics Sequencing Technology group, within the Chemical Biology & Therapeutics department in NIBR Basel Switzerland, is seeking a highly motivated and collaborative intern to work on an exciting project in the space of targeted genomics. As part of a dynamic, multidisciplinary team of biologists and data scientist, you have the opportunity to gain insights into cutting-edge technologies in the field of genomics, like gene editing, will have the opportunities to work with colleagues from different platforms and disease areas across NIBR, and will get the chance to develop a general understanding of drug discovery and development, and especially to learn about how we power early-stage drug discovery research with data science. Timing: Latest start date 01.06.2023 Duration: 6 months Your responsibilities: • Design and implement a standardized workflow for targeted genomic sequencing analyses • Explore and structure the requirements of different sequencing strategies • Benchmark existing solutions • Generate structured and informative reports Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Recent Bachelor/Master graduate (less than 6 months relevant work experience) or currently enrolled in a master’s degree with a quantitative background (Bioinformatics, Applied Mathematics, Physics or related field) • Solid programming skills in R and/or Python • Hands-on experience with Linux • Understanding of genomics • Excellent oral and written English Desirable requirements: • Knowledge of gene editing mechanisms • Ability to implement algorithms/methods for reliable workflow integration • Experience with Git (or an alternative version control tool) • Strong data visualization skills Why consider Novartis? 236 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division NIBR Business Unit CBT - NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 361614BR Jan 27, 2023 Switzerland Job Description 105,000 einzigartige Menschen arbeiten bei Novartis, alle mit unterschiedlichen Bedürfnissen und Ambitionen, ausgerichtet auf einen einzigen inspirierenden Zweck: Medizin neu zu definieren für Millionen von Patienten auf der ganzen Welt! Stellenbeschreibung: Ausführung von zugewiesenen Herstellungsaufgaben und -tätigkeiten gemäß dem Produktionsplan, um die rechtzeitige Produktion des Produkts in Qualität und Quantität gemäß den einschlägigen GMP-, Sicherheits- und Umweltrichtlinien zu ermöglichen. Berufserfahrung und Anforderungen: •Teilnahme an den Herstellungsprozessen •Ausführung sämtlich zugewiesener Tätigkeiten gemäß dem Produktionsplan und der gültigen GMP-, Arbeits-, Betriebs-, Umwelt- und Sicherheitsanweisungen und -richtlinien •Ordentliche und rechtzeitige Reinigung, Vorbereitung und Desinfektion der Produktionsanlagen und -räume •Einhaltung und Durchsetzen der Gesundheits-, Sicherheits- und Umweltregeln und -richtlinien (HSE) •Anwendung und Durchsetzen der aktuellen GMP-Regeln •Im Störfall sofortige Maßnahmen ergreifen, Auffälligkeiten an die Manager; Experten und operative Qualitätssicherung melden •Ausführung sämtlich zugewiesener Tätigkeiten gemäß den GMP-, Arbeitsschutz- und Umweltrichtlinien •Falls erforderlich und falls zutreffend, gelegentlich an Wochenenden/Feiertagen arbeiten und planmäßigen Bereitschaftsdienst haben (Schichtbetrieb). Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Minimum Requirements Individuelle Tätigkeiten : •Mindestens 2 Jahre abgeschlossene Berufserfahrung als Gerätebediener oder (vorzugsweise) 5 Jahre in den Bereichen Chemie/Lebensmittel/Arzneimittel/ Biotechnologie/aseptische Herstellung oder Entwicklung •Abgeschlossene Ausbildung zum Chemie- und Pharmatechnologen, Technischer Abschluss; Universitätsabschluss (Chemieingenieurwesen, pharmazeutische Technologie, Biotechnologie, Biochemie) für einige Technologieplattformen erwünscht oder gleichwertige Erfahrung •Grundkenntnisse in Englisch und Beherrschung der Landessprache des Standorts •Anpassungsfähigkeit, Fähigkeit unter Druck zu arbeiten •Beherrschung der GMP-Standards Warum Novartis? Über 799 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir sind davon überzeugt, dass wir Antworten finden können, wenn neugierige, mutige und teamorientierte Menschen dazu ermutigt werden, den Status quo in Frage zu stellen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden gegebenenfalls im Vorstellungsgespräch besprochen. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit CONTRACT MANUFACTURING Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work Yes Apply to JobAccess Job Account

Job ID 359650BR Feb 10, 2023 Switzerland Job Description 90%! Is the percentage of our treatments in development with the potential to be first in class or first in a specific indication! Novartis is deeply committed to transforming the lives of people living with solid tumors. We believe that anyone living with these conditions has the right to a life free from pain, free from symptoms and free from disease - this is our vision for the future. Our mission is to reimagine medicine to extend and improve peoples lives – and our overall company strategy to achieve this is to Focus Novartis as a leading medicine company powered by data science and advanced therapy platforms such as Radioligand Therapy (RLT). Novartis has become the industry leader in RLT after the acquisition of Advanced Accelerator Applications (AAA) and Endocyte in 2018, together with other significant investments to advance radioligand research. Novartis Oncology is now developing a wide range of targeted RLTs, and precision Radioligand Imaging (RLI) agents, for oncology with a rich pipeline targeting multiple tumor types through a phenotypic precision medicine approach. Nuclear Medicine (NM) expertise is key for Novartis Oncology to expand RLT and supportive RLI agents in a sustainable manner. The Clinical Development Medical Director (CDMD) is responsible for leading the planning and management of the assigned RLI clinical program(s) to support the RTL trials from an end-to-end clinical development perspective. As CDMD, you will have oversight of assigned programs and drive execution of the plan. In addition, you will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. Your responsibilities as a Nuclear Medicine expert will include: • Providing clinical leadership and strategic medical input for all clinical results in the assigned project or section of a clinical program • Leading development of RLI related clinical sections of trial and program level regulatory documents • Driving execution of the program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable • Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues • Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas • As a Nuclear Medicine physician specialist, supporting the (Sr.) GPCH or CDH in interactions with external and internal partners and decision boards • Contribute to the publication strategy of RLI/RLT compounds from the scientific standpoint • May work with NIBR (Novartis Institute of Biomedical Research)/ Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you'll bring to the role: • Nuclear medicine Physician/Medical Doctor (EU or US Board certified) • Sophisticated knowledge and clinical training in oncology PET; Clinical practice experience ≥ 5 years preferred. • Experience in Clinical Trials with a PET component • Experience with Radioligand therapy • A consistent track record to interpret, discuss and present data relating to clinical trial(s) with a Nuclear Medicine component • Demonstrated ability to establish effective scientific partnerships with key partners • Solid understanding of GCP, clinical trial design, statistics, regulatory and clinical development processes • Some restrictions to flexible working models may apply and will be discussed at interview if applicable Why consider Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit OHD GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358032BR Mar 05, 2023 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With a strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. Launch HEOR Directors will partner across GDD, TAs, MAP, Regions and priority countries to develop and implement impactful and winning HEOR, IEP and access-relevant evidence generation strategies and tactics such that enable priority countries to secure broad and rapid access, reimbursement, and adoption for priority pre-launch and launch stage IM brands, enhanced healthcare system value proposition and better patient outcomes, and that support new commercial models. Launch HEOR Directors will be responsible to develop and deliver all aspects of the HEOR strategy and execution for priority assets from FDP through launch and post-launch until handover to IBBI. This role will specifically focus on pre-launch and Launch assets residing within International TA teams. With International TAs, early HEOR Directors will co-develop HEOR strategies and tactics with specific focus on priority countries (US, CN, DE, JP), major HTA architypes (e.g., UK/CAN) and Budget Impact archetypes (e.g. Italy and/or Spain) needs and feasibility. They will work in close partnership, collaborate and influence strategic TAs cross-functional teams, GPTs, R&D teams in NIBR & GDD, Region and priority Country teams to maximize patient outcomes and access and healthcare system value for early IM assets. Your responsibilities include, but are not limited to: • Develop and deliver winning HEOR strategy and tactics, with high quality and on-time availability, including outcomes research and other relevant access and healthcare systems evidence and HEOR deliverables (incl. Global Value Dossier, Cost-effectiveness Models, Budget Impact Models, evidence synthesis, PCO or PRO strategy, access-enabling studies, etc.) • Ensure that payer and healthcare needs are reflected into Phase 3b/4, RWE and integrated evidence plans to meet the needs of external experts and institutions involved in reimbursement, pricing, access and healthcare systems decisions. • Collaborate across divisions and functions to ensure effective integration of HEOR and payer evidence deliverables (global value dossiers, cost effectiveness and budget impact models) into integrated product strategies, to enable and support in-country reimbursement submissions / negotiations • Partner closely with Regional and Country teams to design and oversee rollout of global HEOR and payer-evidence strategies and to support local launch preparations and activities concerning access, HEOR, HTA and payer interactions, to achieve reimbursement and other positive funding recommendations and optimal access. • Interact with payers and relevant customer groups in priority countries, gather Country-level insights and feedback, integrate into winning HEOR and payer strategies and tactics, incorporating HEOR perspective in overarching cross-functional product strategies and tactics • Establish and maintains relationships with key economic modelling, outcomes research and HEOR talent and leaders in the field, both outside and inside the company; Stay abreast of external developments, trends and other dynamics that affect the HEOR and HTA domain and competitive position of Novartis assets; share learnings and facilitate hands-on utilization of HEOR deliverables throughout the broader organization. • Support Head of Early HEOR, as well as Head of HEOR & PCO in external engagement (with HTA bodies, policy makers, regulatory agencies, HEOR scientific groups) to shape the HTA environment, the HEOR field and informs the organization on opportunities and risks. • Embrace change, help implement the new ways of working from Transforming for Growth, develop and improve improved ways of working with a focus on flexibility and efficiency. The role can be based in either Switzerland and/or USA. Our selection process will prioritize associates whose roles may be changing or may be impacted as a result of the Transforming for Growth reorganization. For US based candidates: The ideal location for this role is East Hanover, NJ but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific East Hanover, NJ for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 20% travel. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • 8+ years of experience at pharmaceutical companies with at least 5 years in HEOR or RWE role • Advanced Degree; preferably Ph.D., M.D., MBA, RPh or equivalent • Substantial subject matter expertise in HEOR, incl. deep understanding of HEOR and other approaches to generate payer and HCS evidence; preferably subject matter expertise in RWE, capability in designing winning access-relevant RWE studies, analyzing and publishing RWE data and using the results to make impact with access-relevant customers • Valued for customer-centric mindset and passion for delivering value to payers / health systems. Deep understanding of payer/HTA evidence requirements and decision-making dynamic cross countries/regions. Preferably: strong track record in interacting with HTA external stakeholders and active external network with HEOR, RWE and health policy OLs • Highly preferred: operational experience in product launch in priority countries (US, China, Japan, Germany or other Top 10 markets), or at Global or above-country level • Significant experience working in global or above-country multidisciplinary product teams, incl. proven track record in driving implementation of large-scale projects in an agile way; influencing across multiple countries and cross-functional teams; mobilizing, motivating, and coaching country teams in the implementation of global cross-functional launch strategies and tactics • Strong knowledge of research methodology and statistical methods in the field of data analysis, and considerable experience collaborating with quantitative scientists and analysts • Impact-oriented, enterprise and agile mindset with proven track record of fostering innovation, ability to lead in agile organization, and strong process/project management skills #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision PHARMA Business Unit GLOBAL PRODUCT & PORTFOLIO STRATEGY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Alternative Location 2 Ireland Alternative Location 3 United Kingdom Functional Area Market Access Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 366494BR Mar 06, 2023 Switzerland Job Description Do you find economic relationships just as exciting as the services provided by companies in the healthcare sector? You are looking for a training opportunity that combines technical and methodical knowledge with practical know-how from the healthcare industry? This is your chance to apply for our cooperative study program in BWL- Healthcare Management together with the Duale Hochschule Baden-Württemberg! Duration: 01.10.2023 – 30.09.2026 This is our offer: • Insights into different departments within a multinational company, like e.g. Human Resources, Marketing, Finance or healthcare specific topics like Market Access or Global Health • Transfer of knowledge into practical experience in our departments during the practical phases (3 months rhythm) • Studies at the DHBW (Dualen Hochschule Baden-Württemberg) in Lörrach, mainly consistent of BWL (business administration) classes like controlling, human resources, law and general economic topics but also with a strong focus on health systems, medical controlling, health policy and medicine for non-medical people • Graduation after 3 years (6 semesters) in Bachelor of Arts – BWL-Healthcare Management • Salary will be paid during the whole duration of study Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • General University Entrance Qualification (with additional successful DELTA-Examination from DHBW), Abitur or Matura • High willingness to perform • High degree of independency and flexibility • Good team worker • Very good knowledge in English and German Why Novartis? 236 million. That’s how many lives our products touched in 2022 and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division CTS Business Unit HR NBS Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 365504BR Mar 08, 2023 Switzerland Job Description 1886! Wir haben mehr als 130 Jahre Erfahrung in der Behandlung von Patienten. Sandoz, ein Geschäftsbereich von Novartis, ist ein weltweit führender Anbieter von Generika und Biosimilars, der sich dafür einsetzt, den Zugang zu Medikamenten weltweit zu fördern! Der Medical Sales Representative ist verantwortlich für das Erreichen der Verkaufsziele und die Bewerbung der Produkte bei Apothekern und anderen Health Care Professionals für die zugewiesene Region. Aufgaben: • Sachkundige Beratung und Betreuung von Apotheken sowie Ausbau von Kundenpotenzialen • Unterstützt die Entscheidungsfindung von HCPs zur Optimierung von Patientenergebnissen durch die Bereitstellung der relevanten Daten, Schlüsselbotschaften und Krankheitsinformationen • Nutzt alle verfügbaren Datenquellen um Gebiets- und Kundenbindungspläne zu erstellen, adaptieren und priorisieren • Unterhält ein fundiertes und aktuelles Wissen über Industrie, therapeutisches Gebiet, Mitbewerber und Käuferdynamik und konzentriert sich auf prioritäre Kundenchancen • Nutzt Methoden zur Kundenbindung vollumfänglich um qualitativ hochwertige Kundeninteraktionen zu erstellen und damit das Kundenerlebnisses zum Wohle der Patienten zu maximieren • Verhält sich entsprechend ethischen Richtlinien, behördliche Auflagen und Sandoz Werten und Verhaltensweisen • Meldet technische Beschwerden, unerwünschten Ereignissen, Sonderfall-Szenarien im Zusammenhang mit Sandoz-Produkten innerhalb von 24 Stunden nach Erhalt Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Anforderungen: • Deutsch obligatorisch. Französisch von Vorteil • 3-4 Jahre Erfahrung im Verkauf oder Vertrieb, vorzugsweise in der pharmazeutischen Industrie • Erfahrung im Key Account Management wünschenswert • Erfahrung in der Produkteinführung wünschenswert • Etabliertes Netzwerk zur gezielten Kundengruppe (Apotheken) wünschenswert • Hohe Reisebereitschaft innerhalb der zugewiesenen Region • Fahrausweis Klasse B Why Sandoz? 500 million patients were touched by Sandoz generic and biosimilar medicines in 2021 and while we’re proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world. How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Sandoz! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Group Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision SANDOZ Business Unit COMMERCIAL OPS EUROPE SZ Location Switzerland Site Bern Company / Legal Entity Sandoz Pharmaceuticals AG Functional Area Sales Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 362863BR Jan 26, 2023 Switzerland Job Description We are looking for people with the right technical skills to support our QC team in Novartis, Stein. What will you do? • Evaluation and procurement of analytical systems for the routine use of a wide variety of measurement methods (determination of physical parameters, spectroscopy, chromatography,...). • Planning, execution and documentation of the qualification of computerised analytical systems (IQ/OQ/PQ) under GMP conditions. • Introduction of analytical systems in quality control (method development/management, user management, creation of SOPs, training, ensuring of maintenance and calibration). • Support of the technical QC team in equipment live cycle management (system changes, evaluation of validation status, data integrity improvements, decommissioning). • Order placement and monitoring of service orders for IT service providers. Cost and deadline monitoring of your own projects. • Implementation of local projects for the digitization of the QC processes. Participation in local and global project teams for the introduction of new QC data processing systems (e.g. CDS, LIMS) . Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements -Project Management -Technical knowledge -German language, written/ spoken 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives.Division Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 367072BR Mar 09, 2023 Switzerland Job Description Are you are a goal-oriented individual with a strong team-player mindset that likes to work in complex environments? Then you might be the perfect fit – join our amazing team in NTO and help us reimagine medicine! You will support Stein Steriles MU Galenic in process-related matters with the goal to continuously optimize manufacturing operations in terms of quality and efficiency. This role is an ideal entry point into a GMP environment and will allow you to gain insight into a broad spectrum of activities in a state-of-the-art clean room environment. Preferred start date: As soon as possible, preferably 01.04.2023 Latest start date: Flexible, preferred 01.05.2023 Duration: 12 months with potential contract extension Your responsibilities: • General support of manufacturing operations • Establishment and maintenance of standard operating procedures • Deviation handling including root cause investigation in interaction with involved stakeholders • Insight in batch record review and complaint management #LI-Onsite Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • University degree in Science, Pharmacy, Biology or Chemical Engineering, Pharmaceutical Technology or equivalent • Fluent German and English language knowledge (spoken and written). Communication language in Stein is German. • Learning agility, flexibility and good communication skills • Team player with strong team spirit; open for feedback Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Novartis Technical Operations Business Unit LARGE MOLECULES Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 367989BR Mar 21, 2023 Switzerland Job Description Als Reliability Engineer (m/w/d) im Asset Life Cycle Managment sind Sie verantwortlich für strategische Instandhaltung und Prozessoptimierung. Im Team wird die stategische Instandhaltung durch stetige datenanalysen optimiert und durch neue technologien oder herangehensweisen weiterentwickelt. Mithilfe Ihres Know-how und Ihrer Begeisterung für Technik unterstützen Sie die Produktionsbetriebe durch Prozessoptimierung und Potenzialanalysen die Anlagenverfügbarkeit und -leistungsfähigkeit zu verbessern. Aufgaben • Analyse verfahrenstechnische Anlagen auf Potenziale zur Optimierung im Bereich Betrieb und Technik – OAE/OEE • Durchführen von Kritikalitätsanalysen der technischen Anlagenstruktur und von Risikobewertungen • Experte in Investitionsprojekten zur Implementierung der ALCM Strategie • Optimierung und Weiterentwicklung der Instandhaltungsstrategien auf die individuellen Anforderungen der Produktionsbetriebe • Durchführung von Root-Cause-Analysen zur technischen Optimierung der Anlagen • Aufbau, Optimierung und Unterhalt der technischen Reportingstruktur durch die Entwicklung von Dashboards und weiteren Tools • Definieren, Auswertung und Trending von Asset Life Cycle Managment KPI’s • Austausch mit den Produktionsbetrieben und Betriebs-Engineering zur stetigen Weiterentwicklung des Leistungsportfolios und vermitteln ihr Fachwissen im Reliability Management an die Kollegen • Erstellung und Unterhalt von Arbeitsanweisungen (SOP) Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Ein erfolgreich absolviertes Studium der Ingenieurswissenschaften oder vergleichbares Studium der Wirtschaftswissenschaften mit technischem Schwerpunkt und ein ausgeprägtes technisches Verständnis (FS, Dipl. Ing. / M. Sc. / B. Sc.). • >5 Jahre Berufserfahrung im Bereich der Prozessindustrie mit fundierten Erfahrungen in der Prozessoptimierung und Instandhaltung inkl. MROM • Kenntnisse im Projektmanagement • Sehr gute Kenntnisse in SAP-PM/MM, MS Office und COMOS • Fundierte GMP & Compliance Kenntnisse von Vorteil • Analytische und strukturierte Arbeitsweise mit einem hohen Maß an Selbstständigkeit • Hervorragende kommunikative Eigenschaften auf allen Hierarchieebenen runden Ihr Profil ab • Sprache: Deutsch und Englisch 743 Millionen! Das ist die Gesamtzahl der Patienten, die wir im Jahr 2022 durch unsere gemeinsamen Bemühungen, die Medizin neu zu gestalten und das Leben von Patienten auf der ganzen Welt wirklich zu verbessern, erreicht haben. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir sind davon überzeugt, dass wir Antworten finden können, wenn neugierige, mutige und teamorientierte Menschen dazu ermutigt werden, den Status quo in Frage zu stellen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden ggf. im Vorstellungsgespräch besprochen. Tritt unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu deiner Erfahrung oder deinen Karrierezielen passt, du aber in Kontakt bleiben möchtest, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, kannst du hier dem Novartis Netzwerk beitreten: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit SITE DEVELOPMENT Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 365155BR Feb 22, 2023 Switzerland Job Description 28.000 Mitarbeiter aus mehr als 100 Ländern! 150! Unser Werk Novartis Stein ist einer der wichtigsten Standorte für innovative, hochqualitative Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Um Novartis Technical Operations zu verstärken, suchen wir derzeit eine(n) QC Analyst I. Diese Stelle ist auf maximal 2 Jahre befristet. Ihre Haupttätigkeiten: • Organisation, Durchführung, Auswertung und Dokumentation von mikrobiologischen Routine- Bioburdentests von sterilen Produkten unter Einhaltung der GMP-Regeln, QMs, SOPs und GSU- Vorschriften • Instandhaltung des Laborbereiches nach 5/6S • Pflege und Betrieb der Geräte und Einrichtungen • Entsorgungsmanagement von Laborabfällen • Lagerhaltung/ Pflege Kanban System • Materialmanagement und Reinigung Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie zur Rolle mitbringen: • Abgeschlossene Lehre als Laborant/in oder äquivalente Ausbildung • Erfahrung in der Pharmaindustrie (Qualitätssicherung, Produktion steriler Formen) • Erfahrung in mikrobiologischer Analytik • Deutsch: fliessend (mündlich/schriftlich) • Englisch: Grundkenntnisse Wünschenswerte Anforderungen: • Gute Computerkenntnisse (MS Office etc.) • Hohes Maß an Selbstständigkeit und Organisationsfähigkeit Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Engagement für Vielfalt & Inklusion Novartis ist bestrebt, ein hervorragendes, integratives Arbeitsumfeld und ein vielfältiges Team aufzubauen, das die Patienten und Gemeinschaften, denen wir dienen, repräsentiert. Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 368457BR Mar 22, 2023 Switzerland Job Description 28,000 associates of more than 100 nationalities! Deliver high quality and affordable medicine on time, every time, safely and efficiently. Be part of an important QA Group releasing products with high quality and take opportunity to learn the responsibilities of a QA function. This position is limited for 24 months. Your key responsibilities: • Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity & eCompliance • Support exception investigations as QA responsible.. • Review & approval of production records (executed BR) • MBR review • Reporting of deviations within defined timelines Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Bachelor in science or at least 3 to 5 years in manufacturing or laboratory are with respective apprenticeship • 3-5years experience in Pharma/Manufacturing sector in analytical lab in a GMP environment/equivalent Expertise in GxP operations Able to understand changing dynamics of Pharmaceutical industry • Fluent in English and German • Knowledge in aseptic processing/sterile manufacturing or laboratory environment • Knowledge in GMP, good documentation practice, eCompliance and Data Integrity You’ll receive: Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, Unlimited learning and development opportunities. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve. Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Part Time Part Time percentage 50 Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 364979BR Feb 22, 2023 Switzerland Job Description 80 Millionen! Das ist die Anzahl der sterilen Produkte, die in unserer Produktionsstätte pro Jahr verarbeitet werden. Als Teil der Qualitätskontrolle spielst du eine Schlüsselrolle bei der Analytik des wichtigsten Hilfsstoffes – Wasser – all unserer sterilen Produkte und trägst zur höchsten Produktqualität für Millionen von Patienten in mehr als 150 Ländern auf der ganzen Welt bei. Wir suchen eine(n) motivierte(n) Mitarbeiter*in in unserer Qualitätskontrolle für den Bereich Wasseranalytik und Bakterien Endotoxin Testung. Diese Position ist befristet auf 24 Monate. Ihre Haupttätigkeiten: • Bearbeitung von Abweichungen im Bereiche der Analytik von Bakterien Endotoxinen und Wasseranalytik (physikalisch-chemisch und mikrobiologisch) • Schreiben und Überprüfung von Standardarbeitsanweisungen • Schreiben und Überprüfung von Validierungsplänen und -berichten • Planung und Durchführung von Gerätequalifizierungen • Fungiert als Spezialist für den o.g. Aufgabenbereich bei Behörden- und Kundeninspektionen • Aufrechterhaltung und Verbesserung schlanker Prozesse und des Informationsflusses innerhalb des Teams Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie zur Rolle mitbringen: • Mindestens Bachelor/Master in Life Sciences oder äquivalent • Erfahrung im Bereich Qualitätskontrolle und/oder Berufserfahrung im GMP/GxP Umfeld • Erfahrung im Bereich der Wasseranalytik/ Bakterienendotoxine wünschenswert • Sehr gutes technisches und analytisches Verständnis • Ausgeprägtes Qualitätsdenken und gewinnende Kommunikationsfähigkeit im Umgang mit verschiedenen internen Ansprechpartnern • Fliessend Deutsch und Englisch Kenntnisse • Teamplayer, exakte und selbständige Arbeitsweise • Hohe Eigenverantwortlichkeit und hohe Lernbereitschaft Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Engagement für Vielfalt & Inklusion Novartis ist bestrebt, ein hervorragendes, integratives Arbeitsumfeld und ein vielfältiges Team aufzubauen, das die Patienten und Gemeinschaften, denen wir dienen, repräsentiert. Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 364985BR Feb 22, 2023 Switzerland Job Description 80 Millionen! Das ist die Anzahl der sterilen Produkte, die in unserer Produktionsstätte pro Jahr verarbeitet werden. Als Teil der Qualitätskontrolle spielst Du eine Schlüsselrolle bei der Analytik des wichtigsten Hilfsstoffes – Wasser – all unserer sterilen Produkte und trägst zur höchsten Produktqualität für Millionen von Patienten in mehr als 150 Ländern auf der ganzen Welt bei. Diese Position ist temporär für 24 Monate. Ihre Haupttätigkeiten: • Organisation, Durchführung, Auswertung und Dokumentation der Analytik von Wasser mit Hilfe physikalisch-chemischer, biologischer und mikrobiologischer Tests • Einhaltung und Überwachung der cGMP-Regeln, SOPs (Standardarbeitsanweisungen) und Sicherheits-Vorschriften • Verantwortlichkeit für Laborequipment im zugeteilten Bereich • Mithilfe bei Abklärungen von OOS/OOE-Resultaten und Abweichungen • Mithilfe bei der Vorbereitung von Behörden- und Kundeninspektionen • Aufrechterhaltung und Verbesserung schlanker Prozesse und des Informationsflusses innerhalb des Teams Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie zur Rolle mitbringen: • Abgeschlossene Lehre als Laborant/in oder äquivalente Ausbildung • Erfahrung im Bereich Qualitätskontrolle und/oder Berufserfahrung im GMP/GxP Umfeld • Erfahrung im Bereich der Wasseranalytik wünschenswert • Sehr gutes technisches und analytisches Verständnis • Ausgeprägtes Qualitätsdenken und gewinnende Kommunikationsfähigkeit im Umgang mit verschiedenen internen Ansprechpartnern • Fliessend Deutsch. Englisch Kenntnisse (Wort und Schrift) • Teamplayer, exakte und selbständige Arbeitsweise • Hohe Eigenverantwortlichkeit und hohe Lernbereitschaft Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Engagement für Vielfalt & Inklusion Novartis ist bestrebt, ein hervorragendes, integratives Arbeitsumfeld und ein vielfältiges Team aufzubauen, das die Patienten und Gemeinschaften, denen wir dienen, repräsentiert. Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 366904BR Mar 08, 2023 Switzerland Job Description 28.000 Mitarbeiter aus mehr als 100 Ländern! 150! Unser Werk Novartis Stein ist einer der wichtigsten Standorte für innovative, hochqualitative Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Um Novartis Technical Operations zu verstärken, suchen wir derzeit eine(n) QC Analyst I. Diese Stelle ist auf maximal 9 - 12 Monaten befristet. Ihre Haupttätigkeiten: • Organisation, Durchführung, Auswertung und Dokumentation von mikrobiologischen Routine- Bioburdentests von sterilen Produkten unter Einhaltung der GMP-Regeln, QMs, SOPs und GSU- Vorschriften • Instandhaltung des Laborbereiches nach 5/6S • Pflege und Betrieb der Geräte und Einrichtungen • Entsorgungsmanagement von Laborabfällen • Lagerhaltung/ Pflege Kanban System • Materialmanagement und Reinigung Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie zur Rolle mitbringen: • Abgeschlossene Lehre als Laborant/in oder äquivalente Ausbildung • Erfahrung in der Pharmaindustrie (Qualitätssicherung, Produktion steriler Formen) • Erfahrung in mikrobiologischer Analytik • Deutsch: fliessend (mündlich/schriftlich) • Englisch: Grundkenntnisse Wünschenswerte Anforderungen: • Gute Computerkenntnisse (MS Office etc.) • Hohes Maß an Selbstständigkeit und Organisationsfähigkeit Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Engagement für Vielfalt & Inklusion Novartis ist bestrebt, ein hervorragendes, integratives Arbeitsumfeld und ein vielfältiges Team aufzubauen, das die Patienten und Gemeinschaften, denen wir dienen, repräsentiert. Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 368300BR Mar 21, 2023 Switzerland Job Description 135,000 Novartis associates in 140 countries worldwide share the vision of a better today and tomorrow for patients – a vision that drives our growth and success. The QC microbiology department at the Stein site in Switzerland supports both the sterile and the solids plant with globally recognized experts who are open to all microbiological and biological questions. As support for our team, we are looking for a committed postgraduate in the field of QC microbiology who will work in a dynamic and challenging technical GMP environment as of June 1st, 2023 (for 12 months). Preferred start date: 01.06.2023 Latest start date: 01.07.2023 Duration: 12 months Your responsibilities: • Lab coordination • Single point of contact (SPOC) for the costumers of the laboratory. Due date communication • Sample storage and management • Generation and review of lab documents • Administrative work in the lab • Analytical testing/documentation of drug product and finished product and complaints • Stability and packaging material samples to GxP standards Stability • Analytical documentation of stability samples to GxP standards Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Bachelor/Master graduate in Pharmaceutical, Biotechnical, Chemical, Analytical studies or/and life sciences • Full proficiency in German and English is a must • GxP experience preferred, not a must • Team player • Good time management • Interest in Quality Assurance • Microbiological basic understanding Why Novartis? 743 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 362854BR Mar 07, 2023 Switzerland Job Description 10 days! That is how long we in Cell & Gene Therapy treat a patient’s T-cells, before returning them with the potential to save a patient’s life. This is a unique and novel personalized treatment where we work with the patient’s own cells during our production process. Not only are re imagining medicine but we are also impacting on, saving and improving quality of life. As a Senior Engineer - Multidiscipline you are responsible for executing engineering activities within technical area of expertise by using reliable and cost effective technical solutions, ensuring technical quality to enable the overall site / project objectives. Join us! Major accountabilities: • Responsible for Engineering activities including planning and coordination of maintenance & calibration activities. • Supporting internal and external audits. • Leading root cause investigation for product deviations, recalls. • Troubleshooting management. • Spare parts management. • Provide frontline support for technicians. • Deviation / Action / CAPA and Quality event management. • Technical change request management. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • 3-5 years of experience in Pharma/Manufacturing sector in analytical lab in a GMP environment. • Fluency in English and German language. • Capability of managing performance improvement and business continuity. • Having a business mindset and stakeholder engagement skills. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit SITE DEVELOPMENT Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 367922BR Mar 20, 2023 Switzerland Job Description 28.000 Mitarbeiter aus mehr als 100 Ländern! Liefern Sie qualitativ hochwertige und erschwingliche Medikamente pünktlich, jederzeit, sicher und effizient. Diese Rolle beinhaltet die GMP-konforme, effiziente und termingerechte Durchführung und Dokumentation der analytischen Arbeiten von medizinischen Produkten. Selbstständige Durchführung von Routineanalysen unter exakter Einhaltung der Analysenvorschriften und Standard Operating Procedures (SOPs). Ihre Haupttätigkeiten: • Dekontamination aller potenziell kontaminierten Verbrauchsmaterialien. • Waschen, Verpacken und Sterilisation von Glaswaren und anderen Labormaterialien. • Entsorgung von Einwegartikeln und gebrauchten Nährmedien unter Einhaltung der Sicherheitsvorschriften. • Bereitstellung von Materialien für alle Teams von QC Microbiology. • Überwachung der Reserven an Glaswaren und weiteren Labormaterialien. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie zur Rolle mitbringen: • Abgeschlossenen Schulausbildung • Strukturiertes Arbeiten • Konsequent die Einhaltung der GMP-, GSU- Richtlinien, SOPs und GSU- Vorschriften verfolgen. (GSU=Gesundheit Sicherheit Umwelt) • Suchen und Implementierung von Optimierungsmöglichkeiten zur Kostenreduktion. Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 352828BR Nov 03, 2022 Switzerland Job Description 10 ! days - that is how long we in Cell & Gene Therapy treat a patient’s T-cells, before returning them with the potential to save a patient’s life. This is a unique and novel personalized treatment where we work with the patient’s own cells during our production process. Not only are re imagining medicine but we are also impacting on, saving and improving quality of life. As a Cell Processing Specialist you will play an important role in this process by being responsible for operations on Day 0, cell washing and harvest processing and for verifying cell processing associates on intermediate processing days of patient derived clinical and commercial cellular immunotherapy products. You will also managed formulation and verification of all media lots. Due to the nature of the starting material (patient cells) this role requires high level of proficiency and ownership of the process and media formulation. Your responsibilities include, but are not limited to: • Ownership for the processing of the assigned patient starting material in the clean room environment. • Ability to gown aseptically and work in a clean room environment (ISO 8, 7 and ISO 5) areas for extended periods of time. • Day 0, cell washing and Harvest processing with the ability to work with automated equipment such as the CS5 and Sepax • Verification of intermediate process days which include expertise with the wave bioreactor, NC-200 and in process environmental monitoring • Maintains and prepares equipment/environment for use • Proficient in the use of production related IT systems such as SAP, LIMS and MES • Documents all steps in the assigned Batch record in line with GMP requirements • Conduct all necessary processing/verification steps for the assigned lot with highest skill level of aseptic technique. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Minimum of 1-2 years experience in cGMP or academic or lab setting with aseptic or cell culture experience required • Apprenticeship or Bachelor's Degree in relevant Engineering or Scientific discipline (e.g. Biology or Laboratory Assistant) • Ability to perform complex calculations and an understanding of scientific notations • Fluent in writing and speaking in English & German Over 799 million! - that's how many lives we reached with our products in 2021. And while we are proud of this, we continuously ask ourselves the question: how can we improve and extend even more lives in a world of digital and technological change? We are convinced that we can find answers if curious, courageous and team-oriented people are encouraged to question the status quo, make courageous decisions and follow innovative paths. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit NTO CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 352046BR Sep 15, 2022 Switzerland Job Description 2 Milliarden! So viele Tabletten, Kapseln, Ampullen, Fertigspritzen, Fläschchen, Autoinjektoren und transdermale therapeutische Systeme werden jedes Jahr in Stein hergestellt und in mehr als 150 Länder geliefert. Als ein Operator in der Produktion haben Sie die Möglichkeit, einen Beitrag zur Verbesserung des Lebens von Patienten zu leisten. Kommen Sie noch heute zu uns und werden Sie Teil eines innovativen, vielseitigen und erfolgreichen Unternehmens - machen Sie den Unterschied! Als Equipment Operator werden sie zustaending fuer die Ausführung von zugewiesenen Herstellungsaufgaben und -tätigkeiten gemäß dem Produktionsplan, und die rechtzeitige Produktion von unseren Produkten in Qualität und Quantität gemäß den einschlägigen GMP-, Sicherheits- und Umweltrichtlinien zu ermöglichen. Ihre Hauptaufgaben: • Teilnahme an den Herstellungsprozessen • Ausführung sämtlich zugewiesener Tätigkeiten gemäß dem Produktionsplan und der gültigen GMP-, Arbeits-, Betriebs-, Umwelt- und Sicherheitsanweisungen und -richtlinien • Rechtzeitige und fehlerfreie Überprüfung der Chargendatensätze (Teil der Produktion) • Ordentliche und rechtzeitige Reinigung, Vorbereitung und Sterilisierung der Produktionsanlagen und -räume • Verantwortung für die Haushaltsführung des Produktionsbereichs (Reinigung, Ordnung, 5S....) • Einhaltung und Durchsetzen der Gesundheits-, Sicherheits- und Umweltregeln und -richtlinien (HSE) • Anwendung und Durchsetzen der aktuellen GMP-Regeln • Probenahme, Aliquotierung, Verteilung und Durchführung von prozessbegleitenden Kontrollen • Falls zutreffend, delegierte Umweltüberwachung für Reinräume und delegierte Probenahmen von Reinstwasser und Reindampf durchführen • Sicherstellung/Überwachung einer ordnungsgemäßen Funktionstüchtigkeit der Anlagen, um frühzeitige Anzeichen von Anomalien zu erkennen. Im Störfall geeignete Maßnahmen ergreifen. • Exzellente Dokumentation der Maßnahmen, gemäß den GMP-Vorschriften • Verwaltung der Verbrauchsmaterialversorgung, die für das ordnungsgemäße Funktionieren des Betriebs erforderlich ist (z. B. Filter, Harze, Anschlüsse, Beutel, Reagenzien, Gas, WCB usw.). • Tägliche Überprüfung von Produktionsanlagen, Hilfsgeräten und Räumen • Klare und genau Dokumentierung der notwendigen Anmerkungen klar in Chargendatensätze • Falls erforderlich und falls zutreffend, gelegentlich an Wochenenden/Feiertagen arbeiten und planmäßigen Bereitschaftsdienst haben. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Erfahrung (vorzugsweise) in den Bereichen Chemie/Lebensmittel/Arzneimittel/ Biotechnologie/aseptische Herstellung oder Entwicklung • Technischer Abschluss; Universitätsabschluss (Chemieingenieurwesen, pharmazeutische Technologie, Biotechnologie, Biochemie) für einige Technologieplattformen erwünscht oder gleichwertige Erfahrung • Fliessend Deutsch/ Grundkenntnisse in Englisch. Über 799 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir sind davon überzeugt, dass wir Antworten finden können, wenn neugierige, mutige und teamorientierte Menschen dazu ermutigt werden, den Status quo in Frage zu stellen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit NTO SMALL MOLECULES Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 361618BR Feb 15, 2023 Switzerland Job Description 18 – die Anzahl an unterschiedlichen Biotech-Molekülen, die aktuell in unserem Labor analysiert werden. Das Laborteam besteht aus 25 – 30 Mitarbeitern. Es handelt sich um eine befristete Stelle, die auf 2 Jahre begrenzt ist. What will you do? • Umgang mit einem zukunftsorientierten Biotech Produkte Portfolio und modernster Analyse-Technologien. Im Fokus stehen Bioanalytik mittels HPLC und CE. • Organisation, Durchführung, Auswertung und Dokumentation der chemisch und physikalischen Testung von biotechnologischen Produkten im Rahmen von Freigaben und Stabilitätsstudien für Stein Steriles und weiteren Auftraggebern • Organisation, Durchführung, Auswertung und Dokumentation von Methodenvalidierungen neuer Launch-Produkte sowie laborspezifischer Validierungen • Einhaltung und Überwachung der cGMP-Regeln, SOPs (Standard Operating Procedure) und Sicherheits-Vorschriften • Verantwortlichkeiten für Laborequipment im zugeteilten Bereich • Mithilfe bei Abklärungen von OOS/OOE-Resultaten und Deviations • Mithilfe bei der Vorbereitung von Behörden- und Kundeninspektionen • Aufrechterhaltung schlanker Prozesse und des Informationsflusses innerhalb des Teams What you’ll bring to the role: • Abgeschlossene Lehre als Laborant/in oder äquivalente Ausbildung • Erfahrung im Bereich Qualitätskontrolle und/oder Berufserfahrung im GMP/GxP Umfeld • Erfahrung mit den Analysentechniken HPLC, UV Spektroskopie, pH, Wasser mittels Karl-Fischer, CU und weitere physikalische Tests • Sehr gutes technisches und analytisches Verständnis • Ausgeprägtes Qualitätsdenken und gewinnende Kommunikationsfähigkeit im Umgang mit verschiedenen internen Ansprechpartnern • Fliessend Deutsch. Englisch Kenntnisse (Wort und Schrift) • Teamplayer, exakte und selbständige Arbeitsweise, detailorientiert • Hohe Eigenverantwortlichkeit und hohe Lernbereitschaft Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Erfahrung in der Bioanalytik wünschenswert (SE-HPLC, CEX-HPLC, RP-HPLC, HI-HPLC, CE, SDS-Page) • Sicherer Umgang mit MS Office, SAP und Chromatographie Systemen von Vorteil Warum Novartis? Über 799 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir sind davon überzeugt, dass wir Antworten finden können, wenn neugierige, mutige und teamorientierte Menschen dazu ermutigt werden, den Status quo in Frage zu stellen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden gegebenenfalls im Vorstellungsgespräch besprochen. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 357281BR Nov 11, 2022 Switzerland Job Description QC Analyst II, Novartis, Stein, Switzerland 18! Die Anzahl an unterschiedlichen Biotech-Molekülen, die aktuell in unserem Labor analysiert werden. Das Laborteam besteht aus 25 – 30 Mitarbeitern. Durch die Notzulassung des SKO136 Produktes brauchen wir Verstärkung innerhalb des QC Biocenter of Excellence l Labors um einen wesentlichen Beitrag zur Bekämpfung der Pandemie zu leisten. Diese Position is gesucht für 18 Monaten. Zu Ihren Aufgaben gehören unter anderem: • Umgang mit einem zukunftsorientierten Biotech Produkte Portfolio und modernster Analyse-Technologien. Im Fokus stehen Bioanalytik mittels HPLC und CE • Organisation, Durchführung, Auswertung und Dokumentation der chemisch und physikalischen Testung von biotechnologischen Produkten im Rahmen von Freigaben und Stabilitätsstudien für Stein Steriles und weiteren Auftraggebern • Organisation, Durchführung, Auswertung und Dokumentation von Methodenvalidierungen neuer Launch-Produkte sowie laborspezifischer Validierungen • Einhaltung und Überwachung der cGMP-Regeln, SOPs (Standard Operating Procedure) und Sicherheits-Vorschriften • Verantwortlichkeiten für Laborequipment im zugeteilten Bereich • Mithilfe bei Abklärungen von OOS/OOE-Resultaten und Deviations • Mithilfe bei der Vorbereitung von Behörden- und Kundeninspektionen • Aufrechterhaltung schlanker Prozesse und des Informationsflusses innerhalb des Teams Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie mitbringen werden: • Abgeschlossene Lehre als Laborant/in oder äquivalente Ausbildung • Erfahrung im Bereich Qualitätskontrolle und/oder Berufserfahrung im GMP/GxP Umfeld • Erfahrung mit den Analysentechniken HPLC, UV Spektroskopie, pH, Wasser mittels Karl-Fischer, CU und weitere physikalische Tests • Sehr gutes technisches und analytisches Verständnis • Ausgeprägtes Qualitätsdenken und gewinnende Kommunikationsfähigkeit im Umgang mit verschiedenen internen Ansprechpartnern • Fliessend Deutsch. Englisch Kenntnisse (Wort und Schrift) • Teamplayer, exakte und selbständige Arbeitsweise, detailorientiert • Hohe Eigenverantwortlichkeit und hohe Lernbereitschaft Warum Novartis? 799 Millionen! - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. Engagement für Vielfalt und Inklusion: Novartis setzt sich für Vielfalt, Chancengleichheit und Integration ein. Wir engagieren uns für den Aufbau vielfältiger Teams, die repräsentativ für die Patienten und Gemeinschaften sind, denen wir dienen, und wir streben danach, ein integratives Arbeitsumfeld zu schaffen, das mutige Innovationen durch Zusammenarbeit fördert und unsere Mitarbeitenden befähigt, ihr volles Potenzial zu entfalten. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden gegebenenfalls im Vorstellungsgespräch besprochen. Werden Sie Mitglied in unserem Novartis Netzwerk: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 352755BR Mar 14, 2023 Switzerland Job Description 80million! This is the number of sterile products that are processed in our workplace per year. As part of the production team, you will play a key role in manufacturing and ensuring the highest product quality for millions of patients in more than 150 countries around the world. For the Process Unit (PU) Galenic we are looking for a motivated and committed postgraduate for 12 months who would like to gain an insight into the role of the process expert in sterile production and actively support us. Preferred start date: as soon as possible Duration: 12 months Your responsibilities will include: • Support in the investigation and processing of manufacturing deviations and CAPA management • Identification of process weaknesses and assistance in process improvement projects • Create and update of SOPs / FRMs • Assistance in the planning and implementation of cleaning validation and thermal requalification • Assistance in documentation preparation and processing of risk analysis and change requests • Supporting sample dispatch #LI-Onsite #LI-Hybrid Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Scientific or pharmaceutical studies (Bachelor/Master) which you have completed in the past 12 months • Very good knowledge of English and German • Ability to work in a team and flexibility Why Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Novartis Technical Operations Business Unit LARGE MOLECULES Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 352823BR Jan 16, 2023 Switzerland Job Description 10 ! days - that is how long we in Cell & Gene Therapy treat a patient’s T-cells, before returning them with the potential to save a patient’s life. This is a unique and novel personalized treatment where we work with the patient’s own cells during our production process. Not only are we re imagining medicine but we are also impacting on, saving and improving quality of life. As a Senior QA Specialist CGT not only will be part of this but you will also be a member of the QA Operations Team that is responsible for the overall quality oversight of the production and other operational units within Stein C> manufacturing, e.g. Quality Control (QC). The team ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the operational units. Core activities of the team QA Operations expert includes: • QA oversight of the production/shopfloor and QC laboratories • Approval of manufacturing deviations • Approval of analytical deviations and OOS/OOE records • Support of QA release of the final product Responsibilities include: • Independent, flexible processing of activities supporting the release of analytical results of raw materials, media, apheresis and finished product (e.g. CoA signature, Batch record review, CoC, Max Dose review...) • Collaboration with Team Leader and management to provide direction, define strategies and make decisions. Supporting to achieve the strategic objectives, where applicable. • Manage OOS/OOE records, SSFs, Deviations, CAPAs, also with higher complexity and impact, in a reliable and efficient manner. Provide ad hoc decisions and act as advisor in day-to-day operations • Manage Exceptional Provisions and Global GxP Escalations • Independent, flexible processing of all activities related to the Aseptic Operator Qualification (AOQ) and Aseptic Process Validation (APV), provide guidance on aseptic questions • Ensures feasible and beneficial monitoring of processes and product related KQIs, reports to Site and Global Management, and identifies room for improvement. • General Quality Oversight and Review/Approval of Lab Documents/Journals/Lot and release documentation. This includes raw materials/starting materials, vector, apheresis, IPCs, QC samples and finished product • Author/Reviewer/Approver of SOPs/WPs/FRMs, • Audit and Inspection support, validation reports, transfer documents, stability reports, APR/PQR, change control. Pls note: this is temporary position/ Novartis contract duration is for 2 years. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Master of Science in Biology, Biochemistry, Microbiology or related (or equivalent). • Good understanding of cGMP • Fluent English, German skills desired, strong written and verbal communication skills • 5+ years of experiences in pharmaceutical QA, QC or production environment • IT-Knowledge (MS Office, SAP, Trackwise, MES) • Ability to communicate clearly with a variety of individuals across different departments in a matrix organization Over 799 million! - that's how many lives we reached with our products in 2021. And while we are proud of this, we continuously ask ourselves the question: how can we improve and extend even more lives in a world of digital and technological change? We are convinced that we can find answers if curious, courageous and team-oriented people are encouraged to question the status quo, make courageous decisions and follow innovative paths. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 349014BR Sep 29, 2022 Switzerland Job Description 766 million! That's how many patients' lives were touched by our products in 2021. At Novartis, we are reimagining medicine to improve and extend people's lives. We use innovative science and technology to address some of society's most challenging healthcare issues. We discover and develop breakthrough treatments and find new ways to deliver them to as many people as possible. How can we continue to advance our science to help even more patients in need? We believe the answers are found when curious, courageous, and collaborative people are empowered to ask new questions, make bolder decisions, and take smarter risks. In our NTO division we are looking for an experienced QC Scientist (Bioanalytics) who will, under minimal direction, direct and assist in functions supporting QC Bioanalytics. Major accountabilities: • Plan, perform and review Bio-Analytical testing such as Flow Cytometry, ELISA, cell count, cell viability, residual bead assessment, qPCR, Potency, in collaboration with team members, if necessary. • Perform all testing and activities compliantly following appropriate SOPs and procedures. • Work on shifts covering daytime / evening and one or both weekend days. • Contributes to the setup and optimization (LEAN / 6S) of infrastructure or specialized facilities e.g. cell culture or qPCR labs as an expert w/ adequate guidance. • Execute validation/transfers/optimization of test methods as per appropriate protocols. • Execute OOS/OOE and deviation investigations. • Support tracking and trending systems, and programs which assist in the testing, evaluation and monitoring of quality and efficiency. • Generate/revise protocols/reports, SOPs, forms, laboratory data sheets (LDS). Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements - BA or MS in biology, chemistry, biochemistry, microbiology or other related science - 3-8 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture or beneficially within Cell and Gene therapies - Strong knowledge of cGMP and GLP - Thorough Knowledge of Bioassays (FACS, Potency by ELISA) in frame of Cell and Gene therapies - Knowledge of Labware LIMS system - Ability to communicate clearly with a variety of individuals in various aspects of Novartis operations - Detail-oriented with expertise in problem solving and solid decision making abilities - Strong written and verbal communication skills are essential - Fluent in English (written and oral) and understanding German Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Novartis Technical Operations Business Unit NTO QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 352826BR Feb 16, 2023 Switzerland Job Description 10 ! days - that is how long we in Cell & Gene Therapy treat a patient’s T-cells, before returning them with the potential to save a patient’s life. This is a unique and novel personalized treatment where we work with the patient’s own cells during our production process. Not only are we reimagining medicine but we are also impacting on, saving and improving quality of lives, You will play an important part in this as a QA Specialist CGT being a member of the QA Operations Team which is responsible for the overall quality oversight of the production and other operational units within Stein C&GT manufacturing, e.g. Quality Control (QC). The team ensures that the quality strategy is implemented and that there is a continuous drive to improve product and process quality within the operational units. Core activities of the team QA Operations includes: • QA oversight of the production/shopfloor and QC laboratories • Approval of manufacturing deviations • Approval of analytical deviations and OOS/OOE records • Support of QA release of the final product Responsibilities include: • Independent, flexible processing of activities supporting the release of analytical results of raw materials, media, apheresis and finished product (e.g. CoA signature, Batch record review, CoC, Max Dose review...) • Manage OOS/OOE records, SSFs, Deviations, CAPAs in a reliable and efficient manner. Provide ad hoc decisions and act as advisor in day-to-day operations • Manage Exceptional Provisions • Independent, flexible processing of all activities related to the Aseptic Operator Qualification (AOQ) and Aseptic Process Validation (APV), provide guidance on quality questions • Ensures feasible and beneficial monitoring of processes and product related KQIs, and identifies room for improvement. • General Quality Oversight and Review/Approval of Lab Documents/Journals/Lot and release documentation. This includes raw materials/starting materials, vector, apheresis, IPCs, QC samples and finished product • Author/Reviewer/Approver of SOPs/WPs/FRMs. • Audit and Inspection support Pls note: we are offering a temporary Novartis contract, 2 years in duration. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Bachelor of Science in Biology, Biochemistry, Microbiology or related (or equivalent). • Good understanding of cGMP • Fluent English, German skills desired, strong written and verbal communication skills • 3+ years of experiences in pharmaceutical QA, QC, MS&T or production environment • IT-Knowledge (MS Office, SAP, Trackwise, MES) • Ability to communicate clearly with a variety of individuals across different departments in a matrix organization Over 799 million! - that's how many lives we reached with our products in 2021. And while we are proud of this, we continuously ask ourselves the question: how can we improve and extend even more lives in a world of digital and technological change? We are convinced that we can find answers if curious, courageous and team-oriented people are encouraged to question the status quo, make courageous decisions and follow innovative paths. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 363264BR Mar 17, 2023 Switzerland Job Description With 64 manufacturing sites in 26 countries , our aspiration is to become the top manufacturer of innovative and generic medicines in the industry. Your key responsibilities: • Ensure the correct execution of all maintenance activities on HVAC & Clean Utilities equipment. • Preparing the investment and maintenance budget - Responsible for compliance with quality, costs and deadlines. • Managing and coordinating external service providers and suppliers. • Accompanying inspections by authorities (FDA, EMEA, etc.). • Support and implementation of investment and maintenance projects according to budget. • Develop technical solutions for energy savings and plant optimisation. • Identify GMP issues and implement safety and environmental guidelines in plant-related solutions. • Carry out safety and GMP risk analyses. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • 3-5 years of experience in Pharma/Manufacturing sector Engineer (HVAC, Mechanical, or experience in this field) • Fluency in English and German language. • Capability of managing performance improvement and business continuity. • Having a business mindset and stakeholder engagement skills. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Network: Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit SITE DEVELOPMENT Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 367143BR Mar 22, 2023 Switzerland Job Description As Head of Technical Services & Facility Mgt - you will act as touchpoint for maintaining technical excellence for all site stakeholders by understanding their business needs and help drive value, efficiency and quality. What you will do? • Lead the departments HVAC & Clean Utilities, Technical Services and Real Estate Facility Management with direct Leadership responsibility • Lead a strategic and operation department responsible for all buildings on campus Stein and related infrastructure to supports the strategy regarding the Life Science park set up • Be an active member of the Leadership team, balance priorities between various customers, drives assigned initiatives and projects also outside of the own area of responsibility• Ensure compliant authority management well aligned with Quality & HSE • Drive process harmonization and flexibility across the different platforms to enable efficient work • Develop long-term business strategies for buildings and land together with the Business Development department for all Facility services to all partners on site Stein in collaborate with all on site tenants (Novartis internal and external partners) • Anticipate Stein customer needs and/or implications arising from business change taking place at the global or regional level and takes a strategic view when discussing potential solutions with the customer ensuring close collaboration with regions • Ensure safety environment and GxP compliance in the daily operations to ensure requirements of partners, increase safety awareness of employees • Ensure availability of risk management and mitigation plan and providing necessary inputs for Business Continuity and Engineering department • Drive and support cost savings initiatives for the scope of the department in collaboration with the local and global team • Manage and control budgets and expenses of the unit by driving and leading improvement projects gaining effectiveness and superior results • Translate the regional/divisional strategy into a level strategic account plans, provide leadership and sets clear objectives for the campus in line with regional objectives Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring? • 3-5years experience in Pharma/Manufacturing sector • Bachelor Degree in Engineering or equivalent • Technical knowledge of Pharmaceutical/ and equipment qualification, especially HVAC & Clean Utilities • Deep knowledge of GxP requirements for HVAC & Clean Utilities • Ability to represent the organization during Health Authorities and hold the oversight • Ability to work and lead (a cross-functional team) in a matrix environment Team management experience is preferred • Able to understand changing dynamics of Pharmaceutical industry • Proficiency in German & English 743 million! the total no of patients we reached in 2022 through our collective efforts to reimagine medicine and make a real difference to the lives of patients around the world. And while we are proud of this, we continuously ask ourselves the question: how can we improve and extend even more lives in a world of digital and technological change? We are convinced that we can find answers if curious, courageous and team-oriented people are encouraged to question the status quo, make courageous decisions and follow innovative paths.Division Novartis Technical Operations Business Unit SITE DEVELOPMENT Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 362791BR Feb 15, 2023 Switzerland Job Description Through the partnership with more than 1000 external suppliers, our network of 7 technology platforms providesour customers and patientsin more than 150 countries with innovative, high-quality and affordable products –ontime, every time, safely & efficiently. A Senior Process Expert acts as a Subject Matter Expert for all process-specific issues to production within one or more production steps, as well as Launches and Audits, to ensure execution of processes on-time, continuously improving in quality and productivity, performed in compliance to cGMPs, SOPs and applicable guidelines and functional standards (e.g. HSE, NOSSCE). Your key responsibilities: Your responsibilities include, but are not limited to: • Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements. • Responsible for maintaining the master manufacturing documents of assigned products (e.g. Master Batch Record, Bill of Material (BOM) & Recipe, Quality Risk Assessment, Zurich Hazard Analysis) • Ensure that all critical parameters are within written Instruction (i.e. Master Batch Record, Quality Risk Assessment, Validation Protocol). • Support the execution of process validations, and short-term improvement projects, liaising with all the relevant parties at shop floor to ensure accurate execution. • Responsible for creating the master manufacturing documents of assigned products, as appropriate. • Ensure that technical batches generate sufficient process knowledge by thoroughly testing critical variables. • Provides the necessary training and support to new associates joining this position. • Maintain their processes at inspection readiness level and to provide the necessary support in any internal or external audit. This is a temporary position limited to max. 2 years. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • BSc. in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy or equivalent scientific degree. • Desirable MSc. or equivalent experience. • Fluent in English and site local language. • Minimum 5-7 years of experience in process support role on the shopfloor of GMP manufacturing and/or QA/QC. • Proven process understanding (Pharma, GMP, Regulatory aspects). You’ll receive: Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, Unlimited learning and development opportunities. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve. Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 367602BR Mar 15, 2023 Switzerland Job Description 365 days a year, our global manufacturing and supply network works to ensure our patients have the treatments they need to live longer, healthier lives. Preferred start date: 01.Mai 2023 Latest start date: 01.Juni 2023 Duration: min 6 months with possibility to prolong Your responsibilities: - Support to conduct the workplace health risk analyses (ABA), as well as preparation of required documentation, - perform the occupational hygiene measurements e.g. noise measurements, breathing zone measurements of active substances, room climate measurements, - support internal safety and health related programs as well as general HSE topics, such hearing conservation program, respiratory program, personal protective equipment - Administrative and organizational support over HSE audits and inspections Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: - Student or recently completed Bachelor degree / post-diploma in the pharmaceutical or natural scientific field B.Sc., M.Sc., phD. - Specialization in health, safety and environmental sciences; Industrial hygiene is an advantage, - Ability to work in a team, open communication, - Excellent knowledge of German and good English - Very good general computer skills (especially Microsoft Word & Excel) Why Novartis? 236 million. That’s how many lives our products touched in 2022, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Novartis Technical Operations Business Unit SITE DEVELOPMENT Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 362242BR Feb 14, 2023 Switzerland Job Description 150! Unser Werk Novartis Stein ist einer der wichtigsten Standorte für innovative, hochqualitative Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Um Novartis Technical Operations zu verstärken, suchen wir derzeit eine(n) QC Analyst II. Zu Ihren Hauptaufgaben gehören: • Organisation, Durchführung, Auswertung und Dokumentation von mikrobiologischen Routine- Bioburden- und Sterilitätstests von sterilen Produkten unter Einhaltung der GMP-Regeln, QMs, SOPs und GSU- Vorschriften. • Organisation, Durchführung, Auswertung und Dokumentation routinemässiger Methodenvalidierungen sowie laborspezifischer Validierungen • Instandhaltung des Laborbereiches nach 5/6S. • Pflege und Betrieb der Geräte und Einrichtungen, Überwachung des Instandhaltungsprogrammes und der Apparatedokumentation (Logbuch) sowie Durchführung von ad-hoc Aufgaben, die das Fachgebiet betreffen. • Mithilfe bei der Vorbereitung von Behörden- und Kundeninspektionen und Aufrechterhaltung des Informationsflusses innerhalb des Teams. • Einarbeitung neuer Mitarbeiter, Betreuung von Besuchern und Praktikanten sowie Mithilfe bei der Ausbildung von Lernenden oder Produktionsmitarbeiter. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Mindestanforderungen Was ist notwendig für diese Funktion: • Abgeschlossene Lehre als Laborant/in oder äquivalente Ausbildung. • Erfahrung in der Pharmaindustrie (Qualitätssicherung, Produktion steriler Formen) • Erfahrung in mikrobiologischer Analytik • Deutsch: fliessend (mündlich/schriftlich) • Englisch: Grundkenntnisse Wünschenswerte Anforderungen: • Gute Computerkenntnisse (MS Office etc.) • Hohes Maß an Selbstständigkeit und Organisationsfähigkeit Warum Novartis? 799 Millionen! - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden gegebenenfalls im Vorstellungsgespräch besprochen. Werden Sie Mitglied in unserem Novartis Netzwerk: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 361617BR Feb 14, 2023 Switzerland Job Description 350000! Die Anzahl an Umgebungskontrollmustern pro Jahr, die in unseren Laboren analysiert werden. Das Monitoring Team besteht aus 25-30 Mitarbeitern. Wir benötigen Verstärkung innerhalb des QC EM Labors, welches für die Analyse von Umgebungskontrollmustern für den Bereich CGT und das Rheingebiet (Basler Sites) zuständig ist.. Aufgabenbereich: •Organisation, Durchführung, Auswertung und Dokumentation der mikrobiologischen Umgebungskontrollen (Luftkeimzahlbestimmungen, Oberflächenkeimzahl-Bestimmungen und Desinfektionsmittel) für Stein und fürs Rheintal unter Einhaltung der GMP - Regeln, QMs, SOPs und GSU- Vorschriften. •Eingabe der Resultate ins SAP / QC Micro Datenbank, ggf. Auslösen von Deviations, Erstellung von Trendberichten, sowie Archivierung der Dokumente. •Erstellen und Pflegen der QC Micro Datenbank und Auslösen von Aufträgen. •Organisation, Durchführung, Auswertung und Dokumentation des Environmental Monitorings on Surprise •Auswertung und Dokumentation von Reinigungs- und Raumvalidierungen. •Mithilfe bei Abklärungen von OOS-Resultaten und Deviations •Instandhaltung des Laborbereiches nach 6S. Pflege und Betrieb der Geräte und Einrichtungen. Überwachung des Instandhaltungsprogrammes und der Apparatedokumentation (Logbuch). •Mithilfe bei der Vorbereitung von Behörden- und Kundeninspektionen und Aufrechterhaltung des Informationsflusses innerhalb des Teams. Einarbeitung neuer Mitarbeiter, Betreuung von Besuchern und Praktikanten. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Zu Ihren Aufgaben gehören unter anderem: • Bereitschaft in einem 7-Tage Schichtmodell zu arbeiten • Erfahrung in Analysen von Umgebungskontrollmustern und/oder aseptischem Arbeiten • Erfahrung im GxP Umfeld und in Datenintegrität • Gute Planungs- und Koordinationsfähigkeit • Gute Kommunikationsfähigkeit in Deutsch und Englisch • Wünschenswert sind Erfahrung im Abweichungsmanagement und elektronsicher Datenaufnahme im SAP Warum Novartis? 799 Millionen! - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden gegebenenfalls im Vorstellungsgespräch besprochen. Werden Sie Mitglied in unserem Novartis Netzwerk: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Regular Shift Work Yes Apply to JobAccess Job Account

Job ID 365013BR Mar 12, 2023 Switzerland Job Description 150! Unser Werk Novartis Stein Steriles ist einer der wichtigsten Standorte für innovative, hochqualitative, sterile Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Unser Werk Novartis Stein Steriles ist einer der wichtigsten Standorte für innovative, hochqualitative, sterile Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Um die Abteilung Novartis Technical Operations zu verstärken, suchen wir per sofort 1 Prozessmitarbeiter(-in) im Bereich der Flüssigvialabfüllung (Isolatortechnologie) mit Schichtbereitschaft (inkl. Nachtschicht). Zu Ihren Aufgaben gehören unter anderem: • Abfüllung der hergestellten Produktlösung in der korrekten Menge und unter Einhaltung aseptischer Bedingungen • Bedienung der Fertigspritzen Füllmaschine sowie weitere Anlagen (z.B. e-Beam, Isolator, Autoklaven) • Zone – A Eingriffe im Isolator inkl. Mikrobiologisches Umgebungsmonitoring • Isolator Vorbereitung für Produktion und Integritätsprüfungen von Belüftungs- /und Produktfiltern • Reinigungen und Desinfektionen aller Art (Anlagen, Kleinteilen und Umgebung) sowie Durchführen von CIP (Cleaning in Place) und SIP (Sterilizing in Place) • Unterstützung des Technischen Supports bei Fehlerbehebung und Formatwechsel der Anlage • cGMP Dokumentation der durchgeführten Prozesse und Kontrolle der Produktionsprotokolle • Autonomes Planen, Organisieren und Durchzuführen von Prozessen unter Einhaltung vom Produktionsplan im Schichtbetrieb Dies ist eine befristete Stelle für 2 Jahre. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie mitbringen werden: • Einige Jahre Berufserfahrung in der Biotechproduktion von Vorteil • Erfahrung in der Bedienung von Anlagen (e.g. CIP/SIP, Isolator und FVA - Füllverschliessanlage) • Abgeschlossene Berufslehre als Chemie- und Pharmatechnologe oder ähnliches oder langjährige, einschlägige Berufserfahrung in der Chemie- oder Pharmabranche • Technisches Verständnis, Erfahrung in GMP Umgebung, zügiges und eigenständiges erlangen von Kenntnissen über die relevanten SOP's und Vorschriften (z.B. Anlage-spezifische SOP's, Ansatzspezifische SOPs, Hygienekonzept, GSU-Vorschriften, etc.). • Sehr gute Deutschkenntnisse in Wort und Schrift. Englischkenntnisse sind gewünscht. • Motivation, Flexibilität und Team Fähigkeit • Affinität für digitale Technologien (MES/PAS-X Erfahrung) • SAP Erfahrung von Vorteil • Train-The-Trainer Ausbildung von Vorteil Warum Novartis? 799 Millionen! - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden gegebenenfalls im Vorstellungsgespräch besprochen. Werden Sie Mitglied in unserem Novartis Netzwerk: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit LARGE MOLECULES Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 363408BR Feb 13, 2023 Switzerland Job Description 28.000 Mitarbeiter aus mehr als 100 Ländern! Diese Stelle beinhaltet die rechtzeitige Bereitstellung von Materialien für Batch Processing in Cell & Gene Therapies Stein in der richtigen Menge und Qualität, sowie Versand von Finished Product, Einlagerung und Auslagerung sowie die dazugehörigen Buchungen im SAP. Diese Stelle ist auf maximal 2 Jahre befristet. Ihre Haupttätigkeiten: • Annahme von Warenlieferungen für Cell & Gene Therapies, insbesondere von biologisch gefährlichen Materialien • Einbuchung von Materialien in SAP • Einlagerung von eingehenden Materialien gemäss den GMP- und HSE-Anforderungen • Handhabung von Tiefkühltransportbehältern mit Flüssigstickstoff bei Annahme und Versand von menschlichen Zellen • Festgestellte Abweichungen beurteilen und mit Vorgesetztem weiteres Vorgehen besprechen • Bereitstellung und Verwendung von korrekten und geprüften Einsatzkomponenten • Sicherstellen einer termingerechten Abarbeitung der anfallenden Aufträge, Priorisieren von Massnahmen zur Auflösung von Rückständen • Abstimmung der PU internen Ziele mit globalen Anforderungen; Kommunikation mit der Produktionsplanung und der PU Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie zur Rolle mitbringen: • Abgeschlossene technische und/oder kaufmännische Ausbildung/Berufslehre • Berufserfahrung in der pharmazeutischen Produktion, Produktionsplanung oder Logistik • Sicherer Umgang mit SAP und MS-Office Anwendungen • Deutsch in Wort und Schrift sehr gut • Englisch in Wort und Schrift min. Grundkenntnisse Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Engagement für Vielfalt & Inklusion Novartis ist bestrebt, ein hervorragendes, integratives Arbeitsumfeld und ein vielfältiges Team aufzubauen, das die Patienten und Gemeinschaften, denen wir dienen, repräsentiert. Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 365767BR Feb 27, 2023 Switzerland Job Description 743 million! the total no of patients we reached in 2022 through our collective efforts to reimagine medicine and make a real difference to the lives of patients around the world. As a Technical/ Asceptic Trainer in Cell & Gene Therapy you will deliver technical training and assessed learning outcomes. You may also design and develop learning interventions as well as lead training audit response for site. What more you will do: Training delivery and outcome assessment: · Qualifies associates for technical tasks, following assessment against defined criteria · Delivers engaging technical training programs, using multiple delivery methodologies (OJT, Classroom, virtual classroom etc.) to support qualification of associates to perform technical tasks and develop technical capabilities · Collaborates with T&L Operations Experts (in GOC) on logistics for live training, including room booking, LMS entry, material preparation etc. · Supports T&L in GOC in definition of local training plans · Monitors learning effectiveness and outcomes in line with expected business performance, continuously improves technical training Training design and development: · Performs thorough training needs analyses, to ensure that learning outcomes match business needs · Design and develop technical training programs, aligned with the site strategy and local training plans · Ensures development of appropriate evaluation methods to assess learning outcomes · Where relevant, supports the transfer of technical training programs to other trainers and other locations Audit and Inspection Response: · Present site training strategy and respond to auditor questions · Support GOCs in audit preparation and response · Lead any corrective actions which are implemented on site HSE & Quality: · Ensure all activities in compliance with cGxP, incl. data integrity · Comply with all HSE guidelines · Detect and report potential accident, risks and propose solutions · Responsible for participating in initial training and retraining Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Job Sourcing Statement You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV. Minimum Requirements What you will bring: Relevant Experience · 5+ years in production in the Pharmaceutical industry, preferably including many involved functions. · Experience and qualification in instructional design, adult learning principles and learning effectiveness evaluation methodologies an advantage Education & Qualification · BSc in Life Sciences, Behavioral or Educational Sciences, or equivalent. Demonstrated experience in Training and Learning advantageous Languages Advanced level in English and proficient in German.Division Novartis Technical Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma Basel Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 363518BR Feb 13, 2023 Switzerland Job Description 28,000 associates of more than 100 nationalities! Deliver high quality and affordable medicine on time, every time, safely and efficiently. Be part of an important QA Group releasing products with high quality and take opportunity to learn the responsibilities of a QA function. This position is limited until 31st of December 2023. Your key responsibilities: • Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity & eCompliance • Support exception investigations • Review & approval of production, QC, and AS and T records • MBR review • Support OpEx improvement projects Qualified Person • Executes batch release in compliance with registration • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt • Distribution of marketing samples (where applicable) Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Bachelor in science or at least 3 to 5 years in manufacturing or laboratory are with respective apprenticeship • 3-5years experience in Pharma/Manufacturing sector in analytical lab in a GMP environment/equivalent Expertise in GxP operations Able to understand changing dynamics of Pharmaceutical industry • Fluent in English and German • Knowledge in aseptic processing/sterile manufacturing or laboratory environment • Knowledge in GMP, good documentation practice, eCompliance and Data Integrity You’ll receive: Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, Unlimited learning and development opportunities. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve. Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 364345BR Mar 07, 2023 Switzerland Job Description 28.000 Mitarbeiter aus mehr als 100 Ländern! Liefern Sie qualitativ hochwertige und erschwingliche Medikamente pünktlich, jederzeit, sicher und effizient. Ihre Haupttätigkeiten: • Visuelle Überprüfung von AQL-Mustern, Freigabemustern der QC und Rückstellmustern sowie die Interpretation der Ergebnisse (AQL-Limite, Release Spezifikationen,..) • QA-Rundgänge und QA-Oversight auf dem Shopflor • Reinigungen aller Art (Anlagen und Bodenreinigung) • Ausfüllen der Herstellpapiere und Pflege der Logbücher, Ausfüllen der PAS und Losdokumentation • PMX Eingabe / Aufträge starten und beenden / Buchungen vornehmen • Absprachen beim Produktionsplan mit den Kollegen der Optischen Kontrolle, Organisierung des Durcharbeitens der Pausen je nach Situation Dies ist eine befristete Stelle mit dem Ablaufsdatum 31.12.2023. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie zur Rolle mitbringen: • Schulabschluss / abgeschlossene Berufslehre; gute GMP-Kenntnisse, EDV-Kenntnisse (MS Office Paket; SAP, 1QEM), Kenntnisse der Abläufe innerhalb Novartis Steriles von Vorteil • Sehr gute Deutschkenntnisse • Erfahrung in der pharmazeutischen Qualitiätskontrolle, Qualitätssicherung oder pharmazeutischer Produktion. • In der Lage sein, einzelne, spezifische Aufgaben im Bereich Freigabe anfallende Tätigkeiten selbstständig zu bearbeiten • Fähigkeit im Team zu arbeiten, eine gepflegte Feedbackkultur besitzen • Leben der Stopp-Kultur Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Novartis Technical Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Part Time Part Time percentage 50 Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 362955BR Mar 17, 2023 Switzerland Job Description > 150! That’s how many countries we deliver our ampules, pre-filled syringes, vials and auto injectors to. Take part in this achievement by joining our manufacturing teams at Novartis Stein! This Process Expert Postgraduate internship is a position limited to 1 year and is a great opportunity to see how we are making medicine and what kind of challenges we have to overcome in order to bring drugs to the market on time. You will help the Manufacturing Unit packaging Steriles to improve processes and to support the team in processing deviation reports. You will be integrated in a great team and will learn assembly and packaging processes from autoinjectors, Safety Devices, Vials and ampules. Preferred start date: as soon as possible Duration: 1 year (Option for prolongation may be possible) Your responsibilities will include: • Provide front line scientific expert support for all process-specific issues to ensure execution of processes on-time; in compliance to cGMPs, SOPs and applicable guidelines and functional standards (e.g. HSE, NOSSCE) and to allow continuously improving in quality, productivity efficiency • Processing of process deviations and market complaints • Writing of Standard operational procedures (SOP) • Responsible for creating and maintaining the master manufacturing documents of assigned products #LI-Onsite Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Education: Bachelor or Master degree in Pharmacy or Pharmaceutical engineering, Chemical Analytics or Technical engineering profile (degree completed within the past ca. 12 months) • Languages: good German and good English necessary • Experience/Professional requirements: - Expertise with / Knowledge of GMP - Good technical understanding, process management understanding - Knowledge of MS-Office applications - Soft Skills: ability to understand complex issues, analytical thinking, good communication skills, conflict management, action-oriented, resilient, team player with strong team spirit Please submit a cover letter that includes your motivation for the position and from when you will be available. Thank you. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis!Division Novartis Technical Operations Business Unit LARGE MOLECULES Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 365545BR Feb 27, 2023 Switzerland Job Description What you will do as a Shiftlead in CGT: 1. Leadership and people management: · Represent production management to the team members and promote Novartis values within the team · Line responsibility and shift walkthrough · Engage and motivate the team and delivers strong results with an empowered team · Actively participate to the talent agenda: Leads people processes through recruitment, training, coaching and performance to meet all operation requirements sustaining manufacturing unit competitiveness and diversity. 2. Coordination and problem solving · Translate operational schedule into team activities and optimize the use of technical resources to reach daily goals. 3. Quality · Promote and improve the Quality culture. 4. HSE · Promote and improve the HSE culture, by implementing the necessary systems and actions in line with the evolution of the site. 5. Continuous improvement · Manage the process of continuous improvement at the workshop level by fostering innovation and initiatives through actions on shop floor. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Job Sourcing Statement You are applying to be part of the Novartis Talent Pool. We are not currently recruiting for this role but we are building a pipeline for future opportunities. If you would like to be considered for a similar position in future, then please submit your CV. Minimum Requirements What you will bring: · Minimum 5 year experience in chemistry / food / pharmaceuticals / biotech / aseptic manufacturing or development + Min. 2 year experience in a coordination role in GMP environment Education & Qualification · Technical education is required; University degree in Science is desirable, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent job experience Languages: Intermediate English/ Proficiency in German. Competencies: · Team player with good leadership skills · Objective Setting and Performance Management, Lean Management · Change management, adaptability, ability to work under pressure · Quality & Safety Focus · Good working knowledge of manufacturing execution systems (Delta V, MES, SAP, or other as applicable)Division Novartis Technical Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma Stein Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 362898BR Jan 26, 2023 USA Job Description 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, there is more we can do to help improve and extend people’s lives. In Global Regulatory Affairs CMC, our work starts when a compound goes into clinical trials. Novartis has a unique and promising portfolio. All of these innovative projects are aimed at making a difference in patients’ lives and we need your help. As a senior member of our Global Regulatory Affairs CMC team, your role would be to establish and drive global CMC regulatory strategic and operational direction and documentation for complex projects and products covering development, registration and approval/post approval activities. Your Responsibilities include but are not limited to: • Formulate, lead and drive global CMC regulatory strategy across all therapeutic areas and technology platforms, support projects/products drawing on extensive regulatory expertise with a focus on innovation, improving the business benefit equitable with regulatory risks and compliance • Lead and drive all global CMC submission activities (planning, authoring, reviewing, coordination, submission) for assigned projects/products, while applying the global strategy into submissions • Identify the required documentation and any content, quality and/or timeliness issues for global submissions and negotiate the delivery of approved technical source documents in accordance with project timelines • Author and/or review high-quality CMC documentation for Health Authority submissions, establishing and applying CMC global regulatory strategies, current regulatory trends and guidelines. Ensure technical congruency and regulatory compliance, meeting agreed upon timelines and e-publishing requirements • Represent Global Regulatory CMC on cross-functional project teams and maintain collaborative partnerships with stakeholders • Initiate and lead Health Authority interactions and negotiations including more complex interactions; setting objectives, preparing briefing books, coordinating and planning rehearsals and risk mitigation plans. Establish and maintain a single point of contact with FDA • Act as a role model, providing strategic advice within and outside of RA CMC, driving continuous improvement and building the talent within the team through coaching and mentoring Diversity & Inclusion / EEO The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Minimum Requirements What You’ll Bring to the Role: • Education Minimum: Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent; advanced degree desired • Minimum 10 years regulatory experience preferred and/or pharmaceutical industry experience • Experience with mRNA/siRNA technology platforms is a plus • Extensive knowledge/experience in regulatory submission and approval processes and ability to solve complex CMC regulatory issues and requirements • Proven ability to critically evaluate data from a broad range of scientific subject areas • Demonstrated track record to successfully lead/work in interdisciplinary global teams; leading, planning, and prioritizing activities simultaneously on multiple projects • Demonstrated ability for innovative and big picture thinking • Strong planning, negotiation, organizational and interpersonal skills • Excellent written/spoken communication, and negotiation skills Why Consider Novartis? In this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to take smart risks. We are Novartis. Join us and help us reimagine medicine. Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. The pay range for this position at commencement of employment is expected to be between $183,200 and $274,800/year; however, while salary ranges are effective from 1/1/22 through 12/31/22, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit REG AFFAIRS GDD Location USA Site East Hanover, NJ Company / Legal Entity Novartis Pharmaceuticals Alternative Location 1 Switzerland Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 359719BR Dec 07, 2022 USA Job Description Why Novartis? 766 million. That’s how many lives our products touched in 2021 and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to tackle the world’s Reporting to the CEO, the Corporate Strategy team drive high profile, company-wide strategic initiatives that address the top priorities for the company whilst supporting the five core pillars of our Strategy: Unleash the power of our people; Deliver transformative innovations; Embrace operational excellence; Go big on Data & Digital and Return more to society. While our roles are highly visible and demanding, we have a unique opportunity to shape global healthcare trends and work with senior leaders across our businesses to execute our company’s agenda. Your responsibilities include, but are not limited to: •Independently drives strategic business projects for Novartis Group, the CEO and the Executive Committee •Generates strategic insights based on best-in-class analysis, distills outputs and recommendations which enable informed decisions of top-level leaders •Actively contribute to annual strategic planning process •Invests in knowledge / functional spike on behalf of strategy team •Proactively identifies trends and opportunities to shape the CEO and ECN agenda •Provide insight into Health Care Systems as our core customer •Develop network of functional experts and strategy managers across Novartis Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion, or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network We are Novartis. Join us and help us reimagine medicine. Diversity & Inclusion / EEO The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Minimum Requirements MD, PhD or MBA from a top business school preferred or equivalent on-the-job experience •High proficiency in English •Deep knowledge of the Pharma industry •At least 4-5 years of consulting experience at a top tier consultancy (engagement manager or associate principal level) •Extensive project and program management experience in strategic projects •Track record of strong business impact The pay range for this position at commencement of employment is expected to be between $183,200 to $274,800/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factorsDivision ONCOLOGY Business Unit ONCOLOGY BU Location USA Site Cambridge, MA Company / Legal Entity Novartis Corporation Alternative Location 1 Switzerland Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 357871BR Nov 11, 2022 USA Job Description 1,800+ associates. 86 countries. One Regulatory Affairs. At Novartis your voice, experience, and quality mindset can truly make a difference in Regulatory Affairs (RA). Novartis has a unique and promising portfolio with 70 projects as potential NMEs in development, 65 projects in Phase 3 or already undergoing registration, and 100 Phase 1/2 projects. We also focus on rare disease areas; in fact, more than 80% of our innovation is targeted on areas of high unmet need. In many cases, we can offer family friendly work flexibility to facilitate your physical and mental health. Read on to learn about the role available in Regulatory Affairs. We hope you will consider joining our global OneRA family. The RA Senior Global Labeling Manager (Sr. GLM) is responsible for the creation and maintenance of regulatory compliant, competitive, and up-to-date core labeling documents for assigned developmental programs and Novartis Innovative Medicines products. The assigned products should be of higher complexity products and may include developmental programs. The RA Sr. GLM provides strategic and operational regulatory labeling input and works in close collaboration with Expert Labeling Task Force (ELTF) members in creating or maintaining core labeling documents and handling HA or CO labeling queries for assigned products. Your responsibilities will include but are not limited to: • Serve as the labeling lead for all labeling related topics for Novartis products and development projects • Coordinate and lead the ELTF to discuss labeling strategy and reach consensus on labeling course of action and labeling text as appropriate • Lead and/contribute to presentations on labeling related topics for the assigned products at relevant board/forum/committee (e.g., GLC, SMT, MSRB, PSB) • Contribute to global labeling management and continuous improvement initiatives, review and comment on emerging regulatory labeling guidelines • Represent GL during audits and inspections Diversity & Inclusion / EEO The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Minimum Requirements What you’ll bring to the role: • Science based degree, advanced degree preferred (MD, PhD PharmD) • Extensive experience (at least 4-6 years) in global labeling, alternatively extensive experience (5 + years) in related areas of the pharmaceutical industry or Health Authorities • Experience with new product development and with managing Oncology products • US and EU Labeling filing experience • Strong interpersonal, project management, communication, negotiation and problem-solving skills • Ability to lead cross-functional teams in a matrix environment • Sound understanding of medical and scientific terminologies and good understanding of drug safety information 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to: [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. The pay range for this position at commencement of employment is expected to be between $124,000 and $186,000/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit REG AFFAIRS GDD Location USA Site East Hanover, NJ Company / Legal Entity Novartis Pharmaceuticals Alternative Location 1 Switzerland Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 345801BR Mar 15, 2023 USA Job Description 6000! This is the number of associates in the Novartis Institutes for BioMedical Research (NIBR). This division is the innovation engine of Novartis, focusing on new technologies that have the potential to help produce therapeutic breakthroughs for patients. The Disease Area x (DAx) department is accommodated within NIBR and is a group of about 145 scientists that work in close collaboration with colleagues from Novartis Research and Development on several therapeutic areas with high unmet need, including kidney disease. Using a diverse array of approaches and cutting-edge technology, DAx aims to develop drugs that improve the lives of individuals suffering from chronic kidney diseases for which there is currently no cure. Impact of this position We are seeking an innovative, independent and dynamic renal research scientist with broad expertise in molecular and cellular biology to join a discovery biology team focused on developing innovative therapeutic agents in the area of polycystic kidney disease (PKD). Your key responsibilities Your responsibilities will include, but not limited to: • Contribute to the NIBR drug discovery process with the goal to discover and develop novel therapeutic treatment options for patients with PKD. • Conduct impactful research in the area of PKD and provide scientific leadership and innovation by acting as subject matter expert on genetic cystic kidney diseases. • Lead early drug projects in the renal disease space, propose and champion new targets and novel approaches for disease treatment. Act as a leader of a team tasked with the triage and validation of new biology knowledge harnessed from genome wide and pharmacological screens in complex 3D human model systems. • Design and execute in vitro and in vivo experimental research plans to evaluate targets modulating renal cyst expansion, inflammation and fibrosis. • Develop assays and implement new technologies to enable the delivery of high quality data-driven package and enable project decisions a/o portfolio transitions. Record and interpret experimental data, and present results to project team members. • Engage in interdisciplinary research requiring the application of specialized scientific knowledge and advanced laboratory techniques, in particular engineered complex cellular models and their use with chemical biology and gene editing approaches. • Collaborate with other scientists in a global matrixed dynamic environment fostering innovation and advance project activities. Develop and maintain external relationships/contacts. • Deliver impact to projects by identifying technical trends, both internal and external to your discipline. The pay range for this position at commencement of employment is expected to be between $118,400.00 and $177,600.00 per year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Diversity & Inclusion / EEO The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Minimum Requirements Minimum requirements What you will bring to the role: • A PhD and/or MD degree with postdoctoral experience and a minimum of three years of research in renal biology and physiology, preferably in the pharmaceutical / biotechnology industry or academia. • In-depth knowledge of (patho-)physiology of PKD, including direct experience with PKD mechanisms and complex in vitro renal cell-based platforms recapitulating human cystic phenotype and in vivo models of disease progression. • Extensive “hands-on” experience and proven track-record in the use of a wide range of cellular, biochemical and genome editing methods and technologies to unravel complex cellular signaling pathways • Familiarity with “state of the art” computational and analytical approaches and be comfortable with analyzing large scale datasets • A track record of leading drug discovery projects and working alongside disease areas specialists to bring mechanistic target biology and target validation understanding for renal diseases. • Strong communication skills with an ability to effectively interact with people in a dynamic matrix environment, both internally and externally • A proven scientific impact on innovation through a solid publication track record and strong external scientific network with academic experts. • Excellent oral and written communication skills (in English) are essential Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision NIBR Business Unit CBT - NIBR Location USA Site Cambridge, MA Company / Legal Entity NIBRI Alternative Location 1 Switzerland Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 362457BR Feb 21, 2023 USA Job Description 13! The number of medicines Cardio Renal Metabolic diseases currently in development at Novartis. Novartis is deeply committed to transforming the lives of people living with cardiovascular, renal and metabolic diseases. We believe that anyone living with these conditions has the right to a life free from pain, free from symptoms and free from disease - this is our vision for the future. Our mission is to reimagine medicine to extend and improve people’s lives – and our overall company strategy to achieve this is to Focus Novartis as a leading medicine company powered by data science and advanced therapy platforms The Clinical Development Medical Director (CDMD) is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As CDMD, you will have oversight of the clinical development for the assigned programs and drive execution of the clinical development plan. In addition, you will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. Your responsibilities will include, but are not limited to: • Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program • Leading development of clinical sections of trial and program level regulatory documents • Driving execution the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable • Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues • Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas • As a medical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards • May work with NIBR (Novartis Institute of Biomedical Research/ Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed. Diversity & Inclusion / EEO The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Minimum Requirements What you'll bring to the role: • MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area; Clinical practice experience 4 years (including residency) and board certification or eligibility in oncology or hematology preferred • Minimum of 7 years of experience in clinical research or drug development • Experience in an academic clinical research or industry environment spanning clinical activities in Phases I through IV required. • 2 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry required. • Working knowledge of disease area is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports • Demonstrated ability to establish effective scientific partnerships with key stakeholders • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes • Previous global people management experience is preferred, though this may include management in a matrix environment. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. The pay range for this position at commencement of employment is expected to be between $245,600 and $368,400 annually; however, while salary ranges are effective from 1/1/23 through 12/31/23, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.Division Global Drug Development Business Unit CARDIO-RENAL-METAB GDD Location USA Site East Hanover, NJ Company / Legal Entity Novartis Pharmaceuticals Alternative Location 1 Switzerland Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 365505BR Mar 08, 2023 Switzerland Job Description 1886! Wir haben mehr als 130 Jahre Erfahrung in der Behandlung von Patienten. Sandoz, ein Geschäftsbereich von Novartis, ist ein weltweit führender Anbieter von Generika und Biosimilars, der sich dafür einsetzt, den Zugang zu Medikamenten weltweit zu fördern! Der Medical Sales Representative ist verantwortlich für das Erreichen der Verkaufsziele und die Bewerbung der Produkte bei Apothekern und anderen Health Care Professionals für die zugewiesene Region. Aufgaben • Sachkundige Beratung und Betreuung von Apotheken sowie Ausbau von Kundenpotenzialen • Unterstützt die Entscheidungsfindung von HCPs zur Optimierung von Patientenergebnissen durch die Bereitstellung der relevanten Daten, Schlüsselbotschaften und Krankheitsinformationen • Nutzt alle verfügbaren Datenquellen um Gebiets- und Kundenbindungspläne zu erstellen, adaptieren und priorisieren • Unterhält ein fundiertes und aktuelles Wissen über Industrie, therapeutisches Gebiet, Mitbewerber und Käuferdynamik und konzentriert sich auf prioritäre Kundenchancen • Nutzt Methoden zur Kundenbindung vollumfänglich um qualitativ hochwertige Kundeninteraktionen zu erstellen und damit das Kundenerlebnisses zum Wohle der Patienten zu maximieren • Verhält sich entsprechend ethischen Richtlinien, behördliche Auflagen und Sandoz Werten und Verhaltensweisen • Meldet technische Beschwerden, unerwünschten Ereignissen, Sonderfall-Szenarien im Zusammenhang mit Sandoz-Produkten innerhalb von 24 Stunden nach Erhalt Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Anforderungen: • Deutsch obligatorisch. Französisch von Vorteil • 3-4 Jahre Erfahrung im Verkauf oder Vertrieb, vorzugsweise in der pharmazeutischen Industrie • Erfahrung im Key Account Management wünschenswert • Erfahrung in der Produkteinführung wünschenswert • Etabliertes Netzwerk zur gezielten Kundengruppe (Apotheken) wünschenswert • Hohe Reisebereitschaft innerhalb der zugewiesenen Region • Fahrausweis Klasse B Why Sandoz? 500 million patients were touched by Sandoz generic and biosimilar medicines in 2021 and while we’re proud of this, we know there is more we could do to continue to help pioneer access to medicines for people around the world. How will we do this? We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Sandoz! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Join our Novartis Group Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision SANDOZ Business Unit COMMERCIAL OPS EUROPE SZ Location Switzerland Site Zurich Company / Legal Entity Sandoz Pharmaceuticals AG Functional Area Sales Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account