Novartis AG

Job ID 348260BR Sep 21, 2022 Switzerland Job Description 100% revenue growth, that is our ambition for the Biopharmaceuticals business unit for the next 5 years. To broaden access to affordable biologics for patients, this is our purpose at Sandoz Biopharmaceuticals. Sandoz, a division of Novartis, is a global leader in Generic and Biosimilar medicines. We are committed to building on that leadership to drive access to medicine worldwide and are doubling down to build on our already rich pipeline of 15+ biosimilars. Your Key responsibilities: • Scope, lead and drive strategic cross-functional projects, as defined by the Global Head of Biopharma Strategy Portfolio and BD&L, to successful completion with measurable business impact. • Support the Global Head of Biopharma Strategy Portfolio and BD&L in the design and management of annual Strategic Planning processes in alignment with the office of the Sandoz CEO. • Support the Sandoz Biopharma strategy by ensuring project plans are in line with Senior Management expectations through ongoing communication and engagement with project teams • Prepare and present updates to Senior Management. • Prepare key meetings. Actively drive creation of high-quality strategy documentation and ensure timely submission of slide decks and presentations. • Prepare high-level presentations for Global Head of Biopharma Strategy Portfolio and BD&L. Act as point of contact for Biopharma strategy, prepare executive presentations, and support the office of the Global Sandoz Biopharma office as required 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: • A business and/or science background and degree is required. MD, science PhD or MBA with a focus in consultancy, marketing or equivalent experience is desirable. • English fluent, another International language is beneficial • 5+ years pharma industry expertise required preferably in specialty • Ability to align interests of multiple parties, and to be adaptable in a new and evolving area of the business • Pragmatic approach to complexity, outcome driven mindset • Strong business acumen and strategic thinking to bridge marketing and science • Excellent communication and analytical skills (fluent English) 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! 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 SANDOZ Business Unit BioPharma SZ Location Switzerland Site Basel Company / Legal Entity Sandoz AG Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 352256BR Sep 22, 2022 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 Intelligence Analyst (IA) is responsible for the research and collection of threat in-formation from multiple sources, based on agreed intelligence requirements, and for processing this into timely, clear, accurate and actionable intelligence products with the aim of providing business insights in line with Glob-al Security strategy. The focus of the IA 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. A key component of this role is providing intelligence support to combat pharmaceutical crime and protect patient safety through timely detection and reporting of incidents, create the conditions to bring counterfeiters and illegal traders to justice in order to preserve Novartis reputation, business innovation and productivity. Your responsibilities include, but not limited to: • Produce high quality threat assessments, management briefs, multi-media presentations and other relevant security and awareness products providing business insights in line with Global Security strategy. • Work on assigned priorities and to an agreed plan through the systematic collection, collation, evaluation, interpretation and analysis of information and process this into timely, accurate, and relevant intelligence. • Work closely with the Anti-Falsified Medicines team and play a central role in the team’s intelligence effort against pharmaceutical crime. • Provide proactive analytical support and effectively manage the online monitoring and enforcement program to combat pharmaceutical crime. • Review and triage risk-based lines of enquiry from multiple sources and deliver actionable recommendations to support enforcement action. Effectively manage a network of global vendors to empower Anti-Falsified medicines regional leads with actionable intel. • Assess other emerging security risk and trends, extreme events, political instability, social unrest, demonstrations, and crime, gathered from multiple sources (including media, government and NGO contacts, medical providers, trusted vendors, Novartis). • Develop and maintain excellent working and reciprocal relationships with peer professionals, law enforcement, intelligence and security agencies, regulatory authorities, customs organizations, commercial vendors, and other relevant bodies. • Use data digital skills to conduct root cause analysis of complex investigations, predictive analysis/horizon scanning of global security threats and proficiency in SOCMINT analytical techniques. Create and record ‘corporate memory’ of Global Security intelligence activity. 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 (Bachelor’s/Master’s) in relevant subject • A career intelligence / investigations expert: 10+ years who is considered an expert threat analyst. Proven experience in intelligence work applicable to role is essential: e.g. counter-terrorism/ counter-extremism/ counter-narcotics / product security / illicit trade / criminal investigations /other relevant area. Experience in a Military/law enforcement/customs/security intelligence/commercial intelligence background desirable • Strong practical working knowledge I2/analyst notebook and similar applications. Experience in an international / global environment. • Outstanding written and verbal communications. People, influencing and change management experience essential. Ability to influence at senior executive level. • 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! 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. 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 353783BR Oct 06, 2022 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. We are seeking a motivated Research Scientist To perform cryopreservation, re-vitalization and rederivation of genetically modified mouse lines. You will be involved in Project-based support of initial genetic characterization of newly generated mouse lines, thus contributing to in vivo research in various research areas within the Novartis Institutes for BioMedical Research (NIBR). Your responsibilities will include: • Performing embryo freezing, sperm freezing and in vitro fertilization (IVF) experiments according to established protocols. • Perform surgical embryo transfer according to established protocols • In vivo work including handling and breeding of mice and perform different application techniques • Ensuring accurate documentation and reporting of generated data. • General organization and maintenance of the laboratory infrastructure (e.g. ordering of consumables, ensuring periodic maintenance of laboratory equipment). • Focus on the success of the whole Transgenic Services group, delivering state-of-the-art in vitro / in vivo work and showing willingness to support, with high flexibility, other activities of the unit. • Occasional Weekend duty 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: • Minimum Technical diploma in Biology such as Biological technical assistant or equivalent • Swiss LTK1 training or equivalent (international) • Fluent in English – German is a plus • Three or more years of experience in In Vitro Fertilization, Cryopreservation of sperm and embryos, handling and breeding of small laboratory animals, sampling of animals for health monitoring, diverse injection methods, • Experience with ordering processes and logistics • knowledge in surgical Embryo Transfer and Electroporation of rodents • Working knowledge of mouse model types, transgene structures and strategies (e.g. inducible KO), Mendelian genetics Desirable Requirements • Knowledge in molecular biology preferably in genotyping of transgenic mouse models (including in vivo work) • Theoretical knowledge about the process of generating genetically modified animals Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. 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! 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 CFO 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 350572BR Aug 10, 2022 Switzerland Job Description One purpose... to innovate the science of hit generation using DNA-encoded library technology! The NIBR/Schreiber Scholar program under the leadership of Karin Briner and Stuart Schreiber is offering a 3-year postdoctoral position at Novartis Basel (Switzerland) in a transatlantic multi-disciplinary team. Composed of experts from academia and industry, the team develops novel applications of DNA-encoded library technology aiming at exploring new ways to interact with targets of biological relevance. Apply today to join a vibrant scientific community working at the interface of organic chemistry, molecular biology and data science. Conduct cutting-edge science with subject matter experts and publish in leading journals! Expected start date: Fall 2022 Duration: 3 years Your responsibilities: • DNA-encoded library design and synthesis • Development of new DNA-compatible chemistries • Hit identification and follow-up 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: • PhD in chemistry with solid background in organic synthesis • Experience in chemical biology / molecular biology / data science is a plus • Languages: English is a must • Excellent analytical, communication and organizational skills • Candidates must be able to work independently as well as with interdisciplinary teams • Strong publication record is desirable 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 Global Discovery Chemistry 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 352530BR Sep 26, 2022 Switzerland Job Description 100% revenue growth, that is our ambition in International Region for the next 5 years! With more than 3,000 associates serving patients across 4 continents and 19 time zones we have a truly global impact and unlimited opportunities to help people around the world access high-quality medicine. Sandoz, a division of Novartis, is a global leader in Generic and Biosimilar medicines. Job Purpose: The Head Portfolio, International Region leads product portfolio development across the Region, by identifying and driving strategic portfolio choices, pipeline projects prioritization and successful execution of product pipeline in line with Global and Regional growth strategy. Develops and implements best in class Portfolio selection and execution practices across the Region and cross-functionally. Key Responsibilities: • Drive increase in value of new product pipeline across International Region by identifying and selecting high-value strategic assets, ensuring high-quality evaluation, timely allocation to execution and successful progression of selected pipeline assets through all pipeline execution phases from selection to launch. • Develop mid- (next 3-5 years) and long-term (5-10 years) portfolio strategy with a detailed product / country portfolio execution plan. • Maintain and regularly share with direct manager and other relevant functions an in-depth market intelligence for key markets of the Region with clarity regarding market archetype, regulatory aspects, commercial infrastructure as well as relevant customer insights to facilitate high-quality assessments and decision-making; • Implement and foster culture of in-depth assessments and consistent methodology for portfolio evaluations within the Regional Portfolio and across country Portfolio teams – ensuring portfolio choices are based on in-depth evaluations, key value drivers are identified and aligned to market specifics and customer insights, key assumptions are validated, aligned with relevant stakeholders and well-documented, ensuring consistency in portfolio choices and efficient resource allocation. • Establish robust consistent methodology to evaluate, develop recommendations and define most efficient project execution route – allocation to in-house development (PD) or external partnerships (BD) – maximizing pipeline value, probability to launch successfully and availability of critical resources. • Monitor and facilitate efficient progress of projects in execution and timely escalation to relevant stakeholders to ensure pipeline value maximization. • Close alignment with relevant country, Regional and Global functions, including Commercial, Portfolio, BD, Launch Management, Regulatory, Project Management, IP, Legal and other functions to ensure their continued support in Regional Portfolio strategy execution; • Ensure continued team development, increase in productivity and engagement within the Regional Portfolio team and country Portfolio teams by prioritizing learning and development initiatives, fostering engagement and culture of personal growth, acquisition of new skills, pro-active best practice sharing and accelerating innovation 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, MBA or PhD with background in Finance, Economics, Management, Business Administration or Life Sciences. • 7+ years’ experience in management consulting or pharmaceutical portfolio management. • 5+years’ experience in leading and building high performing teams. • Strong financial modelling and valuations skills and in-depth understanding of main financial valuation methods. • Proven ability to drive and execute global projects in various geographies including one or more of the following countries; Japan, Australia, China, Brazil, Mexico, South Africa, • Fluency in English – required; Spanish, Portuguese or Japanese – desirable. 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!Division SANDOZ Business Unit Commercial OPS SIR SZ Location Switzerland Site Basel Company / Legal Entity Sandoz AG Functional Area Marketing Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 354474BR Oct 04, 2022 Switzerland Job Description Responsibility for the design, implementation, adaptation and governance of Sandoz Benefits, pensions, recognition and health and welfare plans worldwide including global cost and risk management in the area of benefits in general (including also global programs in other areas of benefits and perks). Responsibility for the global center of expertise in the area of benefits & recognition representing the Sandoz benefits function internally and externally. Oversight of Sandoz’ pension funds and management (incl. management of external vendors and insurance companies). Key Responsibilities: • Responsibility for the design, implementation and adaptation of Sandoz benefits principles, strategy and guidelines. • Representing Sandoz during the TSA period in various Boards (e.g. Pension Board (NPB)) overseeing the cost and risk management of Sandoz’ pension and post-retirement employee benefit provision. • Responsible for formal requests for new benefit plans or changes in existing plans based on the Sandoz benefits principles coordinating the submission approval process with the NPB during TSA period and the Sandoz Executive Committee. • Support the business and the HR function regarding M&A projects pre- and post-merger in the area of Benefits & Recognition. • Represent the Sandoz benefits function internally and externally by setting up and maintaining a broad network with responsible P&O and Finance managers, consultants, global benefit associations and other parties involved in the area of international benefit management. Ensure pro-active advice and support is provided as well as training and education to ensure a high ROI of the Benefits offerings. • Business responsibility for negotiations with vendors of global benefit administration platforms and recognition plans, health and welfare insurance contracts (via the global multinational pooling network partners) globally and locally in order to optimize savings potential and service levels. Responsibility for the design and implementation of Recognition programs, International Pension Plan, the International Health Plan the global Business Travel Accident program and the Emergency Travel Assistance program. Responsibility for the oversight (at arm’s length) of the Swiss pension funds Number of associates: 1-3 direct Indirect influencing within complex matrix system in respect of benefits and recognition administration. Financial responsibility: Direct and indirect oversight of assets of the Swiss pension funds and global pension and retirement plan assets. Indirect oversight over worldwide annual pension costs/contributions and health and welfare costs/premiums. Amounts of asset value to be confirmed. Significant cost savings and risk reduction for the global organization through pension conversion projects and global benefit projects optimization. Impact on the organisation (where appropriate): Ensure Rewards & Benefits is considered a trusted partner in M&A deals and successfully participate in DD activities where needed Transformatory impact on employee experience through implementation of Total Rewards administration and communication to ensure a high ROI of the investments in Benefits programs 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 Languages: • Excellent English spoken and written plus exposure to other cultures/languages Experience: o At least 5 years of experience in Pensions Administration & Management and in US benefits management. o At least 8 years of experience in global employee benefits including the US market o Several years of leadership experience in multinational employee benefits, good actuarial knowledge and a combination of Finance and HR experience (ideally in Global Mobility and/or Compensation) of advantage. o Strong leadership and management experience in complex organizations, including: o People Leadership, leading large and/or diverse teams o Global project management leadership experience in P&O and in TT system implementation o Organization Scope, Scale and Complexity o Geographic Scope o Critical Negotiations o Industry/ Business Exposure o Financial management o P&L or unit accountability o Global experience of Rewards M&A including due diligence and integration (ideally including US experience) Competencies & Capabilities: Competency Profile: • Applied Business Insights – Generates, identifies and uses broad ideas and insights based on deep business, market, patient and/or customer understanding to drive innovation • Stakeholder Engagement - Engages, influences, aligns and leads internal and/or external stakeholders • Digital & Technology Savvy – Improves business performance by driving change through innovating, advocating and implementing digital and technology solutions • Continuous Learning - Constantly in search of ways to develop, learn and apply knowledge and expertise to meet current and anticipate future challenges • Vision & purpose (strategy to story) – Develops strategy and translates strategy into a simple, compelling & purposeful vision that inspires and motivates • Managing Change – Quickly adapts to meet shifting demands of different situations and operates effectively during times of uncertainty • Joint Value Creation – Partners with stakeholders to co-create value for Sandoz & external stakeholders • Interpersonal Savvy - Works well with diverse groups of people, handles conflict situations effectively and builds formal and informal relationships • Benefits program design • Consulting • Data AnalyticsDivision SANDOZ Business Unit Global HR SZ Location Switzerland Site Basel Company / Legal Entity Sandoz AG Alternative Location 1 Germany Alternative Location 2 Czech Republic Functional Area Human Resources Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 354507BR Oct 05, 2022 Switzerland Job Description Manage the preparation of material for the Board of Directors / Remuneration Committee. Lead the drafting of annual and ad-hoc publications such as remuneration report, say-on-pay, etc. Contribute to executive rewards program designs, governance, and policies. Key Responsibilities: • Provide material and results for the Remuneration Committee meetings and contribute to the preparation and completion of relevant reports and documents. • Contribute to the strategic planning of delivery and compliance in annual reporting, corpo-rate governance processes, and documents required under ever evolving company law, relevant governance requirements, reporting duties, etc. • Lead the writing and completion of the remuneration report in the annual report and re-lated documents (AGM presentations, say-on-pay, investor presentations, proxy advisor documentation, etc.) • Support the preparation and delivery of the remuneration data to be included and set out in the remuneration report, say-on-pay, the note to the financial statements, and other corporate reports. • Lead the audit reviews related to the remuneration report and other related documents. • Oversee and manage overall Rewards Governance and principles. • Contribute to executive compensation policy design, program design and compensation systems, defining and applying the governance framework, etc. • Analyze compensation systems, programs, processes, data (e.g., executive benchmark-ing, incentive pay-out modelling, etc.). Set out results and recommendations tailored to various audiences. • Lead and/or participate in rewards related projects • Substitute and/or support other Executive Rewards and Equity Rewards related activities as required • Pro-actively seek to simplify and improve the way we work Key Performance Indicators: • Develop strong and robust relationships with SEC members, P&O and Reward leadership team members • Compliance or governance risk management (including audit findings) • Delivery of material and processes on time and with high quality • Accurate, complete, and compliant presentation/material for Remuneration Committee reviews 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 Business / Finance (or equivalent) required • MBA, graduate or post-graduate HR and/or tax specialization a plus • English required, other languages are a plus • 10+ years relevant P&O/Rewards experience, prefer-ably in complex, international organization • Advanced understanding of executive rewards, bene-fits practices in main locations, tax aspects on equity plans and Global Mobility benefits • Strong business acumen • Demonstrated P&O business partner mindset and customer sensitivity • Proven analytical and decision-making skills • Ability to communicate complex data in a simple and easy-to-understand manner • Ability to manage, influence and provide solutions to senior stakeholders that often have conflicting priori-ties • Ability to work across P&O disciplines to help the business find solutions to complex cases • Negotiation skills / Ability to professionally challenge decisions even when interacting with senior executivesDivision SANDOZ Business Unit Global HR SZ Location Switzerland Site Basel Company / Legal Entity Sandoz AG Functional Area Human Resources Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 329239BR Nov 16, 2021 Switzerland Job Description As part of the Neuroscience (NS) and Autoimmunity, Transplantation & Inflammatory Disease (ATI) departments at Novartis, you will help to develop therapies for patients with neurologic or psychiatric disorders, as well as for patients who may benefit from a modulation of the immune system. You will provide medical and scientific leadership and expertise in a role that significantly affects the entire Novartis NS and ATI drug development pipeline. You will drive the success of both early and late stage global programs. You will provide scientific expert assessments and support for in-licensing opportunities, including due diligences. Your responsibilities will include: 1. Translational Medicine / early clinical projects: • Develop high value decision-strategies for the Translational Medicine component of drug development projects from Research to clinical Proof of Concept or Proof of Mechanism in a single or multiple indications, including Parallel Indication Expansion-Proof of Concepts • Develop and implement study protocols for different types of clinical studies (First in Human, Proof of Concept, mechanistic and safety studies), and other documents such as investigators brochures. • Responsible for clinical monitoring and integrated safety data review during and after the live phase of a study • Represent clinical Translational Medicine aspects to Health Authorities and other stakeholders (e.g. payers, patient advocacy groups) • Innovation: Champion and drive new clinical compound characterization opportunities and profiling approaches 2. Translational Medicine (late-stage clinical projects): In collaboration with the respective Translational Medicine Therapeutic Area Head: • Responsible for implementing studies during the Proof of Concept phase by providing medical and scientific leadership and expertise to all line functions on the project team. This may include methodology studies to identify and validate novel endpoints for early decision making in Proof of Concept studies. • Communicate clinical team matters to Global Project Teams, relevant Novartis Institutes of BioMedical Research and Global Drug Development boards, and other Novartis Boards as required. • Evaluate clinical centers and foster communication with crucial collaborating investigators, regulatory authorities, and other stakeholders Matrix people responsibility per project 5-8 cross-functional members from Translational Medicine and other line functions per project team Impact of this role? • Design and implementation of early Clinical Development Plan and studies according to the Integrated Development Plan / Clinical Development Plan / Clinical Pharmacology Plan enabling efficient and rational decision-making, high probability of fast drug registration, favorable drug label and high competitiveness of compounds • This role has a key impact on the entire Novartis pipeline, transitioning programs from preclinical through early clinical and ultimately to full development via the Proof of Concept mechanism, and driving the program after Proof of Concept by delivering key Profiling data to support regulatory submissions • As a recognized specialist in field, drives project team clinical strategy. Works globally across various Novartis Institutes and Divisions as well as country organizations as appropriate 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 will bring to the role: • Medical Degree. PhD/post-doctoral and / or specialized further training (board certification) and / or clinical research experience in Clinical pharmacology. • An expertise in translational medicine applied to neurology and immunology. • Record of drug submissions / approval and / or high quality publications in international scientific journals. • Previous relevant & significant clinical study experience: either from pharma/biotech leading early phase clinical trials; a senior role within a CRO responsible for managing the medical relationship with Sponsors; from a relevant academic medical center with PI & co-PI clinical trial experience. • Business fluent in English (written and spoken)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 352951BR Oct 05, 2022 Switzerland Job Description 6000+! The number of scientists in the Novartis Institutes for BioMedical Research (NIBR). The Musculoskeletal Disease Area (MSD) at the Novartis Institutes for Biomedical Research (NIBR) is investing in the discovery of novel and transformative therapies for ​patients affected by neuromuscular, tendon and cartilage diseases. ​ As part of this effort, MSD is seeking an innovative and highly motivated Principal Scientist to develop, shape and advance novel therapies aimed at prevention and regeneration of neuromuscular, cartilage and tendon diseased tissues. You will be responsible for leading a state-of-the-art laboratory of experienced scientists, employing ground-breaking technologies to explore disease mechanisms and pathways, identify novel targets, mechanistically dissect their function and provide detailed characterization of mechanism of action of novel molecules, to enable progression of the drug discovery pipeline. This will include the use of complex in vitro assays, patient relevant cellular and ex vivo model systems to evaluate innovative therapeutic modalities (small molecules, biologics, gene therapies) with potential for long-term impact on the disease course. As a member of the NIBR community, you will also contribute to and benefit from a highly interdisciplinary and collaborative global community with extensive know how and resources in data sciences, chemistry, biologics, cell and gene therapy as well as chemical biology. Your responsibilities will include • 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 • Identify novel therapeutic targets and biomarkers candidates, establish in vitro tools and assays to progress drug discovery effort, elucidate mode of action of drug candidates, and explore the mechanistic translatability of pre-clinical models. • Design and conduct experiments to address key scientific questions for various project, develop disease-relevant cellular systems with phenotypical and functional readouts using cutting-edge technologies to decipher biology of novel targets • Closely collaborate with scientists, clinicians, and technology experts across different departments in the global organization • Guide, supervise and develop scientific associates • Present concepts and projects in a clear, scientifically sound, and data-driven, objective manner in different settings and venues • Manage lab resources in a flexible manner to adapt to changing priorities 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: • PhD + a minimum of 3-5 years of relevant research experience in an academic setting and/or in the pharmaceutical/biotech sector, ideally with focus in molecular biology, biochemistry, cell biology in musculoskeletal diseases relevant areas • Experience in target identification, validation and working with primary cells, or establishing cellular assays, or extensive cellular signaling experience, with an emphasis on disease pathways would be helpful • Experience in biochemistry, in molecular and cellular biology to decipher the biology of novel targets and at establishing physiologic assays using human or iPS-derived patient cells, with functional or phenotypical readouts • Experience in cutting-edge novel therapeutic approaches (e.g. gene-, RNA/DNA- or cell-therapy, complex biologics modalities, etc) • Significant scientific accomplishments and successful collaborations documented by publications in high-impact journals • Aptitude to work and thrive in cross disciplinary teams, coupled to good organization, communication, presentation and analytical skills. • Proactive and dynamic attitude with a demonstrable inquisitive mindset and a proven ability to formulate, articulate, and critically evaluate data driven scientific hypotheses and build next steps. Outstanding learning agility. Desirable requirements: • In-depth knowledge of complex human culture systems interrogated for regeneration potential. • Experience in translational science, data science and/or biomarkers identification would be a plus. 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. Imagine what you could do 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 MUSCULOSKELETAL - 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 348620BR Jul 27, 2022 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 to join a laboratory that carries out cutting-edge oncology drug discovery pharmacology research. We seek an experienced, motivated and ambitious associate wishing to continue a successful scientific career in a fast-paced drug discovery environment. You will work collaboratively as an active member of lab and global project teams using a wide range of in vivo and in vitro techniques, closely interacting with your lab head and colleagues. You will join the Global Oncology Drug Discovery group contributing to develop novel cancer therapeutics and bring innovative targets into our world leading Oncology portfolio. The position is based at the Novartis Institutes of BioMedical Research (www.nibr.com) in Basel, Switzerland. Responsibilities include but are not limited to: • Design, perform and evaluate experiments to characterize novel drug candidates for oncology projects in various in vitro and ex vivo assays (e.g. cell culture, transfections, proliferation assays, ELISA, PCR, Western blotting, FACS) • Develop and characterize novel innovative in vivo oncology models using molecular imaging techniques • Independently search for information in scientific and technical literature and present your data within the team 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: • Vocational laboratory technician education (e.g. Apprentas) or master degree in pharmacology, medical physics, bioengineering, biotechnology or related field • Highly experienced in performing animal studies (animal handling, drug application, sampling, animal welfare regulations, small laboratory animal surgery). You have a passion for working with rodents and a drive to perform in vivo oncology pharmacology studies including micro-surgeries, compound administration and preparation of samples for ex vivo analysis. • Good knowledge of standard molecular and cell biology techniques: cell culture, quantitative real-time PCR, transfection, western blotting, cell engineering. Advantageous extra experience is hands-on experience performing small animal imaging modalities such as uCT, ultrasound and bioluminescence imaging. • Strong interest in working in a creative environment where you demonstrate proactiveness, a flexible attitude and scientific curiosity • Well organized with a track record of delivering high-quality results • Excellent English communication skills and motivated to work independently within a global team 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! * 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 353227BR Sep 27, 2022 Switzerland Job Description >9,000! That’s how many associates the Finance Academy has training globally since 2017! The Finance Academy is a platform within Novartis for tailored training offered to Finance colleagues across the world. Our internal faculty is engaged in the development and delivery of a broad program portfolio. Your responsibilities will include, but are not limited to: • Helping plan, organize and run ~15 Finance Academy programs during the year • Supporting on various Finance Academy virtual and live training programs (logistics, preparation, materials, presentations, etc.) • Supporting the Finance Academy coordinator in budget overview and tracking • Helping keep the intranet page up to date Start: November 1, 2022 Duration: 6 months Please apply with your CV and a cover letter explaining your availability for and interest in this position. #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: • Currently enrolled in or recently completed Bachelor’s or Master’s Degree in Human Resources, Finance, Business administration, Communications or Event marketing • Fluent English (written & spoken); good or fluent German is a plus • Strong MS Office skills • Willingness and ability to work in a multicultural environment • Solid organizational skills and the ability to juggle multiple projects at once • Project management experience is a plus Please add a cover letter in which you explain your motivation for the role and mention your availability for starting in November. 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 CORPORATE Business Unit Global Corp. Finance Location Switzerland Site Basel Company / Legal Entity Novartis International 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 354449BR Oct 04, 2022 Switzerland Job Description The Novartis Institutes for BioMedical Research (NIBR) is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Translational Medicine (TM) is the clinical research arm of NIBR and includes about 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. TM Clinical Pharmacology is a cross-functional team, which is specialized on the design, clinical execution and reporting of First-in-Human (FiH) and Clinical Pharmacology studies across all TM therapeutic areas. The operating model is built upon a strategic outsourcing partnership with qualified and specialized CROs, in which the Novartis team maintains sponsor oversight and retains the strategic elements of the studies (e.g. study design, regulatory interactions, project timelines). As part of TM Clinical Pharmacology, you will help to develop therapies for patients, by providing medical and scientific leadership and expertise to support both early and late-stage global programs across all NIBR therapeutic areas in a role that significantly affects the entire Novartis drug development pipeline. Your responsibilities The Medical Director, Clinical Pharmacology (MD CP) will be the primary point of contact for the cross-functional Clinical Pharmacology (CP) Trial Team and for our qualified CROs used in the Clinical Pharmacology Partnership Model for any safety-related, medical and clinical pharmacology-related questions. The MD CP will liaise with the project level Translational Medicine Expert to familiarize with the compound background and program strategy to ensure adequate medical supervision and execution of the study in the best interest of the program and the safety of study participants. The MD CP will also support the project teams with Clinical Pharmacology advice to ensure study designs are optimal to serve the program strategy. 1. Clinical Pharmacology portfolio Efficient and autonomous management and Medical and Clinical Pharmacology leadership for multiple, simultaneously conducted FiH and Clinical Pharmacology studies, including:  Contribution and provision of Clinical Pharmacology expertise for the development of Study Concept Sheets and Protocols  Review of Informed Consent Forms, Statistical Analysis Plans, Tables, Listings and Figure (TLF) shells and drafts, and results summaries  Medical and Clinical Pharmacology coverage for Site Initiation Visits, during the clinical conduct of the trial, for safety reviews and safety reporting and for medical coding  Development of the Clinical Study Report and contribution to publications of study results, including abstracts, posters, manuscripts, plain language trial summaries and technical results summaries. 2. Clinical Pharmacology strategy and initiatives.  Contribution to strategic initiatives and process optimization workstreams in TM Clinical Pharmacology  Strengthening the collaboration with internal stakeholders in early and full development and external partners Impact of this role  This role has a significant impact on the entire Novartis pipeline, by supporting the efficient clinical execution of FiH and Clinical Pharmacology studies for early and full clinical development programs in accordance with the Clinical Development Plan and Clinical Pharmacology Plan, by enabling efficient and result-based decision-making and by delivering key study results to support regulatory submissions.  As a recognized specialist in the field, your strong experience in early clinical development and Clinical Pharmacology will enrich the Medical Team's expertise and will help to build and grow Clinical Pharmacology as the Novartis Center of Excellence for FIH and Clinical Pharmacology studies across all therapeutic areas in the NIBR portfolio.  The Medical Director, Clinical Pharmacology, will further help to strengthen our collaboration with our internal Novartis stakeholders in early and full development and to establish efficient partnerships with our qualified CROs. 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  Medical Degree combined with PhD/post-doctoral and / or specialized further training (board certification) and / or clinical research experience in Clinical Pharmacology.  Previous relevant & significant clinical study experience, across the broad spectrum of Clinical Pharmacology and FIH studies, either in the biopharmaceutical industry leading early phase clinical trials, as a PI or sub-investigator in a CRO or relevant academic medical center, or in a senior role within a CRO responsible for managing the medical relationship with sponsors.  Track record of drug submissions / approval and / or high-quality publications in international scientific journals and advanced training or additional clinical development experience in one of the NIBR TM Therapeutic areas would be an upside.  Full professional proficiency in English (written and spoken). 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 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 347825BR Jul 25, 2022 Switzerland Job Description QC Analyst Microbiology II, Novartis, Basel, Switzerland Unser globales Produktions- und Liefernetzwerk arbeitet 365 Tage im Jahr, um sicherzustellen, dass unsere Patienten die Behandlungen erhalten, die sie für ein längeres und gesünderes Leben benötigen. In dieser Position würden Sie verantwortlich für eine Selbständige, GMP-konforme und termingerechte Durchführung, Auswertung und Dokumentation aller zugewiesenen im Labor anfallenden Arbeiten unter Einhaltung der Analysenvorschriften, SOP's und Sicherheitsrichtlinien. Eigenverantwortung für die Prozesse innerhalb der Laborgruppe und Sorgfalt für die ihm zugeteilte Arbeiten und Gerätschaften sein. Diese Position is gesucht für 2 Jahren. Zu Ihren Aufgaben gehören unter anderem: • Selbständige, Durchführung, Auswertung, Dokumentation und Interpretation von Routineanalysen im Bereich der mikrobiologischen Analytik (z.B. MET, BAN etc.). Löst auftretende Probleme vorwiegend selbstständig • Einhaltung von Terminvorgaben und rechtzeitige Information an Vorgesetzte im Fall von absehbaren Verzögerungen und Problemen • Einhaltung der GMP- und Arbeitssicherheitsvorschriften Pflege, Betrieb und Unterhalt der Geräte und Einrichtungen • Unterstützung des Teams bei Laboruntersuchungen und Problemlösungsfindungen • Selbständige Erstellung von Berichten (z.B. OOS) • Mitarbeit in Projekten 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: • Ausbildung als Biologie-Laborant • Kenntnisse in der MET Analytik sowie über Mikroorganismen und der Umgang mit denselben (aseptisches Arbeiten) sind Voraussetzung • Mindestens 3 Jahre Erfahrung in einem Mikrobiologielabor (zusätzlich zur Lehrzeit), fundierte Erfahrung in Qualitätskontrolle • GMP Erfahrung • Besitzt vertiefte Kenntnisse in allen gängigen Laborrelevanten Techniken (Plattenguss, Filtration, Ausstrich) • Gute Kommunikations- und Teamfähigkeiten • Fliessendes Deutsch in Wort und Schrift / Englisch von Vorteil • IT: Gute Computerkenntnisse, Office-Anwendungen, SAP, LIMS 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 NTO 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 350147BR Aug 09, 2022 Switzerland Job Description 85 quantitative scientists in Novartis are supporting more than 80 clinical development projects in 10 therapeutic areas every day. Come and join an industry leader where you will have the opportunity to provide quantitative sciences support in late-stage drug development. Novartis has an exciting new opportunity for an Executive /Senior Director Pharmacometrics to lead strategy for clinical development programs and manage a portfolio, determine the strategic direction of the development and application of Pharmacometrics methodologies. You will be responsible for leading and optimizing the design and implementation of Pharmacometrics methodologies that help optimize drug development programs across the development organization, lead and optimize the contribution from drug development scientists by consulting with Novartis Institutes for Biomedical Research & Development and Global Medical Affairs partners. You are expected to possess a thorough understanding of clinical development and operational implications and exhibit exemplary leadership skills. Your responsibilities will include: • Ensure PMX strategic contributions to, and influence the direction of, robust clinical development plans and their execution. • Lead in the development of strategic quantitative frameworks for clinical programs in close collaboration with senior management/Development Units as required. • Represent Pharmacometrics science for clinical/submission teams and at regulatory interactions. • Liaise with senior management to influence and negotiate on drug development innovation and clinical development plans with particular emphasis on MIDD strategies. • Take a leadership role in collaboration with partners from other functions to ensure a coherent Pharmacometrics contribution to the development strategy. • As partner to senior clinical and scientific leadership, drive and shape strategic Pharmacometrics input and excellence to drug development across multiple therapeutic or disease areas/indications. • Anticipate Development Unit needs based on in-depth understanding of the relevant Pharmacometrics issues. • Propose or lead functional or cross-functional initiatives requiring coordination of diverse of team members. • Independently represent PMX in due-diligence teams for high-complexity in-licensing opportunities and drive toward steps required to implement a possible deal. • Mentor and develop next generation pharmacometricians. 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: • Ph.D. in pharmacology, biology, engineering, mathematics, statistics, computational science, or a field with significant modeling-related content (or equivalent) • 12+ years of experience in positions with ever increasing relevant responsibilities; 10+ years in applying, innovating, and mentoring model based methods in pre-clinical and clinical drug development. • Expert knowledge and evidence of hands-on experience in the application of Pharmacometrics methods to drug development • Evidence of consulting skill in the drug development context, i.e. within project teams and management boards; experience interacting with regulatory agencies. • Clinical, pharmacological and therapeutic knowledge in one or more disease areas • Proven expert scientific leadership skills demonstrated in facilitating and optimizing the clinical development strategy. • Excellent record of leading the interface to regulatory agencies. • Expert knowledge of drug development and HA guidelines relevant to all areas of Pharmacometrics in clinical drug development. • Excellent communication and presentation skills and in particular the ability to effectively represent Pharmacometrics issues to a wide range of target audiences. • Strong leadership and mentoring skills. Drives and motivates teams and peers. WHY NOVARTIS? 766 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 Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 353285BR Oct 04, 2022 Switzerland Job Description >9,000! That’s how many associates in the Finance Academy has training globally since 2017! The Finance Academy is a platform within Novartis for tailored training offered to Finance colleagues across the world. Our internal faculty is engaged in the development and delivery of a broad program portfolio. In our Corporate (Global Corporate Finance) division we are looking for a responsible, highly professional and agile individual to join our excellent team in the position of a Finance Academy Project Coordinator and Admin! We are welcoming a mature, independent and very people oriented professional like you to lead our administrative project coordination and assistance in delivering the various Finance Academy learning programs, virtually and as face to face. In this role you will leverage technology, look for (and implement) suitable processes to improve both efficiency and customer satisfaction. You will look across Finance Academy programs to identify best practices on effective training/learning delivery and offer support to Head of Novartis Training and Development: Sounds interesting? It is! A unique opportunity for higly motivated and professional people to join us and become an invaluable member of our team. Your responsibilities Finance Academy Coordination (60%): • Leads administrative project coordination in delivering the various Finance Academy learning programs, virtually and F2F. Leverages technology, looks for, and implements, suitable processes to improve both efficiency and customer satisfaction. • Networks and builds relationships with local administrative experts engaged to support the delivery of Finance Academy programs F2F on Novartis campuses world-wide. • Oversees delivery quality and efficiency by Novartis resources in Hyderabad, including training and coaching for continuous improvement. • Maintains accurate dashboards, statistics and training records. • Keeps track of expenses vs. budget, as well as the accuracy of intercompany charges for participant fees. Looks across Finance Academy programs to identify best practices on effective training/learning delivery. • Manages Finance Academy material and assets independently. Administrative Support (40%): • Manages calendar, meetings and ad hoc requests for Head Novartis Finance Training & Development independently and proactively, whilst planning ahead and resolving conflicts. • Organizes travel (flights/visa/hotel/transfer/agenda, etc.) and expenses reimbursement for both operational manager and Director Global Finance Training & Development. • Sets up various meetings in a variety of formats (VC, TC, F2F, external/internal interviews). • Assembles agenda and pre-reads of various team meetings (Finance Academy lead faculty calls, project meetings, etc.) • Supports onboarding of new colleagues in the Finance Academy team by ordering IT equipment, organizing logistics, and setting up onboarding intro meetings. • Maintains various distribution lists and SharePoint sites and manages access rights in a timely way to incorporate people moves. • Manages purchase orders, including GR and invoicing, liaising with Accounting, Sourcing, and vendors on payments. • Organizes mid- and end-year appraisal process for Finance Academy associates and others 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 will bring to the role: • A university degree or “Fachhochschule” in area of Finance, Human Resources, Communication, Business, or similar. • Minimum 3 years of experience as Administrative Expert, with proven capability in managing complex projects and working across borders. • A very people oriented person: Passionate in helping other people grow and develop. • Excellent English (both written and oral). • Knowledge of German is an advantage. • Strong agility and self awareness. • A mature and highly professional individual. *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/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 CORPORATE Business Unit Global Corp. Finance Location Switzerland Site Basel Company / Legal Entity Novartis International AG Functional Area Facilities & Administration Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 352009BR Sep 05, 2022 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. The Compliance, Systems and Operations team in Basel needs you to accelerate one of the most diverse and innovative medical device portfolios in the pharma industry. By creating opportunities for efficient data management for the device design history, you allow us to remove hurdles and enable agile development! You’ll be supporting data driven documentation, automations and improvement projects within the Technical Research & Development Device organization working within a cross-functional teams. In addition, you will have the opportunity to contribute to the development and improvement of key processes for 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: Your responsibilities include, but are not limited to: • Identify sources of data, create data model and database structure for medical device related information and data. • Create or define search model for a device database • Working with stakeholders to identify inefficiencies and obstacles to leaner processes. • Help to create and/or improve procedures and processes to facilitate development of devices for 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 What you’ll bring to the role: • Master Student in Engineering, Biotechnology or Life Science, Computer Science or Computer Engineering. Quick learner, quality focused, good communication and collaboration skills, autonomous and self-driven. • Knowledge in data structures and databases (e.g. SQL) as well as process automations (like Power Apps or Power Automate). • Programming skills in Python, Xml, html, Java or similar programming languages. • 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 consider Novartis? 750 million. That’s how many lives our products touch. 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 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 354305BR Oct 05, 2022 Switzerland Job Description The musculoskeletal disease area at NIBR in Basel is seeking a motivated intern to develop their scientific curiosity by studying novel mechanisms of cartilage regeneration and repair to help develop transformative therapies for osteoarthritis. Our labs are dedicated to studying cartilage homeostasis and repair using mesenchymal stem cells, mature chondrocytes, and other cell models. The successful candidate will perform in vitro experiments in these cell models to support projects related to cartilage repair and osteoarthritis. The project will primarily include molecular and cellular biology techniques, such as RNA purification, qPCR, siRNA/CRISPR, cell culture, protein overexpression and protein quantification (Western blotting). Timing: Start in January – April 2023 Duration: 6 months Your Responsibilities: • Molecular biology (RNA purification, qPCR, siRNA KD, CRISPR KO) • Cellular Biology • Protein overexpression and quantification (Western Blot) • Planning, execution, documentation, analysis, and interpretation of experiments 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 Degree (graduation no longer than one year ago) or currently enrolled in a MS program in biology, biotechnologies or biochemistry • Fluency in English, both written and spoken, is a requirement • Good general IT knowledge, especially in MS Office applications • Good knowledge in molecular and cell biology, biochemistry, and cell culture • Previous experience in cell culture • Excellent communication and organisational skills 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!Division NIBR Business Unit MUSCULOSKELETAL - 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 352971BR Oct 05, 2022 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. As a software developer embedded in the NIBR Biologics Center (NBC), you will bring an expertise in front-end and back-end development. You will be responsible to develop software solutions to support the development and in particular the immunogenicity assessment of breakthrough Biologics. As a team member of our Bioinformatics team, you will be in direct contact with our scientific partners to gather requirements and specify the corresponding technical solutions. You will work independently in a dynamic team under the supervision of a Senior Expert. Responsibilities will include but are not limited to: • Conduct interviews with scientific partners • Create technical specifications • Develop front-end and back-end solutions 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/MSc or equivalent education in software development, bioinformatics, or a related discipline. • Proficiency in front-end and back-end development. In particular in the following technologies: Java EE, Tomcat, REST Web services, Web development, HTML / CSS, JavaScript, Linux Shell Scripting • Ideally with HPC experience, Git / BitBucket • Other beneficial skills include: Oracle SQL, JSP, Python, R • Basic knowledge about business and requirement analysis is required. • Diligent and accurate working style, as well as communication and organizational skills are required. • Ability to be a self-motivated and independent team player able to thrive in a dynamic matrixed working environment. • Practical experience in an industry setting and basic knowledge about Biologics and immunogenicity would be of advantage. • Proficiency in English (oral and written), German and/or French of advantage. Contract Start: Nov 1st, 2022 – Apr 30th, 2023. Duration: 9 months *Some restrictions on flexible working options may apply and will be discussed during interview if applicable. 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 BIOLOGICS NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Data Science Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 347289BR Oct 03, 2022 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 a Research Scientist to carry out cutting-edge oncology drug discovery pharmacology research. We seek an experienced, motivated and ambitious individual with a passion for in vivo oncology research. You will join the Radioligand Therapy team to develop and validate novel targets in our world leading Oncology portfolio. The position is based at the Novartis Institutes of BioMedical Research (www.nibr.com) in Basel, Switzerland. The ideal candidate should have a passion for working with rodents and a drive to perform in vivo oncology pharmacology studies including micro-surgeries, compound administration and preparation of samples for ex vivo analysis. Hands-on background performing small animal imaging modalities such as PET/SPECT/uCT or in cell biology techniques is a plus. The successful candidate will work collaboratively as an integral part of global projects and be an active member of lab and project teams. Responsibilities include but are not limited to: • Develop and characterize novel in vivo oncology models • Perform efficacy studies with cutting edge radioligand therapies • Perform biodistribution studies and metabolites analysis • Perform pre-clinical imaging studies including PET/SPECT/uCT • Design, perform and evaluate various in vitro and ex vivo assays (e.g. cell culture, transfections, IHC, proliferation assays, immunofluorescence, PCR, Western blotting, FACS) 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: • Masters degree in pharmacology, cell biology, medical physics, bioengineering, biotechnology or related field or Bachelors degree with equivalent experience • Practical work experience in biomedical research from an industry or academic laboratory • Experience in performing animal studies (animal handling, drug application, sampling, animal welfare regulations, small laboratory animal surgery) • Self-motivated, proactive, and able to work independently Desirable requirements • Knowledge and experience of standard cell biology techniques is desirable: cell culture, IHC, FACS, quantitative real-time PCR, transfection, western blotting, cell engineering etc • Highly collaborative team player that enjoys working across multi-disciplinary teams • Excellent organizational and communication skills • Knowledge of cancer biology 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! * 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 348934BR Sep 19, 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. 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. As the leader of Global Clinical Team(s) (GCT), the GPCH is accountable for the design, implementation, and execution of a clinical development program(s) to support decision milestones, regulatory requirements, market access and owns the risk benefit-assessment for the program(s). The GCPH contributes to the disease area strategy. Your responsibilities include, but are not limited to: • Leading the GCT and representing Clinical Development on the Global Program Team (GPT) • Leading 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, pharmaco-economic dossiers) with high quality and consistency with Integrated Development Plan (IDP) and Target Product Profile (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) • 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) • Post-DDP, leading the development and execution of the clinical strategy. Developing an endorsed (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 • Where applicable, supporting Business Development & Licensing (BD&L) activities 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 (preferred), PhD, or PharmD degree required, specialization in Hematology or Oncology. Advanced training/knowledge in CAR-T and clinical experience preferred • 10 years (PhD or PharmD) of involvement in clinical research or drug development in an industry environment spanning clinical activities in Phases I through III/IV, including submission dossiers • Advanced knowledge of assigned therapeutic area preferred, 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 and results • 5 years people management experience required; this may include management in a matrix environment • Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, and regulatory/clinical development process • Experience with submissions and health authorities required. *Some restrictions to flexible working models may apply and will be discussed at interview if applicableDivision 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 354316BR Oct 03, 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 351656BR Sep 21, 2022 Switzerland 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. Chemical Biology & Therapeutics (CBT) is one of the platforms in NIBR, where teams with diverse backgrounds and diverse scientific expertise catalyze collaboration and apply their unique skills to translate exceptional science into medical innovation. Our associates are grouped by their professional expertise and capabilities in so-called Homes. This position will be in Genomic Sciences Home, in which you will be working in an open, interdisciplinary and collaborative environment with molecular & screening biologists, data scientists, medicinal chemists and automation engineers to design, develop and perform complex high throughput experiments and establish next generation assays. You are a curious, creative, scientifically agile and self-motivated scientist with strong communication skills who is interested in making an impact on drug discovery through scientific technologies with the focus of improving patient’s lives. In doing so, you will have opportunities to develop and grow your professional network across NIBR and beyond. We are looking for a highly motivated, collaborative, research associate with automation, liquid handling, and cell-based assay development experience to support our functional genetics team in Basel, Switzerland. Main responsibilities include but are not limited to: • Responsible for leading target identification studies by deploying plate-based genetic and genomic methodologies • High affinity to liquid handling, automation and programming of automated assay schemes • Collaborate with project teams and platforms to jointly identify best strategy and implement automated cell-based assays • Conduct plate-based genome-wide genetic experiments in complex disease models • Analyze and interpret generated data. Propose next steps to team, effectively document and communicate results to a variety of audiences • Agility to navigate and be successful in an interdisciplinary, fast-paced, matrixed work environment 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 or equivalent (non-PhD level) in a relevant life Science disciplines (Biology, Chemical Biology, Bioengineering, or related fields) • At least 2 years of relevant work experience • Proven track record of setting up cell-based screens • Proven track record of setting up screening automation solutions and implementing liquid handling schemes • Hands-on expertise of lipofection, electroporation and viral delivery systems • Basic data handling and statistical analysis skills • Fluency in English is essential (oral/written); advanced knowledge of German and/or French is a plus Additional advantageous skills: • Experience of working with different plate readers, knowledge of Biomek and Sami software • In-depth knowledge and hands-on expertise with biological or chemical probes and experience in gene-editing • Advanced knowledge of German and/or French 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 CBT - 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 351814BR Sep 17, 2022 Switzerland Job Description 5600! That’s the number of the associates in the Novartis Institutes for BioMedical Research (NIBR). NIBR is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. As our Principal Scientist in the Oncology Drug Discovery Biology unit, your role will be Junior Lab Head employing ground-breaking technologies to mechanistically dissect the function of novel targets with putative oncogenic properties and provide detailed characterization of the mechanism of action of novel molecules. To be successful in this role you will be a team player with a versatile profile, knowledge in molecular biology, functional genomics, genome/proteome-wide technologies, protein science and familiarity with computational tools to advance technological expertise within the department. Major accountabilities include: • Plan and implement wet lab experiments to address key scientific questions outlined for various project • Apply a statistically rigorous framework to interrogate large scale datasets to drive project progression and formulate novel scientific hypotheses • Implement cutting-edge technologies critical for target identification, validation and structure/function studies • Act as a reference person for technology implementation and contribute to various projects around target identification, fundamental biology, drug discovery and translational research within multidisciplinary teams • Closely work with multiple teams across expertise groups within Oncology and across departments in the global organization • Guide, supervise and develop scientific associates • Present concepts and projects in a clear, scientifically sound, and data-driven, objective manner in different settings and venues • Manage lab resources in a flexible manner to adapt to changing priorities 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 • Ph.D. in Cancer Cell Biology, Molecular Biology, Biochemistry or related field with limited postdoc experience (maximum 5 years). • State-of-the-art experimental expertise in molecular and cellular biology to perform mechanistic studies and structure-function analyses • Proficiency in using R and/or Python to wrangle and visualize large scale datasets is required. • Highly collaborative and self-motivated team player with pro-active interactive attitude across a large and diverse environment • Approachable attitude and motivation to mentor junior lab members • Strong track record of scientific accomplishment at high standards • Excellent communication and presentation skills in English These skills are a strong advantage: • Familiarity with functional genomics, genome-/proteome-wide technologies or protein science techniques. • Familiarity with Linux/UNIX. Closing date for applications: October 10th, 2022 Division 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 354233BR Sep 30, 2022 Switzerland Job Description 100 000! That's how many unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world - Novartis Group is looking for a Legal Trainee with a Swiss law degree (MLaw), who is passionate about gaining first-class, hands-on in-house legal experience within a multinational environment of a leading pharmaceutical company. We are offering a 6-month legal trainee position starting on: - April 1, 2023 and ending on September 30, 2023. and - September 1st, 2023 ending on February 29, 2024 Your responsibilities include, but are not limited to: • Support the Group Legal team by providing legal advice mainly in the area of employment law, including contentious and non-contentious HR matters and global and local projects • Assist with the drafting and reviewing of a variety of agreements, internal guidelines and templates • Draft legal memoranda on a wide variety of legal issues and disputes #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: • Swiss Law degree (Master of Law, has to be on Swiss Law), master's degree needs to be completed before start date • Fluent written and spoken English and German is a must • High motivation and ability to work independently • Prior legal internship is a plus Please submit your complete application (CV, cover letter and your academic records) online and state your availability (from April 1 or September 1) in your cover letter. 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 CORPORATE Business Unit GROUP LEGAL Location Switzerland Site Basel Company / Legal Entity Novartis International 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 351615BR Sep 16, 2022 Switzerland Job Description 250+ active clinical trials are supported by Global Clinical Supply (GCS), 50’000 shipments are shipped annually and 1 million patient kits are packaged. Our vision is to become a smart and agile company that delivers more products to more patients more efficiently. The Postgraduate Program allows you to experience the daily business in a global leading pharmaceutical company. Joining the GCS 2 years rotation program as an intern offers you an outstanding opportunity to gain insight into the activities of two different functional areas - Clinical Packaging Operations and Supply Chain Management. The Process Expert in the Clinical Packaging Operations team has operational end to end responsibility for manufacturing of primary packed and clinical finished goods in compliance with the regulatory guidelines, SOP’s and internal regulations. You will support the daily work, including handling of innovative projects and improving existing processes. The Supply Chain Manager in the Supply Chain Management team secures demand and supply planning in GCS, carrying out this responsibility from Drug Substance (DS) to Clinical Finished Goods (CFG). The team works towards alignment not only within GCS but as well across other functions at Novartis and Clinical Manufacturing Organizations. 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 Your responsibilities include, but are not limited to: Operations team: • Support the Process Experts in daily tasks (e.g. monitoring, logbook checks) • Support Clinical Packaging in the definition and implementation of suggestions for improvement of production performance and reduce the risk of deviations • Support cleaning validation activities • Be a "Certified Deviation Investigation Owner" (if applicable) • Be an expert on GMP for Clinical Packaging areas (e.g. primary / secondary packaging, label printing, dispensation) Supply chain Management team: • Support the Supply Chain Manager to create an End to End supply plan from clinical Finished goods (CFG) to Drug substance • Supports the optimization of safety stocks and inventory levels at Primary packed and CFG level together with the other line functions • Supports the Supply and Operational Process on Demand and Supply of clinical and technical goods • Actively participate in team activities and supports the fulfillment of all related tasks and responsibilities related to operational discipline • Proactively communicates key issues and any critical topic in a timely manner to the appropriate management level, senior colleague or Team Head • Ensures compliance of processes with regulations as well as Novartis internal procedures and GxP requirements such as Change control process Minimum requirements What you’ll bring to the role: • Recent Master graduate (graduation not longer than 1 year ago) in Pharmacy or related field • Fluent in German and English (written and spoken) is a must • Enthusiasm for pharmaceutical production, packaging and supply chain • Good communication, negotiation and presentation skills • Good organizational and planning skills • Problem-solving oriented and working skillfully in interdisciplinary teams • Soft skills: self-driven, motivated, willing to learn, strong team spirit Start date: January 2023 or upon agreement Duration: 24 months Why consider Novartis? 799 million. That’s how many lives our products touch. 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 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 347287BR Jul 08, 2022 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 biodistribution studies and metabolites analysis for novel RLT drug candidates in rodent oncology models • Perform pre-clinical imaging studies including PET/SPECT/uCT • Complete in vitro characterization (e.g. plasma stability, protein binding, cellular uptake) • 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 (Target Identification and Validation, Drug Discovery Biology, Cellular Assays, Enzymology and Biochemistry, Pharmacology) • 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 Desired qualification • Experience with PET/SPECT/uCT imaging with mice and rats • Basic understanding of experimental design, data analysis and interpretation of imaging data • Experience in cellular and molecular biological methods (in particular cell culture, cell viability assays, transient/stable cell line generation, immunoblotting, ELISA) • Experience with immunohistochemical analysis, tissue processing and sectioning • Used to successfully work within a high productivity and quality environment • Proven ability to effectively collaborate in an interdisciplinary team environment and across sites • Highly collaborative and self-motivated team player • Excellent organizational and communication 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! * 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 352733BR Sep 28, 2022 Switzerland Job Description 28,000 associates of more than 100 nationalities deliver high quality and affordable medicine on time, every time, safely and efficiently. We are offering a 6-month legal trainee position to support the Novartis Operations Legal department on a wide range of legal matters and projects in areas such as contract law, commercial law, M&A and licensing transactions, restructuring, antitrust law, pharmaceutical/healthcare laws and regulations, intellectual property and disputes/litigation. This legal trainee position offers excellent opportunities to gain first-class, hands-on in-house legal experience within the stimulating, multinational environment of a leading pharmaceutical company. Duration: 6 months Start: March 2023 Your responsibilities will include: • Support M&A projects, business development & licensing transactions (product divestments, acquisitions, in-licensing and out-licensing), portfolio and manufacturing site divestments, including conducting due diligence, managing data rooms and Q&A processes, and legal implementation of deals • Support a diverse range of commercial matters relating to the development, procurement, manufacturing, quality assurance and supply chain and distribution of pharmaceutical products • Support diverse range of legal department projects, e.g. contract templates, legal trainings, global legal research projects, digitalization, outsourcing, etc. • Assist with the drafting, negotiation and review of a variety of transactional, commercial and technical agreements • Draft legal memoranda on a wide variety of legal issues and disputes • Provide legal advice to internal clients • Draft document and key position summaries • Interact with Novartis global, regional and country legal network • You will be supervised and guided by a range of lawyers on different levels of the company, ensuring a great learning experience #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: • Swiss Law degree (Master of Law or equivalent, has to be on Swiss Law), master's degree needs to be completed before start date • Business-level English skills (written and spoken), additional language is a plus • High motivation and ability to work independently Desirable: • Prior legal professional experience in a law firm, court or legal in-house department (internships etc.) would be helpful. We are also open to applicants without prior experience who have a strong interest and are motivated to learn on the job • Other professional experience in the corporate environment is a plus Please apply with your CV and a cover letter mentioning your 6-month availability starting in March 2023. 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 LEGAL 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 352745BR Sep 14, 2022 Switzerland Job Description Thousands of assays are currently available for searching, browsing and analysing, as part of NIBR's large and growing collection of in-house 'omic data. Become a part of the data revolution in drug discovery and work with experienced data scientists and engineers to learn how to leverage these data to reimagine medicine and improve lives! We are seeking a highly motivated intern to work on data integration, visualisation, analysis and/or computational modelling as part of the Oncology Data Science team at NIBR Oncology, supporting our cutting-edge oncology drug discovery programs. Timing: Q4 2022 (expected start date) Duration: 6 months Your responsibilities: • Impact drug discovery projects by developing pragmatic analytical or computational modelling solutions • Writing code to process and analyse ‘omics data (high throughput screening, RNASeq, scRNASeq) in a high-performance computing environment • Working as part of a multidisciplinary team to integrate in-house data with publicly available datasets • Contributing to a range of data science projects depending on student interest and skillset, from visualisation and data ingestion to in-depth analysis to building machine learning models to answer key scientific questions 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 or Master degree or higher in Computational Science / Bioinformatics or a related discipline. • Very good English spoken & written • Experience using the R programming language (Bioconductor / Tidyverse / RShiny). • Experience applying workflows and software to analyze complex data sets • Some knowledge of biological sciences, genetics & genomics • Clear communication to explain how and why an analytical method was used Desirable: Experience using deep learning frameworks (PyTorch or similar) for computational modelling 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 NIBR Business Unit Oncology 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 351036BR Sep 12, 2022 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. As Senior Data Visualisation Engineer, you will be a member of our team which helps to understand complex and critical business problems then formulate integrated analytical approaches (mine data sources, employ statistical methods and machine learning algorithms) to contribute to solving unmet medical needs and discover actionable insights. Your key responsibilities will include but are not limited to: • Innovate by transforming the way to solve a problem using Data Science and Artificial Intelligence. Articulates solutions /recommendations to business users. Presents analytical content concisely and effectively to non-technical audiences and influences non-analytical business leaders to drive major strategic decisions basis analytical inputs • Coordinates, prioritises and efficiently allocates the team resources to critical initiatives: plans resources proactively, anticipates and actively manages change, sets stakeholder expectations as required, identifies operational risks and enable the team to drives issues to resolution, balances multiple priorities and minimizes surprise escalations • Collaborates with internal stakeholders, external partners and Institutions and cross-functional teams to solve critical business problems, propose operational efficiencies and innovative approaches. • Proactively evaluates the need of technology and novel scientific software, visualisation tools and new approaches to computation to increase efficiency and quality of the Novartis Data Sciences practices • Provides agile consulting, guidance and non-standard exploratory analysis for unplanned urgent problem • Independently identifies research articles and reproduce / apply methodology to Novartis business problems • Publishes in peer reviewed journals, helps organizing sessions at external professional conferences and contributes to cross-industry work streams in external relevant working group • Makes right choices from a breadth of tools, data sources and analytical techniques to answer a wide range of critical business questions • Ensures exemplary communication with all stakeholders including senior business leaders • Contribute to the development of Novartis data science capabilities. 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: • 10+ years of relevant experience in Data Science • 5+ years of relevant experience in Data Science, Information & Decision Theories, Data Visualisation, Machine Learning & Deep Learning, Big Data, Applied Mathematics, Predictive Modelling & Data Management 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 NIBR Business Unit Oncology NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Data Science Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 351027BR Sep 06, 2022 Switzerland Job Description As Senior Principal User Researcher (UX), you will be a member of the Business Engagement team in the Novartis Institutes for BioMedical Research (NIBR) Informatics team in Switzerland. Our team helps to analyse and triage incoming demand from our scientific stakeholders, so that our product organization can focus on delivering products and services that create maximum value, impact, and outcome. This is a global team with around 20 associates, composed of Business Relationship Managers, Business Analysts, User Researchers, Designers & Data Visualisation experts in Basel and Boston/Cambridge in the US. We support the entire product development lifecycle, from early problem discovery to product delivery, and retirement of products from a non-technical point of view. Your key responsibilities will include but are not limited to: • Execute early problem discovery on incoming business demand, identify the underlying stakeholder needs and problems, and map them back to organisational goals and strategies defining the desired impact & outcome. • Collaborate with our scientific stakeholders on various levels in the organisation, business relationship managers, and product teams to understand user and stakeholder research needs and select the right methods to accomplish research goals. • Serve as a User Researcher on one or more product teams at various stages in the product lifecycles, from early problem discovery to product delivery. • Lead user and stakeholder research activities from strategic problem discovery, foundational user and stakeholder research, and product testing. • Provide high quality research deliverables to the product team and other stakeholders • Evangelise user centered design and specifically how, when, and why user research should be part of our product development process. • Coach and train team members in user research methodologies on the job. 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) in HCI, Human Factors, Psychology, or a field related to User Experience, with experience in scientific (Pharma) UX and User Research, business analysis, and/or stakeholder management. • 3-5 years of experience working in cross-functional teams as a User Researcher in Pharmaceutical or Biotechnology companies ideally in a biomedical research setting. • Effective interpersonal, communication, negotiation, and collaboration skills. • Ability to communicate and understand complex scientific concepts in both technical and non-technical terms. • Excellent presentation and meeting and workshop facilitation skills. • Strong customer orientation and the ability to map customer needs to enterprise level systems and data. • Innovative and motivated with an ability to foster a positive working environment. • Capable of collaborating with a community of research scientists to define solutions, which solve an underlying problem. • Strong ability to handle multiple assignments at one time while working independently and effectively under deadlines. 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 NIBR Business Unit CBT - NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Information Technology Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 351399BR Sep 09, 2022 Switzerland Job Description 6000! The number of associates working across the globe for Novartis Institute of Biomedical Research (NIBR). By joining NIBR, you be working in a global and exciting research and development environment, fueling the pipeline through proof of concept and reimagining medicine. Based on our understanding of cancer, Translational Clinical Oncology (TCO) will design and execute innovative exploratory clinical trials in order to develop the next generation of highly effective therapeutics that transform the lives of patients with cancer. As part of the Data Analytics and Review team (DART), you will apply groundbreaking technologies and analytic approaches to support the TCO portfolio. If you are curious to support the clinical team in exploratory analysis of patient data, this could be the opportunity for you! Your responsibilities will include, but are not limited to: • Act as a key functional expert who manages, advises and coordinates the activities of a specific assigned area, project or team of experienced specialists • Build TCO clinical operational digital tools and provide data visualization strategies • Lead the decision‐making process for establishing multidisciplinary project/program goals within own team whilst defining team goals, aligning and providing input to department strategy • Effective use of resources through operational excellence and driving continuous improvement in clinical data review and data visualization • May act as a subject matter expert for key operational areas influencing respective function • Understand Health Authority requirements and participate in Health Authority inspections as required • Lead and support clinical and non-clinical special projects and initiatives, oversight of DART deliverables based on business needs 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: • BA/BS/MS or international equivalent experience in data science, statistics, computer science, mathematics or life sciences or related field • For Manager Level: approximately 7 years of experience in drug development and 5 years in clinical data operations • For Associate Director Level: approximately 10 years of experience in drug development and 8 years in clinical data operations • Project management experience: expert experience in contributing to data review plan and statistical analysis plans and/or constructing technical programming specifications with experience leading several projects, portfolio-level activities, preferably in Oncology, including coordination of a large team of internal or external programmers • Expert R/Rshiny or Python or SAS experience and proven skills in the use of SAS or R/Rshiny within a programming environment to develop and validate deliverables, proven experience in development of MACROs • Knowledge of CDISC data structures as well as a solid understanding of the development and use of standard programs. Experience in JReview, digital Patient Profile, Spotfire, Tableau or other data visualization tools is a big plus • Understanding of regulatory requirements relevant to Statistical Programming (e.g. GCP, ICH) and clinical study practices, procedures and methodologies 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 TCO NIBR 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 351041BR Sep 01, 2022 Switzerland Job Description Novartis Pharma is hiring a Postdoc in Chemical & Analytical Development (CHAD), enrolled in the dynamic Early Talent Program (ETP). The department plays a crucial role in the development of processes for manufacturing and analysis of Small Molecule Drug Substance from the time it leaves the discovery laboratory until it is handed over to Commercial Production. Candidates will work in close collaboration with a senior chemist and laboratory technician(s) and be involved in the design and development of safe, ecologically benign, and economic manufacturing processes for chemical intermediates and drug substances. This program strives to: -Provide good working experience to students -Evaluate new methodologies at the state of the art of the chemistry -Gain expertise in new technologies of interest. The Early Talent Program is designed to offer highly motivated talents outstanding insights into drug development. This year we provide the opportunity to work in the emerging field of data sciences linked to chemistry. Several rotations of 3 - 12 months within various groups in CHAD Basel (e.g. continuous manufacturing, chemical development unit, bio catalysis team) including close interaction with our colleagues in Changshu, China, will provide a comprehensive overview of drug development within Novartis. During these rotations, you will be exposed to current standards in safety, quality and training systems and good manufacturing practice (GMP). You will not only be able to transfer your theoretical know-how into practice, but also to develop your soft skills and grow your internal network for your future career in the pharmaceutical industry. We are looking for a highly motivated recent PhD to support and expand the development of data science expertise across our chemical development organization. Your responsibilities will vary throughout the program stages and include: - Evaluate and build groundbreaking (raw) data collection, visualization, and analysis to support innovation as well as chemical process and product quality improvements - Apply data analysis tools to improve chemical process understanding, in the small molecule and mixed modalities area, using, e.g. multivariate data analysis, statistics, machine learning, data-driven models, etc. - Support development of laboratory automation (e.g. ChemSpeed, HiTec Zang) and PAT systems as well as PAT applications for process control/understanding of chemical and pharmaceutical manufacturing - Deploy models to support the scientific project team with relevant IT platforms (e.g. Spotfire, KNIME, R, Python, etc.) - Develop methods for model-based experimental design and chemical process optimization, e.g. Bayesian statistics - Participate and actively contribute to scientific exchange groups within Novartis, including data science, computational chemistry, lab automation as well as molecular modelling (e.g. screening for biocatalytic processes). 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 Preferentially, a completed PhD in chemistry, chemical engineering, pharmaceutical sciences, life sciences, process engineering, data science, applied statistics or related subject area - Strong chemical, pharmaceutical or engineering knowledge required - Extensive experience in data science, good knowledge of relevant software and sophisticated digital skills are required - An excellent record of data science application in innovative chemical and/or pharmaceutical areas - Insights or experience in pharmaceutical or life science industry is an advantage Soft Skills: - Ready to work in international and multidisciplinary teams - Open minded and curious personality paired with “can do” demeanor - Strong interpersonal and communication skills are required - Proficiency in English. German or French skills are advantageous Duration of employment: 24 months Why consider Novartis? 766 million. That’s how many lives our products touched in 2021. 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!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 352028BR Sep 29, 2022 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 to join a laboratory that carries out cutting-edge oncology drug discovery pharmacology research. We seek an experienced, motivated and ambitious Research Scientist * wishing to continue a successful scientific career in a fast-paced drug discovery environment. You will work collaboratively as an active member of lab and global project teams using a wide range of in vivo and in vitro techniques, closely interacting with your lab head and colleagues. You will join the Global Oncology Drug Discovery group contributing to develop novel cancer therapeutics and bring innovative targets into our world leading Oncology portfolio. The position is based at the Novartis Institutes of BioMedical Research (www.nibr.com) in Basel, Switzerland. Responsibilities include but are not limited to: • Design, perform and evaluate experiments to characterize novel drug candidates for oncology projects in various in vitro and ex vivo assays (e.g. cell culture, transfections, proliferation assays, ELISA, PCR, Western blotting, FACS) • Develop and characterize novel innovative in vivo oncology models using molecular imaging techniques • Independently search for information in scientific and technical literature and present your data within the team 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: • Vocational laboratory technician education (e.g. Apprentas) or master degree in pharmacology, medical physics, bioengineering, biotechnology or related field • Highly experienced in performing animal studies (animal handling, drug application, sampling, animal welfare regulations, small laboratory animal surgery). You have a passion for working with rodents and a drive to perform in vivo oncology pharmacology studies including micro-surgeries, compound administration and preparation of samples for ex vivo analysis. • Good knowledge of standard molecular and cell biology techniques: cell culture, quantitative real-time PCR, transfection, western blotting, cell engineering. Advantageous extra experience is hands-on experience performing small animal imaging modalities such as uCT, ultrasound and bioluminescence imaging. • Strong interest in working in a creative environment where you demonstrate proactiveness, a flexible attitude and scientific curiosity • Well organized with a track record of delivering high-quality results • Excellent English communication skills and motivated to work independently within a global team 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 351597BR Sep 12, 2022 Switzerland Job Description Oncology Translational Research at Novartis Institutes for Biomedical Research is recruiting an independent scientist with a strong background in cellular and molecular biology to join the Oncology Pathology and Biomarkers group in Basel, Switzerland. We are seeking a highly motivated scientist with at least 3 years of experience in pre-clinical/translational research within the pharmaceutical industry or in an academic laboratory. You will be responsible for the generation of novel, high quality data to progress research programs to the clinical trial stage. By using a variety of molecular and cell biology approaches you will design, perform, and analyze studies using human tissues, xenograft models and cell lines, applying techniques like immunofluorescence microscopy, qPCR, western blotting, and other cutting-edge technologies. Your work will contribute to the identification of molecular predictors of response to cancer drugs and resistance, and to the discovery of potential combination therapies. While closely interacting with your lab head and colleagues in the group, you will be expected to flexibly contribute to local and global projects as needed and to proactively share knowhow and experience across groups. Major accountabilities include: • Independently design and perform experiments with a high degree of complexity, demonstrating expertise in a wide range of techniques (e.g., IF, cell culture, immunoblotting, qPCR). • Understand role of biomarkers in FIH studies and assay validation process, support development of biomarker assays to implement in the clinic internally and externally. • Be a self-starter and independently seek out opportunities to learn and contribute within Oncology and the larger NIBR organization. • Work collaboratively with others in the group and project team members. Communicate directly with project teams to design and execute experiments, and subsequently present and discuss results. • Recognize problems and troubleshoot. • Represent the lab at project team meetings. • Contribute to report writing and other publications. • Actively participate in supporting, teaching, and learning from colleagues in the Oncology Pathology and Biomarkers group. • Fully understand and participate in the drug development process, including reaching out to and working with early discovery and late development teams for project specific questions. • Contribute to the efficient management of a functional laboratory, including maintenance of technical equipment and compliance with human tissue guidelines. 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 BSc or qualified Lab Technician (apprenticeship/vocational training) in Cellular Biology, Molecular Biology, or other relevant discipline • Advanced/Fluent English oral and written • 3 years of practical work experience in biomedical research in industry or academic laboratory • Proficiency and hands-on experience in applying a wide range of cellular and molecular biological methods, such as qRT-PCR, cloning, CRISPR, cell culture, cell viability assays, transient/stable cell line generation, immunoblotting, and ELISA • Basic experience using basic bioinformatics tools to support experimental design, data analysis and interpretation is considered a plus • Knowledge of cancer signaling/biology is additionally preferred • Experience working successfully within a high productivity and quality environment • Proven ability to effectively collaborate in an interdisciplinary team environment • Highly collaborative and self-motivated team player • Excellent organizational and communication skills Why Novartis? 767 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 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 348974BR Aug 04, 2022 Switzerland 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. Chemical Biology & Therapeutics (CBT) is one of the platforms in NIBR, where teams with diverse backgrounds and diverse scientific expertise catalyze collaboration and apply their unique skills to translate exceptional science into medical innovation. Our associates are grouped by their professional expertise and capabilities in so-called Homes. This position will be in Protein Sciences Home, which focuses on producing proteins for 3D structure and biophysics to characterize their interactions with other molecules to discover new ligands, validates hits, identifies targets from hit and determines how these ligands interact with their targets. We are seeking a passionate, curious, and collaborative protein scientist with demonstrated experience in expression optimization and characterization of challenging proteins. You will carry out the exciting task of studying disease-relevant protein targets. Expertise of protein expression in suitable hosts, extensive optimization and development of effective small-scale workflow is key to successfully scale up protein production that is needed for drug discovery activities. You are an empathic listener and a key team player who thrive in a multicultural matrix environment. In doing so, you will have opportunities to develop and grow your professional network across NIBR and beyond. Your responsibilities Your responsibilities include, but not limited to: • Understand complexity of protein expression in eukaryotic hosts, executes experiments and interpret data to define logical and innovative path forward. • Key contributor in providing quality protein to support diverse project activities. You are motivated by troubleshooting activities to bring a success within competitive timeline. Identifies scientific/technical trends within own discipline that impact projects. • Empowered to carry out novel research and/or technical activities remaining within the interest of department focused on expression of challenging protein targets. • Actively mentor, train, and support team members, especially in own area of deep expertise. Contribute to develop objectives for team, together with broader team members. • Influence a constructive culture within functional community, friendly with collaborative mindset and willing to grow as an inclusive leader. 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 • Thorough understanding of theoretical and technical principals of protein expression in eukaryotic hosts. • Expert knowledge of handling commonly used expression hosts with extensive experience in producing diverse protein families using eukaryotic hosts (HEK, Insect cells, etc). • Proven record of accomplishment(s) in troubleshooting expression optimization and scale up. • 5-10 years experience in expression, optimization, and scale-up of protein production. • Master’s degree in biochemistry, microbiology, biotechnology or bioprocess technology with minimum of 5 years of experience in medium/high-throughput protein production set up. Or Bachelor’s degree in above mentioned field with minimum of 10 years of experience. • Experience of leading a team in above mentioned area. • Fluent in written and spoken English with effective presentation skills. • Skilled user of Microsoft applications (Word, Excel, Powerpoint) and data management (data capturing, processing, analysis and reporting). Desirable requirements: • Background of bioprocess technology and unit operation is a plus. • Experience in cell line development. • Experience in expression, purification, and characterization of membrane proteins. • Strong desire in technology innovation and happy to work in a background to build successful team. • Previous experience of working in protein production facilities is a plus. 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 NIBR Business Unit CBT - 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 352549BR Sep 28, 2022 Switzerland 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 Biotherapeutic Engineering and Gene Therapy (BEGT) group is a part of the NIBR Biologics Center (NBC). BEGT drives a diverse portfolio of modalities including therapeutic proteins, multi-specific antibodies, CAR-T, RNA therapeutics, AAV and lentiviral vectors. As a Principal Scientist, you will further strengthen our protein engineering team in Basel by bringing expertise in protein-based therapeutics. You will join a dynamic team working closely with Disease Areas to establish new strategies made possible by the design of next generation biotherapeutics. Your responsibilities include, but are not limited to: • Protein engineering in general with focus on bi-/multispecific formats. • Enhance our protein engineering platform and develop novel technologies to expand our discovery of bi-/multispecific biotherapeutics. • Collaborate with Disease Areas to solve therapeutic challenges by design of the next generation of recombinant biotherapeutics. • Collaborate within other units inside NBC to profile functional and biophysical properties of designed molecules. • Present experimental designs, protocols, results and interpretations to a varied audience • Maintain familiarity with current scientific literature and techniques in the field of bi/multi-specific formats. • Demonstrate good organizational and communication skills. Expected to be accountable for effectiveness and timelines of completion of project goals. • Ability to balance multiple projects under a demanding timeline. 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 • Ph.D. Cell Biology, Molecular Biology, Biochemistry or related field with 2+ year of relevant experience or M.S. with 6+ years relevant experience. • Significant experience in protein engineering methodologies and applications for immunotherapies. • Experience mentoring bench scientists either directly or as a matrix team lead. • Strong organizational, time management, communication, and interpersonal skills. • Comfort in a fast-paced environment and ability to adjust workload based on changing priorities, coupled with a demonstrated eagerness to learn new things. • A strong self-starter, independent thinker with strong attention to detail. Desirable: Hands on experience in expression, purification and characterization of recombinant proteins. Hands-on experience in HTP-based binding assays and/or cell-based assay. Hands-on experience in analytical methodologies for biophysical characterization. Hands on experience in Phage or Yeast Display technology for optimization. Experience in working in a BL-2 environment. 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. Imagine what you could do at Novartis!Division NIBR Business Unit BIOLOGICS 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 336942BR Jan 21, 2022 Switzerland Job Description Do you want to be at the forefront of the fight against multiple diseases making an impactful contribution in bringing transformative therapies to patients and be part of Novartis’ mission to reimagine medicine to improve and extend people’s lives? PK Sciences (PKS) offers you this opportunity to make an impact, where 450 projects are straddling discovery through development. PKS is a global organization of about 300 associates, situated within Translational Medicine (TM), in Novartis Institutes of Biomedical Research (NIBR). It is an enterprise organization, unique within pharmaceutical industry, where one can work across both NIBR (Research) and the Global Drug Development (GDD) organizations to apply the scientific knowledge of pharmacokinetics, pharmacodynamics, metabolism and clinical pharmacology in advancing the drug candidates from discovery and clinical development through approval and beyond. Novartis portfolio consists of projects using several therapeutic modalities including small molecules, biologics, gene therapy and cell-based therapies. We are active in multiple therapy areas like Oncology, Autoimmune Diseases, Neuroscience, Musculoskeletal Diseases, Ophthalmology, Respiratory, Cardio-metabolic and Infectious diseases. We collaborate across scientific and organizational boundaries, with a focus on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. In this role of Director/Associate Director PK/PD, you will collaborate with business partners in a cross-functional team to select and characterize new chemical entities and large molecules from research and advance promising entities into the clinic. This unique role will provide matrix leadership to collaborate, align and influence across the cross-functional teams of medical experts, study leaders, pharmacokineticists, statisticians, pharmacometricians and outsourcing experts to identify and mitigate key project issues across therapy areas and implement strategies related to the pharmacokinetic sciences [PKS] discipline (PK, PK/PD, metabolism and clinical pharmacology). Major Accountabilities Include: • Representing the PK/PD/ADME and Clinical Pharmacology discipline, and serving as the primary source of scientific expertise on global cross-functional project teams, leading the design, execution and analysis of PKS preclinical and clinical studies, with focus on moving candidates from the discovery phase to clinics. • Working with subject matter experts in PKS and partner groups, supporting the efficient application and integration of modeling and simulation tools to advance lead optimization and clinical candidate selection. • Making use of PKS resources across NIBR organizations to drive project efforts; ensuring an aligned position on research strategy and in particular human PK/PD and dose projections as candidates transition into the clinic. • Supporting PKS components of preclinical and clinical study protocol designs, preclinical and clinical study reports and investigator brochures, regulatory submission documents, etc. Preparing for Health Authority calls/meetings/discussions and acting as responsible PKS representative in these settings. • Collaborating with other NIBR and GDD functions, bringing innovative ideas and approaches, and a leadership, enterprise mindset that informs and influences the overall drug discovery and development process. 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 • PhD, PharmD or MD in pharmacology/physiology, biochemistry, chemistry, pharmacokinetics/pharmaceutical sciences, or related sciences • Extensive and in-depth knowledge of the drug discovery and/or development process, with a minimum of 10 years’ industry experience in a drug discovery and/or development setting, • Demonstrated success of working in a global matrix environment and with cross functional project teams • Extensive and in-depth knowledge of pharmacokinetics, clinical pharmacology including, drug metabolism and PK/PD evaluation, experience in working in project teams (preferably global) as well as sound awareness of recent developments in drug development and regulatory sciences • Familiarity with standard ADME/PK modelling tools such as Phoenix, GastroPlus, etc. • Experience in authoring regulatory documents with knowledge of global regulatory requirements and guidance is advantageous • Hands-on project experience with low molecular weight and biologics modalities • Strong coaching, mentoring or people management skills are desired • Ability to evaluate in-licensing opportunities and carry out Due Diligence activities as required. • Excellent written and oral (English) communication and negotiation skills Desirable skills: • Hands-on project experience with cell-based and/or gene-based therapies is desirable 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 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 336944BR Jan 21, 2022 Switzerland Job Description Do you want to be at the forefront of the fight against multiple diseases making an impactful contribution in bringing transformative therapies to patients and be part of Novartis’ mission to reimagine medicine to improve and extend people’s lives? PK Sciences (PKS) offers you this unique opportunity to make an impact where 450 projects are straddling discovery through development. PKS is a global organization of about 300 associates, within the Translational Medicine (TM) department, in Novartis Institutes of Biomedical Research (NIBR). It is an enterprise organization, unique to pharmaceutical industry, where you can work across both NIBR (Research) and the Global Drug Development (GDD) organizations to advance the scientific knowledge of pharmacokinetics, pharmacodynamics, metabolism and clinical pharmacology from discovery through approval and beyond. Novartis portfolio consists of projects in multiple therapeutic areas (Cardiovascular, Metabolic Diseases, Immunology, Hepatology, Dermatology, Oncology, Hematology, Neuroscience, Musculoskeletal Diseases, Respiratory, and Opthamology) using several therapeutic modalities including small molecules, biologics, gene therapy and cell therapy. We collaborate across scientific and organizational boundaries, with a focus on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. In this role of Principal Scientist, you will collaborate with a cross-disciplinary team to select and characterize new chemical and biologic entities in research and development and implement clinical pharmacology strategies in early and late clinical development. You will represent the PK/PD/ADME discipline on discovery and development project teams, and suggest and implement strategies and tactics to advance high-quality entities as part of the overall program(s). Major Accountabilities Include: • The specific accountabilities of the role will be based on the stage of the program (preclinical or clinical) • In this role you will provide matrix leadership to collaborate, align and influence across the cross-functional team to identify and mitigate key project issues related to the pharmacokinetic sciences discipline (PK, PK/PD, metabolism and clinical pharmacology). • You will represent the PK/PD/ADME/Clinical Pharmacology discipline as per project need, and serve providing scientific expertise on global cross-functional project teams, leading the strategy, design, execution, and analysis of PKS preclinical and clinical studies. • Working with subject matter experts in PKS and partner groups • Support PKS components of preclinical and clinical study protocol designs, preclinical and clinical study reports, and investigator brochures, IND, NDA etc. Prepare for Health Authority calls/meetings/discussion and be responsible as PKS representative in these settings. • Collaborate with other NIBR and GDD functions, bring innovative ideas and approaches, and a leadership, enterprise mindset that inform and influence the overall drug discovery and development process. • Responsible for the compilation, seeking of approval and updating of Line Function specific elements of development plans to support the TPP (Target Product Profile). • Evaluate in-licensing opportunities and carry out Due Diligence activities as required. Based on binding Swiss work permit regulations, this position can only be offered to an applicant that already has an EU/EFTA or Swiss Passport, or a non-EU/EFTA national that already has an unrestricted Swiss Residence & Work Permit or family reunification ”B permit”. 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 • PhD/PharmD in pharmacology/physiology, biochemistry, chemistry, pharmacokinetics/pharmaceutical sciences, or related sciences. • Preferably 1-3 years of experience in pharmaceutical industry in a field related to PKS (e.g. Drug Metabolism and Pharmacokinetics). • Familiarity with standard ADME/PK modelling tools such as Phoenix, GastroPlus, etc. is desirable • Hands-on project experience with low molecular weight and biologics modalities desirable; and cell-based and/or gene-based therapies highly desirable. • Proven record as team player/leader with superior communication skills. • Demonstrated success working in a matrix environment. • Excellent written and oral (English) communication skills is a must 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 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 353891BR Sep 28, 2022 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. 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! 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 347574BR Jul 19, 2022 Switzerland Job Description Process Expert, Novartis, Basel, Switzerland 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. Our Biotechnology Drug Substance Technology Platform includes 6 Drug Substance sites supplying new biologics entities and biosimilars. Process Expert provides front line technical and scientific expert support for all process-specific issues to ensure execution of processes on-time (business continuity); in compliance to cGMPs, Standard Operations Procedures and applicable guidelines and functional standards and to allow continuously improving in quality, productivity and efficiency. This role is currently limited until end of 2024. Your key responsibilities: Your responsibilities include, but are not limited to: • Act as Subject Matter Expert for the product and process. • Ensure the management of all validation, revalidation, qualification, respecting deadlines and current regulations and execute validations when/where needed. • Develop technical and scientific knowledge of Experts and shop floor technicians. • Lead thorough Root Cause Investigation process for major and critical deviations using investigation tools and methodology. • Perform production impact assessment for complex changes change controls (product and asset change controls). • Prepare, support and follow-up of Health authority and internal inspections. • Collaborate with Regulatory Compliance QA for dossier submissions, revisions. • Ensure implementation and maintenance of the quality systems with the site in accordance with corporate and regulatory guidelines. Support & Perform Optimization projects using Six Sigma Methodology and collaborate with MS&T & technical Development teams for transfer & launch for assigned products, ensure product is fit for plant, support scale up & process improvements. 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 is desirable, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent • Biotechnology experience in DSP/USP desirable • Minimum 2 years of experience in GMP manufacturing process support • Good understanding of regulatory requirements across multiple health authorities • Good working knowledge/understanding of manufacturing execution systems ( SAP, or relevant...) • Fluent German and English language knowledge (spoken and written) • Team player with strong team spirit; open for feedback to learn and grow in the role • Good communication skills and potential to adapt to diverse learning styles 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! 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. Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons. 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 Contract Manufacturing Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 353890BR Sep 28, 2022 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. 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! 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 350062BR Aug 17, 2022 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 medical regulatory writing 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? 766 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 352525BR Sep 28, 2022 Switzerland Job Description Senior Scientist I, Cell Line Screening and Development, Novartis, Basel, Switzerland 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. The Cell Line Screening and Development (CLSD) unit, part of the NIBR Biologics Center, operates at the interface of Research and Development. The unit provides crucial cellular reagents enabling the discovery of novel Biologics in various formats and also creates the cells from which Biologics are manufactured for clinical trials and the market. Your key responsibilities: Your responsibilities include, but are not limited to: • Generation of recombinant cell lines in various mammalian host cell backgrounds to enable therapeutic protein discovery and development - cell transfection, selection, and monoclonal cell line generation as well as cell line screening for productivity. • Preparation of monoclonal cell banks as precursors for GMP cell banks, including transfer protocol preparations. • Work both in a research and in a GMP-like (“DQP”) cell biology environment. • Small scale expression testing by transient transfection of mammalian cells with subsequent analysis using Western Blot, ELISA, flow cytometry and/or other assays • Reporting results using electronic lab notebooks and databases in a timely manner. • Interactions with Biologics Research & Development project teams and presentation of results in team meetings. • Laboratory equipment maintenance. 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: • Background in biotechnology, cell biology, and/or Biologics drug discovery (BSc, MS or apprenticeship with 3+ years of professional experience) • Strong technical expertise in aseptic mammalian cell cultivation (small- and mid-scale) and recombinant cell line generation in various mammalian host cell types (human, rodent cells). • Strong background in cell and molecular biology. • Fluency in English is mandatory, German is a plus. • Strong team player attitude with excellent communication & interpersonal skills and capable of working semi-independently and as part of a cross-functional team. • Background in recombinant protein expression in mammalian cells. • Technical expertise in flow-cytometric analysis of cell populations Desirable requirements: • Technical expertise with FACS-based single cell sorting of mammalian cells • Independent planning and execution of experiments as well as analysis of results. 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! 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. Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons. 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 BIOLOGICS 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 353219BR Sep 26, 2022 Switzerland Job Description Lab Technician/ QC Analyst, Novartis, Basel, Switzerland 50! this is the number of commercial products and late-phase development projects analyzed at BDSS QC Bioanalytics as centralized service lab for the entire Novartis Biotechnology network. Applied analytical techniques are mainly cell-based potency assays for bioactivity determination and ELISA / qPCR for the determination of process-related impurities (e.g. host-cell proteins (HCP), residual Protein A, residual DNA). We are looking for a motivated associate scientist to perform bioanalytical experiments (i.e. cell-based bioassays, ELISA and Q-PCR) for quality control (release, stability, and in-process control (IPC) testing) of biotech drug substances (DS) and drug products (DP) in collaboration with members of the own and cross-functional teams in a cGMP environment. Analytical method validation will be also part of the position. This role is limited for 12 months. Your key responsibilities: Your responsibilities include, but are not limited to: • Planning and performing analytical experiments in a cGMP environment for release-, stability-, and in-process control (IPC) testing of drug substance and drug product samples (e.g. monoclonal antibody) • Check of data and documentation, trending of results and assay performance parameters • Validation and transfer of test methods • As instrument responsible person, perform the evaluation, initial qualification and the periodic functional testing of analytical instruments in accordance with cGMP • Interacting with other groups within Novartis, e.g. the Development department or the respective production sites 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 of 3 years experience as Lab Technician (or 1-4 years for BSc) • Good knowledge of cGMP • Good scientific or technical knowledge in cell-based bioassays, cell culture, ELISA and Q-PCR • Awareness for safe handling of chemicals, cell lines (BL1, BL2), potentially dangerous materials and equipment • Adequate knowledge of software and computer tools and basic presentation skills • Fluent in writing and speaking in English and German language 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! 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. Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons. 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 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 352447BR Sep 26, 2022 Switzerland Job Description Do you want to be at the forefront of the fight against multiple diseases, make an impactful contribution by bringing transformative therapies to patients and be part of Novartis’ mission to reimagine medicine to improve and extend people’s lives? The Pharmacometrics community at Novartis comprises a group of about 80 quantitative scientists supporting a portfolio of more than 80 clinical development projects in 10 therapeutic areas every day. Quantitative sciences are a critical part of bringing these new medicines to patients. Pharmacometrics Scientists bring innovative modeling and simulation skills to every aspect of clinical drug development over a wide range of disease areas and drug modalities. We are dedicated to creating a collaborative and supportive culture where teamwork and learning is emphasized and innovative problem solving is encouraged. Come and join an industry leader where you will have the opportunity to grow and contribute as a quantitative drug development scientist in early- and late-stage projects. The Senior Principal / Principal Pharmacometrics Scientist leads the planning, execution, and delivery of Pharmacometrics strategy on clinical projects within (early/full) clinical development. In this role, you will be responsible for the discussion and implementation of Pharmacometrics methodologies that successfully address the Novartis Institutes for Biomedical Research (NIBR) and Global Drug Development (GDD) objectives on the assigned projects. You will provide Pharmacometrics support for regulatory submissions and supply to drug development decisions with internal and external partners and work with experienced pharmacometricians to collaborate with cross-functional international teams to develop quantitative strategies and will also have the opportunity to explore innovative pharmacometrics methodologies that optimally address the research and development objectives. Your responsibilities include, but are not limited to: • Providing exploratory data and modeling analyses for clinical projects • Contextualizing the modeling question with the relevance to drug and disease biology • Developing an understanding of drug development applied to scoping relevant questions for Pharmacometrics analysis • Helping colleagues with review and validation of programs and outputs • Communication of modeling to project teams in multiple settings such as decision board meetings, small sub-teams, etc. • Training in good clinical practice for data handling and analysis • Learning and developing new quantitative analysis methods and application to practical situations in drug development • Developing posters, publications, presentations for internal and external conferences 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: • Ph.D. in Pharmacology, Biology, Engineering, Mathematics, Statistics, or a field with significant modeling-related content (or equivalent) with 2+ years modeling related activity in mathematical /statistical modeling with strong working knowledge / experience with R / MATLAB / NONMEM / Monolix. Prior pharmacometric experience is not required. *We will hire at Principal or Senior Principal level depending on the experience of the successful candidate. • Proven ability for innovative problem solving, strong fundamentals in mathematical modeling, collaboration skills across functional areas and good communication skills to both quantitative and non -quantitative scientists. *We will hire at Principal or Senior Principal level pending on the experience of the successful candidate. **Some restrictions to flexible working models may apply and will be discussed at interview if applicable Why Novartis? 766 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 CD&A 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 351751BR Sep 26, 2022 Switzerland Job Description 9 Billion! The amount Novartis invests in Research & Development. Novartis Institutes for BioMedical Research (NIBR) is the innovation engine of Novartis, where 5,600 people dedicated to drug discovery harvest the power of new technologies to produce therapeutic breakthroughs to patients. Their efforts are organized in hundreds of research and early development projects that provide reach source of portfolio data, from exploratory to clinical proof-of-concept. We at Portfolio Forecasting, Analytics and Reporting team aim to unlock the potential of this data to support senior management boards in enterprise-wide portfolio decision making. As the Associate Director, Portfolio Data Science and Advanced Analytics – you will be responsible for establishing industry-leading portfolio simulation and advanced analytics methodologies for NIBR research and early development (R&ED) pipeline. This role brings deep technical expertise in statistics, predictive analytics and modelling to lead the development of portfolio forecasting, optimization and information intelligence capabilities within NIBR. The other key purpose of the role will be to apply advanced analytical methodologies in close collaboration with Disease Areas, Global Platforms, Portfolio Strategy Directors, Project Management and Project Teams, to support significant business decisions for R&ED pipeline. The role will also act as an expert thought leader in portfolio data science and advanced analytics. Your responsibilities will include: • Design and lead the establishment of industry-leading portfolio simulation and advanced portfolio analytics capabilities to support senior management boards in their decision-making process to advance our R&ED pipeline. • Provide support to business decisions that have significant impact on our pipeline by applying innovative/quantitative analytical and modeling approaches and collaborating with Project Teams / Project Management, and Disease Areas / Global Platforms to enable actionable recommendations to senior management boards. • Lead cross-divisional portfolio simulation and analysis with an objective to align, shape and connect current NIBR portfolio simulation systems and analysis capabilities to deliver a complete and consistent integrated view of global drug R&D projects, marketed products and new opportunities across Novartis in close collaboration with S&G, GDD, Commercial and Corporate. • Develop and establish advanced portfolio concepts, methodologies and metrics in collaboration with portfolio functions within Disease Areas and across the enterprise, integrating latest AI and digital analytics. • Enable and empower major stakeholders to solve relevant business questions by applying developed analytical and forecasting tools. • Act as an expert thought leader in portfolio theory, data science and data analytics, establishing state-of-the-art methodologies and capabilities for portfolio management across Novartis. Please note this role can be based in Basel Switzerland, Cambridge/East Hanover US or Hyderabad India. Relocation between Novartis sites is not considered. 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: • Science/engineering/data science degree (Master, PhD) or business degree (MBA) required; degrees in at least two fields highly desirable. • Minimum of 10 years of professional experience in the pharma / biotech industry, of which at least 5 years preferably in R&D setting. • Strong multi-disciplinary background with previous experience and deep understanding of R&D portfolio management, decision science, data science, data analytics and statistics. • Technical skills required: data wrangling; descriptive and inferential statistics; trend analysis; agent-based modelling; forecasting and simulation; single and multi-objective optimization; data visualization (R Shiny is a plus); basic machine learning expertise; SQL, R, and python; experience with Git and Bitbucket. • Deep understanding of drug discovery and/or development process. Track record of impact on drug discovery and/or development pipeline. • Proven ability to quickly understand complex abstract technical ideas and concepts, translate them into simple and effective solutions and communicate them effectively to non-technical audiences. • Track record of innovation by transforming the way to solve the problem using data science and artificial intelligence. • Analytical and strategic thinker and problem-solver. • Strong cross-functional matrix leadership experience with proven track record of leading inter-disciplinary internal and external project teams to solve critical business problems. Able to establish strong partnerships without formal authority, strong team player. • Strong planning and organization skills, project management skills, process orientation. • Strong mentoring and coaching skills. Why consider Novartis? 750 million. That’s how many lives our products touch. 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 PORTFOLIO MANAGEMENT - NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Alternative Location 2 India Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 349022BR Aug 01, 2022 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. The Pre-Clinical Safety (PCS) group in NIBR provides world class preclinical safety profiling and assessment for optimal drug discovery, development and commercialization, with state-of-the-art regulatory compliance. As a molecular and computational safety scientist, you will be involved in a wide range of projects within the Genome Safety section at Novartis, Preclinical Safety (PCS) department. In this role you will collaborate with multi-disciplinary scientists to support the safety of LMW compounds and Cell & Gene Therapy products within the Novartis Research and Development portfolio. You will develop and apply a broad range of molecular biology and bioinformatic techniques and perform high quality experiments and procedures with a high degree of technical and scientific autonomy. With your biocomputational background, you will also contribute to the qualification, analysis, integration, and interpretation of the results generated, including next-generation sequencing data from internal and external data sources. You have a deep understanding of biological questions and a pro-active attitude towards your cross-disciplinary collaborators (biologists, toxicologists, computational scientists, drug discovery 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 Required skills:  Master’s degree or equivalent with work experience in molecular and computational biology as well as experience working in genome editing or viral research projects within academic and/or drug discovery settings.  Hands-on experience with molecular biology and biochemistry techniques (nucleic acid extraction, PCR, ddPCR / qPCR, western blot, cloning, cell culture). Prior experience in cytogenetics, viral integration site analysis, CRISPR off-target, library prep for NGS, chromosome conformation capture (3C, 4C, HiC) and/or rapid amplification of cDNA ends (RACE) is a plus.  Confidence working in a UNIX environment. Experienced with next generation sequencing data analysis and biostatistics. Solid programming skills in R or Python and/or previous experience in viral integration site analysis or CRISPR off-target is a plus.  Collaborative, flexible, critical thinking and strong team player.  Excellent organization and communication skills, independent, organized, and accurate working style, committed to high quality.  Fluent English (written and spoken) This role can be based in either Basel, Switzerland or Cambridge Mass. US. 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/networkDivision NIBR Business Unit Translational Medicine 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 347805BR Jul 18, 2022 Switzerland Job Description QC Analyst Microbiology II, Novartis, Basel, Switzerland Unser globales Produktions- und Liefernetzwerk arbeitet 365 Tage im Jahr, um sicherzustellen, dass unsere Patienten die Behandlungen erhalten, die sie für ein längeres und gesünderes Leben benötigen. In dieser Position würden Sie verantwortlich für eine Selbständige, GMP-konforme und termingerechte Durchführung, Auswertung und Dokumentation aller zugewiesenen im Labor anfallenden Arbeiten unter Einhaltung der Analysenvorschriften, SOP's und Sicherheitsrichtlinien. Eigenverantwortung für die Prozesse innerhalb der Laborgruppe und Sorgfalt für die ihm zugeteilte Arbeiten und Gerätschaften sein. Diese Position is gesucht für 1 Jahr. Zu Ihren Aufgaben gehören unter anderem: • Selbständige, Durchführung, Auswertung, Dokumentation und Interpretation von Routineanalysen im Bereich der mikrobiologischen Analytik (z.B. MET, BAN etc.). Löst auftretende Probleme vorwiegend selbstständig • Einhaltung von Terminvorgaben und rechtzeitige Information an Vorgesetzte im Fall von absehbaren Verzögerungen und Problemen • Einhaltung der GMP- und Arbeitssicherheitsvorschriften Pflege, Betrieb und Unterhalt der Geräte und Einrichtungen • Unterstützung des Teams bei Laboruntersuchungen und Problemlösungsfindungen • Selbständige Erstellung von Berichten (z.B. OOS) • Mitarbeit in Projekten 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: • Ausbildung als Biologie-Laborant • Kenntnisse in der MET Analytik sowie über Mikroorganismen und der Umgang mit denselben (aseptisches Arbeiten) sind Voraussetzung • Mindestens 3 Jahre Erfahrung in einem Mikrobiologielabor (zusätzlich zur Lehrzeit), fundierte Erfahrung in Qualitätskontrolle • GMP Erfahrung • Besitzt vertiefte Kenntnisse in allen gängigen Laborrelevanten Techniken (Plattenguss, Filtration, Ausstrich) • Gute Kommunikations- und Teamfähigkeiten • Fliessendes Deutsch in Wort und Schrift / Englisch von Vorteil • IT: Gute Computerkenntnisse, Office-Anwendungen, SAP, LIMS 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 NTO 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 353503BR Sep 23, 2022 Switzerland Job Description Research Scientist Protein Physicalchemical Characterization(80-100%*), Novartis, Basel, Switzerland 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. NIBR Biologics Center (NBC) is responsible to create new Biologics entities ranging from monoclonal antibodies to AAV molecules, and to ensure their fitness to the development journey. To fulfill the purpose, we aim to develop and implement state of art analytical capabilities in particular physicalchemical analytics for quality control and characterization. Today, we are looking for a motivated scientist who will apply the existing and/or new biophysical analytical methods to the characterization of next generation biologics. This role is limited for 10 months Your key responsibilities: Your responsibilities include, but are not limited to: • Develop and perform of physico-chemical characterization of biologics product using state-of-the-art equipment, incl. Capillary gel electrophoresis, capillary isoelectric focusing, dynamic light scattering and various biophysical techniques. • Explore new biophysical technologies for the characterization of next generation biologics, for example, mass photometry, FT-IR, SEC-MALS and automated western blotting. • Interpret data and summarize the result in an analytical report. • Schedule and perform routine maintenance of lab instruments/equipment, organize the general lab infrastructure (e.g., consumable orders) • Write laboratory protocols, present the outcome to the analytical community. 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 or equivalent education in Analytical chemistry, Biochemistry, Biotechnology or a related discipline. • Practical experience in one or several PhysChem analytical techniques, such as capillary electrophoresis, capillary isoelectric focusing, dynamic light scattering, or various biophysical techniques. • Working experience in academic research environment is of advantage. • Solid theoretical understanding of protein chemistry and analytical methods for biophysical characterization of proteins. • Proficiency in English (oral and written), German and/or French would be helpful. • Capability to perform and interact with a global multi-disciplinary team; Curious to learn and develop into new scientific areas. • Diligent and accurate working style, excellent communication and organizational skills are required. Desirable requirements: • Knowledge of mass photometry, FT-IR, SEC-MALS or automated western blotting is a plus; • Curious to learn and develop into new scientific areas. 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! 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. Novartis are an equal opportunities employer and welcome applications from all suitably qualified persons. 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 BIOLOGICS NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Temporary Shift Work No Apply to JobAccess Job Account

Job ID 353610BR Sep 23, 2022 Switzerland Job Description 18! That’s the number of months that you will be spending in Chemical and Analytical Development (CHAD) department enrolled as a Postdoc working in the Biocatalysis Team. We are looking for highly motivated talents who recently completed their PhD to support and further expand use of biocatalysis technologies in Pharmaceutical Industry. This Postdoc position is a unique opportunity to work in the field of applied biocatalysis sciences in the Pharmaceutical industry with exposure to cutting-edge technologies at the interface between research and development. In alignment with Novartis ambition to become a global leader in environmental sustainability, the candidate will have the chance to positively impact the carbon footprint of Novartis. The candidate will not only be able to transfer know-how into practice, but also to develop soft skills and grow internal network for a future career in the Pharmaceutical industry. Start date: January 2023 Duration: 18 months Your responsibilities: Your responsibilities include, but are not limited to: • Develop biocatalytic processes on relevant projects within Novartis portfolio across different scales. • Be part of the Biocatalysis / Protein engineering team to develop and optimize enzymes used in process R&D. • Develop efficient biocatalytic processes for the synthesis of oligonucleotides. • Investigate various enzymatic approaches for oligonucleotide bioconjugation and evaluate their potential by applying cutting-edge robotic platforms for high-throughput screenings. • Collaborate with diverse experts in the areas of Molecular Biology, Biochemistry, Analytics, Bioinformatics, Process Chemistry and Process Engineering. #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: • Completed PhD, preferrably at the interface of Chemistry and Biology and ideally with a focus on Biocatalysis. • Experience in enzyme engineering and biocatalytic process development is a strong plus • Expertise in either oligonucleotide, peptide or protein modifying enzymes is preferred • An excellent track record of original research and extensive experience in developing biocatalytic transformations using “state of the art” technologies • Fluency in English required; additional German proficiency is a plus • Ready to expand own knowledge, open minded with an international outlook • Finally, since all work takes place in multidisciplinary project teams, strong interpersonal and communication skills are required 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 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 344776BR Jul 25, 2022 Switzerland Job Description 1 out of 10 people are suffering from immunological diseases. The Autoimmunity, Transplantation & Inflammation (ATI) 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, ATI is seeking an innovative and highly motivated Principal Scientist or Senior Principal Scientist to initiate and guide research approaches in the area of Immune Tolerance. You will be responsible for leading a state-of-the-art laboratory of experienced scientists to discover and develop novel therapies aiming at restoring tolerance in various autoimmune and inflammatory diseases. This will include the use of in vitro assays and in vivo models to evaluate innovative therapeutic approaches with potential for long-term impact on the disease course. The ideal candidate will hold a PhD and have an in-depth research and industry background in Immunology. Your responsibilities will include but not limited to: • 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: • PhD degree in immunology, autoimmunity, immuno-oncology or related Immunology field • In-depth knowledge of human and mouse immunology, mechanisms of tolerance induction and cell populations with immunoregulatory properties • Experience in cutting-edge novel therapeutic approaches (e.g. gene-, RNA/DNA- or cell-therapy, complex biologics modalities, etc) • Significant scientific accomplishments and successful collaborations documented by publications in high-impact journals • Excellent organization, communication, presentation and analytical skills Desirable requirements: • PhD + a minimum of 5 years of relevant research experience in an academic setting and/or in the pharmaceutical/biotech sector with a focus on Immunology and Autoimmunity • Proven experience in independently working on projects dissecting immunological pathways in health and disease, or evaluating innovative therapeutic strategies for efficacious and durable treatment of immune-mediated pathologies 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 new technologies. 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. We are Novartis. Join us and help us reimagine medicine. * 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 352378BR Oct 04, 2022 Switzerland Job Description Als Logistics Expert werden Sie die Logistik und deren zugewiesenen Prozesse im jeweiligen Bereich (Inbound-, Outbound-, Produktionslogistik) und Projekte zur deren Weiterentwicklung und Optimierung unterstuetzen. Ihre Hauptaufgaben: GROWTH / EFFICIENCY • Definiert in Zusammenarbeit mit dem jeweiligen Head, misst und überwacht die entsprechenden Kennzahlen in seinem Bereich • Erstellt Problem- und Ursachenanalysen bei Prozessabweichungen / Nichterreichung von Zielen und entwickelt Massnahmen zu deren Behebung • Leitet Projekte zur Erhöhung der Effizienz und Optimierung der Prozesse • Ist Ansprechpartner für Stakeholders (POCH, Pharma Supply Chain, ChemOps und CPO’s) der zugewiesenen Prozesse • Unterstützt aktiv eine nach LEAN und 6S Kriterien ausgerichtete Arbeits- und Produktionsweise QUALITY / SAFETY • Bearbeitet / Eröffnet die Abweichungen (Deviations / Complaints) in seinem Bereich und sorgt für die termingerechte Umsetzung der entsprechenden Korrektivmassnahmen • Setzt Massnahmen aus den entsprechenden Abweichungen und Audits unter Anleitung um und stellt deren Nachhaltigkeit sicher • Ist für die Umsetzung der „First-Time-Right“ Kultur in seinem Bereich verantwortlich • Mitverantwortlich für eine Sicherheitskultur (Behavior Based Safety – BBS) in seinem Bereich und für die Einhaltung der geltenden Sicherheits- und Hygienevorschriften. • Führt Auditrundgänge in seinem Bereich durch und ist SME für diesen. PEOPLE • Unterstützt den Head seines Bereiches in der Personalplanung • Sorgt für eine selbstverantwortliche offene Art der Zusammenarbeit und Kommunikation • Ist Vorbild für die Organisation im Bereich der Novartis Values & Behaviors • Unterstützt und / oder vertritt die SD Logistics in übergreifenden sowie fachtechnischen Gremien 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 • Abgeschlossene Lehre im technischen Bereich mit Vorteil aus dem Bereich der Logistik sowie einer Weiterbildung auf Stufe HF / FH. • Deutsch / Englisch in Wort und SchriftDivision Novartis Technical Operations Business Unit NTO 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 351102BR Sep 19, 2022 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. An AS&T Analyst assists AS&T (Analytical Sciences & Technology) laboratory areas in the execution of analysis in the frame of the microbiological control of our production environment and products including project support, and project implementation and performs AS&T technical writing for updates to Standard Operating Procedures (SOPs). Your key responsibilities include, but are not limited to: - Evaluation, validation, introduction and transfer of new microbiological test procedures incl. alternative methods. - Optimization and validation of microbiological analytical methods and equipment as well as cooperation on pharmacopoeial issues. - Evaluation of the efficacy of disinfectants and disinfection procedures by means of suspension and microbe carrier tests. - Support production departments regarding the qualification and re-qualification of H202- treatment procedures (isolators, locks) as well as of E-beam decontamination procedures in time and in accordance to cGMP rules, QMs and SOPs. - Determination of standing times for liquid bulk for sterile drug products, holding times for aqueous intermediates for non-sterile drug products and drug products after reconstruction. - Support of the production department's in qualification and re-qualification of sterilizers and stopper washing equipment by preparation and evaluation of Bi's and EPl's. - Guarantee the maintenance of the QC MICROBIOLOGY culture collection (cryo cultures of official test strains and of in-house organisms). - Assurance of GMP compliance in the laboratory. - Adherence to the safety and ecology guidelines. - Archiving documents of the team, according to the requirements of the relevant SOP. Please not that this is a temporary position limited to 24 months. 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 - (Technical) university diploma or very experienced laboratory technician in biology, biochemistry or pharmacy or equivalent. - Fluent in spoken and written German and good knowledge of English. - Experience in biological/microbiological analytics or diagnostics and/or quality control in pharmaceutical industry or biotechnology. - Experience in Equipment Qualification. - Knowledge in pharmaceutical manufacturing, incl. preparation, use and production of sterile drug products. - Skilled in communication to team members, peers as well as to customers. 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! Novartis is an equal opportunities employer and welcomes applications from all suitably qualified persons. 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 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 353008BR Oct 04, 2022 Switzerland Job Description 80 Millionen! Diese Anzahl an Fertigspritzen, Vials und Ampullen werden jedes Jahr in den Steriles im Werk Stein hergestellt und als Medikamente in mehr als 150 Ländern geliefert. Für das Engineering Team suchen wir per sofort ein/e motivierte/n und engagierte/n Praktikanten/in für 12 Monate, welche/r einen Einblick in den Bereich des Betriebsengineerings erhalten und uns aktiv unterstützen wird. Präferiertes Startdatum: Januar 2023 Dauer: 12 Monate Aufgaben: • Mitwirken bei der Planung und Umsetzung von Investitionsprojekten • Durchführung und Betreuung kleinere Projekte im technischen GMP- sowie GSU-Umfeld • Selbstständige bzw. Unterstützung bei der Vorbereitung und Durchführung von Commissioning-, Qualifizierungs- und Validierungsaktivitäten • Mithilfe bei der Vorbereitung und Bearbeitung von Risiko- und Gefährungsanalysen und Änderungsanträge (Change Request) • Unterstützung im Bereich Data Integrity Remediation Plan • Identifikation von Prozessschwachstellen und Mithilfe bei Projekten zur Prozessverbesserung • Erstellung und Überarbeitung spezifischer Betriebsanweisungen und Checklisten basierend auf dem Novartis Manufacturing Manual #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 Anforderungen: • abgeschlossenes Bachelor/Masterstudium im technischen Bereich (mit Abschluss vor max. 12 Monaten) • Gute Englisch- und Deutschkenntnisse • Teamfähigkeit und Flexibilität • Offene Kommunikation und Engagement Warum Novartis? 766 Millionen - so viele Menschen haben wir mit unseren Produkten im Jahr 2021 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. Wir sind Novartis. Kommen Sie zu uns und erfinden Sie Medizin mit uns neu.Division Novartis Technical Operations Business Unit NTO 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 351224BR Aug 22, 2022 Switzerland Job Description 28,000! associates of more than 100! nationalities deliver high quality and affordable medicine on time, every time, safely and efficiently. If you want to be part of this then join us now and be part of a team of highly skilled & experienced laboratory professionals who contribute by performing analytical release testing, investigational support, research support, and stability testing. Your main responsibilities will entail: • OOx/Deviation handling • CAPA definition • Ensure all activities in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) • Stability testing (Projects) – protocol preparation, evaluation, report preparation . • Reporting (stability plan preparation, trend analysis, evaluation) • Performance of stability studies, protocols and comparative reports for supplier qualification • Review and approval of analytical tests (analytical release) • Microbiological QC -Perform microbiological testing of materials and utilities, environmental & personnel monitoring -Provide expert support for site qualification & validation activities 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 • 3-5years experience in Pharma/Manufacturing sector in analytical lab in a GMP environment • Laboratory Excellence • Quality Control (QC) Testing Quality/ Control Sampling • Quality decision making • Knowledge of IT Applications & tools • Knowledge of TQM and related industry • GxP standards and processes 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 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 351845BR Sep 19, 2022 Switzerland Job Description 25000+! The total no of associates in NTO who deliver high quality, affordable medicines on time, every time, safely and efficiently. We strive to become the top manufacturer of innovative and generic medicines in the industry - while keeping our patients at the heart of everything we do The Shift Leader is responsible for managing his/her team to carry out the manufacturing operations according to schedule in compliance with HSE and GMP rules. Main duties: People Management: • Represent production management to the team members and promote Novartis values within the team • Lead the TIER1 process and report status to other stakeholders • Line responsibility and shift walkthrough • Engage and motivate the team and delivers strong results with an empowered team • Ensure responsibility for the quality of the work and the associated documentation Coordination & Problem Solving: • Translate operational schedule into team activities. Optimize the use of technical resources to reach daily goals • Ensure the distribution, documentation, centralization, control and then transmission of production documents • Ensure the proper documentation and management of the logbooks • Ensure the adjustment of the production schedule in connection with the Operational scheduler and the • updating of KPIs Quality: • Promote and improve the Quality culture • Facilitate / Coordinate, in collaboration with Quality Assurance, the upgrading, and the improvement of Quality by verifying the practical application on the shop floor • Ensure overall inspection readiness for area of responsibility HSE: • Supervision, incident reporting and action follow-up at shop floor level • Ensures compliance with safety, cleanliness and tidiness rules (housekeeping, 5S) • Promote and improve the HSE culture, by implementing the necessary systems and actions in line with the evolution of the site Continuous Improvement: • Manage the process of continuous improvement at the workshop level by fostering innovation and initiatives through actions on shop floor • Manage / participate in continuous improvement projects in line with strategic objectives and ensure communication and involvement of technicians and support 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 • Minimum 5 year experience in chemistry / food / pharmaceuticals / biotech / aseptic manufacturing or development • Min. 2 year experience in a coordination role in GMP environment Languages: Fluency in German, intermediate EnglishDivision Novartis Technical Operations Business Unit NTO 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 353031BR Sep 21, 2022 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. Um die Abteilung Novartis Technical Operations zu verstärken, suchen wir per sofort 1 Prozessmitarbeiter(-in) im Bereich der Fertigspritzenabfüllung (Isolatortechnologie) mit Schichtbereitschaft. 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 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 • Isolator oder Reinraum-Qualifizierung • Beherrscht die Technologien im Bereich der Abfüllung (e.g. e-Beam, Isolator und FVA - Füllverschliessanlage) • Abgeschlossene Berufslehre als Chemie- und Pharmatechnologe oder ähnliches oder langjährige, einschlägige Berufserfahrung in der Chemie- oder Pharmabranche • Train-The-Trainer Ausbildung • Sehr gute Deutschkenntnisse in Wort und Schrift. Englischkenntnisse sind gewünscht. • Motivation, Flexibilität und Team Fähigkeit Affinität für digitale Technologie • MES/PAS-X Erfahrung • SAP und PMX Erfahrung Warum Novartis? Ueber 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. 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 NTO 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 349906BR Aug 05, 2022 Switzerland Job Description 80million! This is the number of products that are processed in our Production Site in Stein per year. As part of our Quality Control team, you will play a key role in analyzing and confirming the highest product quality for millions of patients in more than 150 countries around the world. We are looking for a highly skilled & experienced laboratory professional who will contribute from Day 1 by performing analytical release testing, investigational support, research support, and stability testing. Your main responsibilities: -OOx/Deviation handling -CAPA definition -KPI trending -Ensuring all activities are in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) -Stability testing (Projects) – protocol preparation, evaluation, report preparation . -Reporting (Stability plan preparation, trend analysis, evaluation) -Performance of Stability studies, protocols and comparative reports for supplier qualification -Review and approval of analytical tests (analytical release) -Microbiological QC -Perform Microbiological testing of materials and utilities, environmental & personnel monitoring -Provide expert Support for site qualification & validation activities -Maintain and calibrate equipment incl. plan preparation -Support in supplier qualification -Trending and analysis of KPI/KQI -Support sample planning and sampling execution -Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt -Qualification (IQ/OQ/PQ) of computerized analytical instruments -Project work for the digitization of QC processes 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 - 3-5years experience in Pharma/Manufacturing sector in analytical lab in a GMP environment/equivalent - Quality Control (QC)/ Testing Quality Control Sampling - Quality decision making - Knowledge of IT Applications & tools - Knowledge of TQM and related industry GxP standards and processes -Fluent German, proficiency in English 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. *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 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 No 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 352755BR Sep 14, 2022 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: November 1, 2022 Latest start date: January 2023 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 NTO 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 Sep 15, 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 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 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 352092BR Sep 06, 2022 Switzerland Job Description 1! excellent opportunity to join our organization! We are looking for motivated recent postgraduates who are interested in postgraduate internship opportunities in the near future (coming up in the next months). Duration: 2 years Your responsibilities: • Support front-line manufacturing, focusing on manufacturing each batch safely, on time and in compliance with batch instructions and quality requirements • Support first-line evaluation of product- and process-related issues • Support the assessment and execution of technical changes and process changes • Execute process improvements #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. 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’ll bring to the role: • Education: Bachelor/Master Degree in Engineering, Pharmaceutical Sciences, Life Sciences, Biotechnology and similar; completed within the past ca. 12 months • Languages: English (German a plus but not a must) • No previous industry experience needed 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 NTO CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma Stein Functional Area Technical Operations Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 352826BR Sep 15, 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 we imagining medicine but we are also impacting on, saving and improving quality of life. 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 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 352828BR Sep 15, 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 • Bachelor’s degree or Apprenticeship in relevant Engineering or Scientific discipline (e.g. Biology or Laboratory Assistant) • Minimum of 1 year experience in cGMP or academic or lab setting with aseptic or cell culture experience required • If no degree, a minimum of 2 years’ experience in cGMP or academic or lab setting with aseptic or cell culture experience required • 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 350499BR Sep 15, 2022 Switzerland Job Description 80million! This is the number of products that are processed in our Production Site in Stein per year. As part of our Quality Control team, you will play a key role in analyzing and confirming the highest product quality for millions of patients in more than 150 countries around the world. We are looking for a highly skilled & experienced laboratory professional who will contribute from Day 1 by performing analytical release testing, investigational support, research support, and stability testing. Your main responsibilities: • OOx/Deviation handling • CAPA definition/ KPI trending • Ensuring all activities are in compliance with cGxP, incl. data integrity review and approval of analytical data / tests (analytical release) • Stability testing (Projects) • Review and approval of analytical tests (analytical release) • Microbiological QC/ Perform Microbiological testing of materials and utilities, environmental & personnel monitoring • Provide expert Support for site qualification & validation activities • Maintain and calibrate equipment incl. plan preparation • Support sample planning and sampling execution • Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt • Qualification (IQ/OQ/PQ) of computerized analytical instruments • Project work for the digitization of QC processes 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 • 3-5years experience in Pharma/Manufacturing sector in analytical lab in a GMP environment/equivalent • Quality Control (QC)/ Testing Quality Control Sampling • Quality decision making • Knowledge of IT Applications & tools • Knowledge of TQM and related industry GxP standards and processes • Fluent German, proficiency in English 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. *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 connectedDivision 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 Regular Shift Work No 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 353834BR Sep 28, 2022 Switzerland Job Description 2 Billionen! Diese Anzahl von Tabletten, Kapseln, Ampullen, Fertigspritzen, Fläschchen, Autoinjektoren und transdermalen Therapiesystemen wird jedes Jahr in Stein hergestellt und in mehr als 150 Ländern geliefert. Nehmen Sie an diesem Erfolg teil, indem Sie sich Novartis Stein anschliessen! Als Technician I, Automatiker / Automation Technican sind Sie für die Durchführung von Wartungs-, Kalibrierungs- und Inbetriebnahmetätigkeiten in der Produktion im Verpackungsbereich zuständig. Zu Ihren Hauptaufgaben gehören: • Durchführung von geplanten Instandhaltungsmassnahmen • Fachgerechte Behebung von Anlagenstörungen an automatisierten Inspektions- und Verpackungsanlagen im GMP Umfeld • Qualifizierung und Justierung von Insepktionssystemen • Protokollierung und Rückmeldung der durchgeführten Tätigkeiten im SAP • In Zusammenarbeit mit dem Engineering arbeiten Sie aktiv an der Verbesserung der Anlagenverfügbarkeit und präventiver Instandhaltung • Sie unterstützen Projekte für Neuanlagen sowie Projekte bei Änderung bzw. Verbesserung der bestehenden Anlagen 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 ist notwendig für diese Funktion: • Bildungsabschluss als Automatiker, Elektriker, Mechantroniker oder Energieelektroniker Anlagentechnik mit Berufserfahrung in der Automatisierungstechnik und/oder Maschinenbau • Grundkenntnisse in SPS-Programmierung und Netzwerktechnik • Kenntnisse in SPS PM-Modulen • NIV 13 Betriebselektrikerbewilligung von Vorteil • Vorkenntnisse in Inspektions-Systemen • Bereitschaft für Normalarbeitszeit, 2-Schicht/3-Schicht sowie Pikett-Dienst • Deutsch (fliessend), Englisch (Grundkenntisse) 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 NTO 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 Yes Apply to JobAccess Job Account

Job ID 348850BR Sep 02, 2022 Switzerland Job Description 80Millionen! Das ist die Anzahl der Produkte, die in unserer Produktionsstätte pro Jahr verarbeitet werden. Als Teil unseres Qualitätskontrollteams spielst du eine Schlüsselrolle bei der Analyse und Bestätigung der höchsten Produktqualität für Millionen von Patienten in mehr als 150 Ländern auf der ganzen Welt. Als QC Analyst I wirst du zustaendig für die Erledigung der zugewiesenen Aufgaben im Labor für die Qualitätskontrolle gemäß den cGxP-Vorschriften./ Durchführung von laborspezifischen Tätigkeiten, wie Analysen, Wartung, Kalibrierung und Qualifizierung der Analysegeräte. Hauptverantwortlichkeiten: • Lagerung und Verwaltung von Proben • Sicherstellung aller Aktivitäten in Übereinstimmung mit cGxP, inkl. Datenintegrität • Stabilität (wenn nicht zentralisiert) - Stabilitätsproben gemäß cGxPStandards analytisch dokumentieren 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 • Bevorzugt: Vorerfahrung im Laborumfeld/ als Chemielaborant der Pharmaindustrie (Qualitätssicherheit, Produktion) • Abgeschlossene Ausbildung zum Laborassistenten oder gleichwertige Ausbildung • Fließend Deutsch (mündlich und schriftlich) Grundkenntnisse in Englisch (mündlich und schriftlich) Über 799 Millionen! - so viele Menschen 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 zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. 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/networkDivision 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 No Apply to JobAccess Job Account

Job ID 348578BR Jul 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 a highly motivated QC Analyst II who will execute of assigned tasks in the quality control laboratory in accordance with cGxP regulations and add additional value to our team of professionals. In this role you will ensure orders are processed correctly and quickly, with no waiting times due to wrong or delayed order. You will manage deadline adherence rate: orders completed on time, all missed deadlines reported in good time, the shortest possible lead time, as well as ensure constant readiness for inspection, no critical complaints from superiors and inspectors. You will consistently follow the GMP and GSU guidelines, as well as the SOPs, no critical irregularities and find/implement optimization options to reduce costs. We are looking for you, who will become a role model for the team in terms of values and behaviour and set an example of self-empowerment. Join us! Major responsibilities: • Execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations. • Performance of timely analyses. • Performing of raw data checks • Role model for the team in terms of values & behaviour • Self-empowerment 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 - Completed apprenticeship as a laboratory assistant or equivalent training - Experience on the job: 1-5 years - Self initiative individual - A team player, but also able to work independently *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/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 No Apply to JobAccess Job Account

Job ID 347997BR Sep 12, 2022 USA Job Description 800 biomarker discovery and development projects, across more than 100 clinical studies, which generate 20 petabytes and 2 million patient-years of data! All waiting for you to unlock the next breakthrough in medicine. Biomarkers are critical components of translational research, enabling robust therapeutic and mechanistic hypothesis testing in early clinical development, and as precision medicine enablers e.g. defining patient subpopulations, understanding disease heterogeneity, predicting therapeutic responses, and potential development as diagnostics. As a BMD Therapeutic Area Lead (TAL) you will lead the disease area biomarker matrix team and be responsible for the development and implementation of “fit for purpose” biomarker strategies and providing an effective interface for transitioning projects from early to later stage clinical stages. You will be a core member of Global Biomarker and Diagnostic Teams, engaged in Translational Data Science teams, and provide therapeutic area line function review for clinical protocols. As a TAL you will lead efforts to identify, develop, and drive disease, mechanistic and compound biology that serves the precision medicine approaches for the multi-indication portfolio. In the role of Therapeutic Area Lead in NIBR Biomarker Development (BMD) you will be responsible for: Delivering clinical project and disease biomarker “fit for purpose” biomarker strategies and plans within one or more General Medicine disease indications (Cardiovascular and Metabolism, Hepatology, Renal, or Ophthalmology). • Leading a dedicated matrixed group of biomarker subject matter experts and project team representatives to develop and oversee clinical project strategies, plans and timelines in partnership with line function leaders. • Representing BMD line functions in Therapeutic Area Line Function committees for clinical protocol development • Representing Biomarker Development on Cardiovascular and Metabolism, Hepatology, Renal, or Ophthalmology early and late Disease Area Decision Boards to identify, develop, and drive disease and compound mechanistic biology, and precision medicine approaches for the portfolio.• • Leading strategic translational data working groups centered on integrating and analyzing large-scale patient muti-modal data sets ( omics, imaging, digital, etc.)to identify new indications, endpoints, and responsive patient subpopulations. • Providing thought leadership with other BMD TALs to identify synergies and drive innovation across our large and diverse clinical portfolio. • Implementing strategies in close collaboration with the BMD global organization which includes over 100 associates with expertise in all aspects of biomarker science i.e. genetics, genomics, molecular and cellular, digital devices, imaging and data sciences Vaccine Policy: While Novartis does not require vaccination at this time, for certain Novartis sites in the US all associates and candidates may be required to either upload an image of their COVID-19 vaccine card demonstrating proof of full vaccination for COVID-19 (or other similar evidence of vaccination) or proof of a negative COVID-19 test taken by the associate or candidate within the past seven days to enter any of our sites and/or customer office or healthcare facility, as well as prior to participating in other work related off-site meetings. Employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to [email protected]. 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 will bring to the role: Minimum Requirements: • MD , MD/PhD, or PhD degree required, plus additional PhD/postdoc or equivalent level research • Deep understanding of clinical disease epidemiology that can be applied to questions of diagnosis, biomarker development and treatment monitoring strongly preferred • Scientific excellence supported by recognized high quality publications; clinical and/or biological expertise in cardiovascular and metabolic diseases, hepatology, renal, or ophthalmology (Board certified or similar level preferred) • Experience performing similar role within a pharmaceutical/biotechnology research company, clinical research organization or academic medical center • Significant relevant experience after your MD/PhD/postdoc including quantitative expertise in biostatistics, bioinformatics, computer biology, statistical genetics, clinical imaging, machine learning, or data science; interpreting and publishing studies consisting of “omics” data e.g. genetics, genomics, proteomics; closely partnering with/leading data scientists • Proven success in leading and partnering in multidisciplinary matrix teams across Pharma/biotech (clinical research thru healthcare applications), academic institutions, or commercial business functions • Well-developed interpersonal skills with good presence and ability to influence and negotiate with senior leadership; experienced presenter and communicator • Fluent in oral and written English; other languages e.g. German, French, Italian useful but not required Position can be based in Basel, Switzerland or Cambridge, MA USA. 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.Division NIBR Business Unit Translational Medicine 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 339762BR May 16, 2022 Austria Job Description Technical Transfer Operations Lead (f/m/d), Global Drug Development - Schaftenau, Austria / Basel, Switzerland 150! That’s the number of GDPD projects in development, 100+ medical devices and combination products. This global role has been built to optimize and harmonize device and combination product transfer processes as well as lead LCM of commercial device and combination products. Your key responsibilities: • Provide expertise from the combination product/medical device platform point of view for strategical, process, technical, and e-systems related topics during device development stages, commercialization as well as for commercial products • Establish an aligned technical transfer strategy for GDPD with NTO and harmonize cross-site manufacturing transfers from development to site level • Establish and uphold aligned template based documentation for design transfers to NTO • Coordinate development support of product maintenance operations for NTO as a customer and manage teams to implement changes concerning the medical device platform • Support the Transfer Team lead in Launch Site Decisions and in technical launch activities for assembly and packaging at involved sites and is a member of the GDPD Device Development subteam • Supports the manufacturing representative during device development stages (design control) and in the packaging design process for the GDPD product portfolio. 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: Essential: • PhD, Dipl. Ing. in Mechanical Engineering or Pharmaceutical Technology • Minimum 5 years professional experience in Pharmaceutical Manufacturing (preferably assembly & packaging) with fundamental understanding of standard device/packaging analytical testing. Solid experience in reviewing and writing technical reports • Thorough understanding of product processes and strong working knowledge of applied statistics, quality systems and regulatory requirements across multiple health authorities. • Knowledge in design control, documentation, risk management and processes such as DMR (Device Master Record), DHF (Design History File), pFMEA, Design Verification, and URS (User Requirement Specifications). • Knowledge of 21 CFR part 210/211, 21 CFR part 4/820 and ISO 13485, ISTA, ASTM and EMA medical device directive. • Strong Project management skills. Strong communication and intercultural skills with ability to work in a global matrix environment. • Fluent in English, German is a plus 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! In addition to a market-competitive base salary, we offer an attractive incentive program, a modern company pension scheme, childcare facilities, learning and development options as well as worldwide career opportunities within the Novartis group. In accordance with Austrian law, we are obliged to disclose the minimum salary as stated in the collective bargaining agreement. For this position the minimum salary is € 52.204,04/year (on a full time basis). In most cases, the actual salary will be higher, as we strive to maintain a competitive position in the market and consider your previous experience, qualifications and individual competencies We are open for part-time and job sharing models and support flexible and remote working where possible. 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 Austria Site Schaftenau Company / Legal Entity Sandoz GmbH 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 334811BR Aug 24, 2022 USA Job Description 750 million+. That’s the number lives our products touch. While we’re proud of that fact, in this world of digital and technological transformation, we must continue to improve and extend even more people’s lives. We believe we can achieve the goal when curious, courageous and collaborative people like you are brought together in an inspiring environment, empowering you to take calculated risks, and teaming you with people who share your determination, to tackle the world’s toughest medical challenges. We have an exciting new opportunity for a Director Pharmaceutics to lead strategy for clinical development programs. In this role, you will drive the design and implementation of methodologies that help optimize drug development programs at the Development Unit and/or disease area level and manage a portfolio. You have an opportunity to lead and integrate input from different quantitative scientists impacting clinical development, health authority interactions and represent the PMX function at internal and external decision boards, develop and mentor other pharmacometricians, and provide strategic, technical, operational and scientific leadership and solutions to the organization. What you’ll be doing: • Lead the PMX contributions to the integration of relevant technical and disease area knowledge in the planning and execution of robust development programs. • Represent the development unit internally and externally as the pharmacometrics expert, including regulatory interactions. • Foster the integration of pharmacometric methodology into clinical development programs, and ensure that the Analytics team (biometrician, data management, database programming, programming, medical and scientific writing) are aligned on the pharmacometric strategy, its execution and delivery. • Anticipate needs for PMX and strategic support at the disease/therapeutic area levels. • May manage portfolio at Disease/Therapeutic Area level to support integration of pharmacometrics and relevant (target, compound, disease) knowledge in the planning and execution of robust development programs and strategies, independently but in coordination with the PMX Development Unit leader. • Lead or significantly contribute to initiatives at global line function level, or cross-functional Development Unit level, requiring coordination of diverse of team members. • Lead the review and implementation of Health Authority guidances • Develop and mentor pharmacometricians. • May have 6 PMX scientists direct reports providing support to the disease/therapeutic area. 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: • Ph.D. in pharmacology, biology, engineering, mathematics, statistics, computational science, or a field with significant modeling-related content (or equivalent) with 8+ years relevant work experience; 6+ years in applying, and mentoring model based methods in pre-clinical and clinical drug development. • Track record of identifying and leading contributions to external white-papers/policy that shape best practice in pharmacometrics. Has internally and externally established track record of developing/establishing pharmacometrics excellence. Record in contributing to scientific improvement/change initiatives. • Expert knowledge and evidence of hands-on experience in the application of pharmacometrics methods to drug development • Evidence of consulting skill in the drug development context, i.e. within project teams and management boards; experience interacting with regulatory agencies. • Clinical, pharmacological and therapeutic knowledge in one or more disease areas • Proven expert scientific leadership skills demonstrated in facilitating and optimizing the (pre/early/full-) clinical development strategy. • Fluent in English (oral and written) Highly Desirable: • Excellent communication and presentation skills and in particular the ability to effectively represent pharmacometrics issues to a wide range of target audiences. Location: This position can be based out of East Hanover NJ, Cambridge, MA or Basel, Switzerland You’ll receive: Competitive salary, annual bonus, pension scheme, share scheme, health insurance, 25 days annual leave, flexible working arrangements, subsidized dining facilities, employee recognition scheme and learning and development opportunities as well. 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. Novartis is an equal opportunities employer and welcomes applications from all suitably qualified persons. 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? 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 Global Drug Development Business Unit CD&A 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 335902BR Sep 15, 2022 France Job Description 10 million doses, this is what the Huningue Biotechnology Center produces every year, which is a reference center in the production of bio-drugs, clinical and commercial, by growing mammalian cells. "Quality and safety depend of course on our high-tech equipment, but they also and above all come from our teams, who bring innovation and improvement for the patient," explains Paula Rosa, site manager. Come and join a committed team of 700 people, in a motivating environment. Your responsibilities: As such, your responsibilities include, but are not limited to: • Support the optimization and evolution of biologics bulk drug substance manufacturing processes for commercial and late clinical phase products, through process understanding and applied science. • Drive enhancement of the manufacturing process understanding through, multivariate data analyses, statistical analyses and process modelling. • Identifying areas for improvement in process stability/variability or performance and drive opportunities for process improvement, including innovative technologies • Provide technical leadership for complex issues and optimization and improvement projects of biologics bulk drug substance manufacturing processes • Drive/Coordinate troubleshooting of complex issues of biologics bulk drug substance manufacturing processes • Drive/Coordinate the major changes of the manufacturing processes. • Lead transfer of technical knowledge and processes in close collaboration with the production unit, process development, other sites and global MS&T network to ensure products quality, on-time supply of our products to our patients. Diversity & Inclusion / EEO Novartis s'engage à créer un environnement de travail exceptionnel et inclusif, ainsi qu'une équipe diversifiée, représentative des patients et des communautés que nous servons. Minimum Requirements What you’ll bring to the role: • Strong and agile communication skills, you will act as the advocate for your project(s) and you will represent Huningue’s MS&T department in either local or global project teams or relevant product boards. • Solid experience in data management, statistical analysis of manufacturing processes. • Solid Knowledge in biological drug substance manufacturing • Lead investigation teams, taking into account product environment constraints (e.g., business continuity, planning). Ensure appropriate stakeholder engagement and support, and clearly communicate on progress and issues, presenting technical analytical data clearly and concisely. • Experienced in project and stakeholder management is desirable. • GMP knowledge and understanding is desirable. Desirable requirements: • PhD with 5-7 years, MSc with at least 7 years of professional experience in process development purification or commercial manufacturing purification (large or small scale), preferably in the biopharmaceutical industry • Languages : English (fluent or professional proficiency), French (at least basic level with willingness to learn) You’ll receive: • A competitive salary • An annual bonus • A focus on your career development • Access to our Quality of Life at work programme • Flexible working • Advanced social coverage for you and your loved ones • 27 days of paid leave & 14 days of RTT per year • Various employee recognition programs Why consider Novartis? 799 million. That’s how many lives our products touched in 2019. 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! Novartis has been certified as a "Top Employer" in France 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/network Division Novartis Technical Operations Business Unit NTO LARGE MOLECULES Location France Site Huningue Company / Legal Entity Novartis Pharma France SAS Alternative Location 1 Belgium Alternative Location 2 Germany Alternative Location 3 Switzerland Functional Area Technical Operations Job Type Temps plein Employment Type Permanent Shift Work Non Apply to JobAccess Job Account

Job ID 345801BR May 24, 2022 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. 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 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 reasonable accommodations The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] 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. https://www.novartis.com/careers/careers-research/notice-all-applicants... Why consider Novartis? 799 million. That’s how many lives our products touch. 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! 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 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 352786BR Oct 03, 2022 USA Job Description 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. 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 inhouse 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. Your responsibilities include, but are not limited to: • Lead complex development and commercial stage S&E projects in the solid tumor space • Lead an efficient triage and prioritization in-line with strategy leveraging in depth knowledge in disease area, industry trends and the competitive landscape to deliver prioritized partnering opportunities. • Lead a cross-functional team of internal subject matter experts to make a go/no-go recommendation for potential candidates (strategic fit with Therapeutic Area objectives, portfolio evaluation, and overall attractiveness). • Present to internal senior management and senior leadership while participating on the deal team throughout the process to drive internal decision-making on opportunities. • Partner with Strategy & Growth, Therapeutic Area and BD&L Leadership to develop a partnering strategy in alignment with the enterprise-level strategy and objectives. • Primary point of contact for potential partner companies for assigned Therapeutic Areas and responsible for positioning Novartis as a partner of choice. • Provides a deep understanding of the business, competition and external market; works with Strategy & Growth team and keeps partnering databases accurate. • Collaborates with NIBR S&E to represent the partnering interests of the assigned Therapeutic Areas and to ensure seamless management of external partner relationships across research and development stages. The role can be based in either Switzerland or USA. For US based applicants: This position can be located at the Cambridge, MA and/or East Hanover, NJ sites and will not have the ability to be located remotely. This position will require 25% travel as defined by the business (domestic and/or international). 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 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 What you'll bring to the role: • Higher degree in the medical or life sciences. • 10+ years’ experience in Pharma/Biotech (of which 3+ years in a licensing, alliance management, project management, strategy consulting, strategic planning, portfolio management or commercial strategy role). • 5+ years of demonstrated leadership including management in a matrix environment, across functions, regions and countries. • Track record of 7+ years of interpreting complex information of both a commercial and scientific understanding externally and internally. Desirable: • Some formal business education • Additional language skills #transformingforgrowth Why Novartis? 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. 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 Accessibility and reasonable accommodations: The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] 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. https://www.novartis.com/careers/careers-research/notice-all-applicants...Division NIBR Business Unit BUSINESS DEVELOPMENT & LICENSING - NIBR Location USA Site Cambridge, MA Company / Legal Entity NIBR 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 352792BR Sep 30, 2022 USA Job Description 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. 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 inhouse 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. Your responsibilities include, but are not limited to: • Lead complex development and commercial stage S&E projects in the Hematology space • Lead an efficient triage and prioritization in-line with strategy leveraging in depth knowledge in disease area, industry trends and the competitive landscape to deliver prioritized partnering opportunities. • Lead a cross-functional team of internal subject matter experts to make a go/no-go recommendation for potential candidates (strategic fit with TA objectives, portfolio evaluation, and overall attractiveness). • Present to internal Senior Management (TA alignment) and Senior Leadership (xTED and ECN DC as appropriate) while participating on Deal Team throughout process to drive internal decision making on opportunities. • Partner with S&G and Global Head of S&E to develop disease area partnering strategy in alignment with the strategy of the assigned TA’s and the objectives set on an enterprise level. • Primary point of contact for potential partner companies for assigned Business TA’s and responsible for positioning Novartis as a partner of choice. • Provides a deep understanding of the business, competition and external market; works with S&G team and keeps databases (IRIS, Inova) accurate • Collaborate with other Novartis business development groups, primarily NIBR S&E, to represent the partnering interests of the assigned TA’s and to ensure seamless management of external partner relationships and early stage evaluations where applicable. The role can be based in either Switzerland or USA. For US based candidates: This position can be located at the Cambridge, MA and/or East Hanover, NJ sites and will not have the ability to be located remotely. This position will require 25% travel as defined by the business (domestic and/or international). 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 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 What you'll bring to the role: • Higher degree in the medical or life sciences. • 10+ years’ experience in Pharma/Biotech (of which 3+ years in a licensing, alliance management, project management, strategy consulting, strategic planning, portfolio management or commercial strategy role). • 5+ years of demonstrated leadership including management in a matrix environment, across functions, regions and countries. • Track record of 7+ years of interpreting complex information of both a commercial and scientific understanding externally and internally. Desirable: • Some formal business education • Additional language skills #transformingforgrowth Why Novartis? 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. 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 Accessibility and reasonable accommodations: The Novartis Group of Companies are committed to working with and providing reasonable accommodation to individuals with disabilities. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please send an e-mail to [email protected] 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. https://www.novartis.com/careers/careers-research/notice-all-applicants... Division NIBR Business Unit BUSINESS DEVELOPMENT & LICENSING - NIBR Location USA Site Cambridge, MA Company / Legal Entity NIBRI 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 351770BR Sep 09, 2022 USA 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 new technologies that have the potential to help produce therapeutic breakthroughs for patients. In the Portfolio Anatomical Pathologist role within the Preclinical Safety team you will provide strategic team leadership on pathology aspects of drug discovery and/or development projects and initiatives throughout the lifecycle and/or lead broad technology development areas within department and NIBR. You will successfully operationalize key scientific/technical/development areas to advance department and division goals. You must be recognized as a strong team leader and/or a deep expert in your area; assess impact, limitations, and added value of scientific activities in order to define team's strategic objectives, advance related projects, and/or significantly expand scientific/technical knowledge within one or several related areas of deep expertise and relevance to NIBR. At the Director level in portfolio pathology you will fulfill the above and also demonstrate the ability to implement and/or provide input to enable division-wide strategy for new discoveries, platforms and/or development. To be eligible for a director level role you will also enable impactful experimentation, project initiation, and decision making by leading/empowering an interdisciplinary team or by creating and driving scientific, functional and technical communities surrounding your area of deep expertise and thought leadership. Your major accountabilities will include but not be limited to: -Generate, evaluate, and interpret pathology data and/or conducting pathology peer review for assigned studies, including reporting the results of these investigations as sections of submissions to regulatory agencies. -Monitor and review pathology procedures and data during the performance of studies by outside contractors. -Maintain collaborative and constructive interactions and information flow with other members of the target and drug project teams. -Provide support and interpretation through a variety of techniques including but not limited to histopathology, morphology, computational and digital pathology, electron microscopy and/or carcinogenicity assay design, evaluation and/or peer review. In addition, you will influence the development and practice of toxicologic pathology and drug development through participation on scientific boards, project teams, and advisory committees and may be asked to function as project team representative for preclinical safety. You will be expected to participate in the study design and in the evaluation and implementation of new procedures to improve the operations. A current knowledge of recent advances and new equipment/procedures is important to achieve optimum results. You may be responsible for making recommendations toward the development of an annual budget and may be asked to provide input towards hiring and other evaluations, may be asked to assist the management in training the other pathologists, and may be assigned to projects with more complex design and/or those requiring the most advanced interpretive experience and knowledge. At the conclusion of a study, the candidate is expected to participate in the data review/analyses and determine target organ toxicity. You will also perform other duties as assigned by the management. -Senior Principal Scientist level: Establish and lead novel projects in emerging strategic scientific/technical/development areas. Recognized as a key expert in her/his area, develops ideas with team members and collaborates across multiple different therapeutic areas, modalities and/or initiatives. Provides subject matter leadership and connects a team to enable project progression, and/or identifies key connection points with own area(s) of deep expertise to progress department and Division strategic priorities. Recognizes and leverages external collaboration opportunities. Associate Director level: Above plus provides strategic leadership on drug discovery and/or early development projects and initiatives throughout the lifecycle, and/or lead broad technology development areas within department and division. Director level: Accomplish the above and directly lead diverse team(s), including setting, achieving, and empowering others for developmental objectives and providing depth of expertise in business applicable areas including international involvement as an expert. 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 will bring to the role: Required: Ability to interpret toxicologic pathology results and write reports, regulatory documents and scientific manuscripts. Ability to supervise Preferred: Board certification in related fields (e.g., DABT) Management experience History of scientific publications/presentations in peer-reviewed journals or relevant scientific meetings. Pharmaceutical company experience with drug discovery and drug development from early phase through registration. Ideal Background Education & Qualifications Minimum: DVM/MD degree (or equivalent) with graduate training in pathology and board certification (DACVP/DECVP) in veterinary pathology; post graduate degree (PhD) preferred. Education & Qualifications Minimum: DVM/MD degree (or equivalent) with graduate training in pathology and board certification (DACVP/DECVP) in veterinary pathology; post graduate degree (PhD) preferred. Senior Principal Scientist – 5 plus years toxicologic pathology experience required Associate Director 8 plus years toxicologic pathology experience required; pharmaceutical drug development experience preferred Director – 12 plus years related pharmaceutical drug development experience required; team leadership experience required; and regulatory filing experience strongly preferred. 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.Division NIBR Business Unit Translational Medicine Location USA Site Cambridge, MA 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 351601BR Aug 29, 2022 USA 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 new technologies that have the potential to help produce therapeutic breakthroughs for patients. As a Study Monitor in the Preclinical Safety group within NIBR's Translational Medicine team you will be appointed to each outsourced preclinical study based on relevant technical expertise, designated disease area and/or scientific background knowledge and act as the primary scientific contact for the Study Director at the Contract Research Organization (CRO). In this role your main accountabilities will not be limited to: - Oversee the progress of the study and for ensuring that the study is conducted, recorded and reported according to the study protocol. - Ensure that the study is compliant with the appropriate GLP regulations, Novartis animal welfare policies, CRO in-house standard operating procedures, Novartis expert recommendations (where feasible) and all relevant international regulatory guidelines/regulations. - Resolve study related issues and liaise with internal experts and inform the relevant people in a timely manner is pivotal to the performance of this role. - Strategically overview and track the study phases and sample delivery timelines to ensure that internal contributor reports are delivered to the CRO on time and that the CRO meets its agreed main reporting timelines. Position can be based in East Hanover, NJ; Cambridge, MA or Basel, Switzerland 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: 2 plus years experience in the role of Preclinical Study Director/Study Monitor; experience as a Project Team Member/Representative is a plus. Educational qualifications: Bachelors degree required; Masters or PhD preferred. Solid scientific background in Toxicology gained in either the Pharmaceutical and/or CRO industry. Registration and certification with one of the International Toxicology registers is desirable. 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. Vaccine Policy: While Novartis does not require vaccination at this time, for certain Novartis sites in the US all associates and candidates may be required to either upload an image of their COVID-19 vaccine card demonstrating proof of full vaccination for COVID-19 (or other similar evidence of vaccination) or proof of a negative COVID-19 test taken by the associate or candidate within the past seven days to enter any of our sites and/or customer office or healthcare facility, as well as prior to participating in other work related off-site meetings. Employees working in customer-facing roles must adhere to and comply with customers’ (such as hospitals, physician offices, etc.) credentialing guidelines, which may require vaccination. As required by applicable law, Novartis will consider requests for reasonable accommodation for those unable to be vaccinated. This requirement is subject to applicable state and local laws and may not be applicable to employees working in certain jurisdictions. Please send accommodation requests to [email protected]. 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/networkNo video provider was found to handle the given URL. See the documentation for more information. Division NIBR Business Unit Translational Medicine 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