Novartis AG

Job ID 357249BR Dec 01, 2022 Switzerland Job Description Research Scientist, 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 therapeutic approaches and technologies potential to become breakthroughs therapeutics for patients. You will join an established in vitro immunology lab (1 Lab head, 2 associates) in the department of Autoimmunity, Transplantation & Inflammation (ATI) in Basel. Major accountabilities include: • You will employ a number of sophisticated in vitro technologies such as high-end flow cytometry or other immuno-assays to assess the activation and function of primary cells of blood, vasculature and stroma and of extracellular vesicles • You will take responsibility to design, develop and apply new assays to measure receptor ligand interactions, immune and stroma cell signaling, function or maturation. • Furthermore, you will investigate the pharmacodynamic effects of new drug candidates in animal-samples derived from partnering in-vivo labs. • You will generate hypotheses to test, troubleshoots issues and designs and executes the next set of experiments with some input from senior lab members/manager. • Provide data evaluation, interpretation, documentation of your own work and present to lab and Unit members • Isolates or purifies analyses, and identifies hormones, minerals, proteins, and/or cultures of microorganisms to determine their biological properties. 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: • MS/BS, diploma or have completed an apprenticeship in a life science discipline e.g. immunology, cell biology, or biotechnology with several years of practical experience in the respective fields. • A good knowledge in immuno-analytical methods including cell culture, flow cytometry, molecular biology and Western blot is desired • Microsoft Office software user, Graphpad Prism • 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 international team. • Very Good organization skills and strong eagerness to discover and evolve translational and drug target-relevant knowledge • Independence within a multidisciplinary environment 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 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 355913BR Nov 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. This position will be in the Protein Sciences group, in which we produce and characterize proteins as well as protein complexes, study their structure and function and use biophysical methods to discover new ligands, validate hits, and characterize these binding events. We are seeking an experienced and collaborative NMR spectroscopist with a strong background in protein dynamics and an interest in drug discovery. You are passionate about applying state-of-the-art NMR technologies to characterize the dynamics and conformational states of therapeutically relevant proteins and to translate this information into drug discovery approaches such as fragment-based screening, hit validation and structural characterization of protein-ligand complexes. You are a hands-on scientist and want to apply NMR with all its versatility to support drug discovery projects as part of interdisciplinary teams. You enjoy strategic thinking and develop as well as implement new ideas of how insights into protein dynamics can shape drug discovery approaches. You are an NMR expert with curiosity for drug discovery and a team player who thrives in a multidisciplinary matrix environment. In doing so, you will have opportunities to develop and grow as a scientist and as a drug hunter. Your responsibilities Your responsibilities include, but are not limited to: • Implementation and application of state-of-the-art NMR experiments to characterize the dynamics and conformational landscape of therapeutically relevant proteins, and changes upon ligand binding • Translation of this understanding of dynamics into drug discovery strategies, and acting on them by performing fragment-based screens, hit validation and structural characterization of protein-ligand complexes • Expression, purification and resonance assignments of isotope-labeled proteins for NMR investigations • Represent NMR spectroscopy in project teams, propose best use of NMR in projects • Provide strategic input to further advance NMR at NIBR 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 knowledge in theoretical and practical aspects of protein NMR spectroscopy in its breadth and depth, especially in protein dynamics and characterization of conformational states • PhD in chemistry, physics, biology or related fields, and postdoctoral experience in solution-state biomolecular NMR spectroscopy • Track record of independent research, publications, and presentations at international conferences • Expert knowledge in protein expression and purification as well as resonance assignments. • Team player in an interdisciplinary environment • Fluent in written and spoken English with effective presentation skills and ability to communicate with non-experts • Understanding of biology and disease mechanisms as well as experience in drug discovery research are 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! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision NIBR Business Unit CBT - NIBR Location 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 356777BR Nov 04, 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. We are looking for an experienced Senior Manager (Employment Tax), who will work in multi-disciplinary teams representing employment tax to address compliance topics in respect of both mobile and domestic employees for designated customer groups within Novartis (across Global Mobility, Equity, Rewards, Group Tax, P&O and Payroll services teams). This opportunity is open for both Swiss and UK associates, as both options of work locations are available for this role. Major accountabilities: • Acts as an expert resource working with designated internal customers groups to design, implement, maintain and monitor employment tax compliance policies, processes and governance structures as per defined Employment Tax strategy. • Provides support and troubleshoots questions from country and regional payroll and employment tax teams. • Leads employment tax projects with customer group, including, but not limited to, implementation of new tax laws, compliance remediation activities etc. • Provides support with monitoring employment tax audits globally, with related risks assessments, processes improvements as well as with implementation of related global governance. • Collaborates with Rewards colleagues to implement new benefits and ways of working at a Global and local level. • Responsible for providing support to customer groups for cross-border associates or Novartis executives, including working with external vendors and tax authorities to pro-pose tax positions, ensure compliant employment set-up aligned to corporate legal entity structure, review the individual tax and compliance impact of proposed packages and working arrangements, and manage any manual interventions required to standard processes to ensure these are compliant. • Prepares PowerPoint materials for various purposes (senior stakeholder meetings to support decision making, trainings for non-technical colleagues) and communicates complex topics in simple and clear manner. 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 • 5-7 or more years of international tax experience, with a focus on employment and individual taxes as well as cross-border taxation • Excellent communication skills (written and verbal) • Proactively builds relationships, good team player • Working knowledge of HR, equity and payroll processes and tools and benefit plans • Experience working in complex multi-national corporations, as well as experience with working in virtual teams • Policy design, process improvement and mapping/design • Working knowledge of end-to-end international assignment processes including payroll, tax, social security • Experience of working in corporate tax, finance or audit and/or Swiss tax and social security authorities (Basel Stadt/Basel Land) and US tax are beneficial 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 GROUP PEOPLE & ORGANIZATION Location Switzerland Site Basel Company / Legal Entity Novartis International AG Alternative Location 1 United Kingdom Functional Area Human Resources Job Type Full Time Employment Type Regular 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 355715BR Nov 30, 2022 Switzerland Job Description Novartis Institutes for BioMedical Research (NIBR) is the global pharmaceutical research organization of Novartis. With approximately 6,000 scientists and physicians around the world, our research is focused on discovering innovative new drugs that will change the practice of medicine. Over 3000 NIBR scientists regularly document their experiments in their electronic Laboratory Notebook. For some of them, it is the centre of their scientific workflow. As the Scientific Product Manager with responsibility for the Biology eLN, you will be responsible for NIBR’s Biology eLN and its positioning in the research informatics product and data landscape. You will establish a sustainable and future-looking strategy and execute on its delivery to provide NIBR scientists with the best eLN experience, striking a balance between legal, compliance, and scientific requirements. Your key responsibilities will include but are not limited to: • Lead a matrixed, multi-disciplinary product team composed of engineers, business analysts, service managers, and support specialists to deliver the desired outcomes for your customers. • Collaborate with the eLN Steering Committee and the Subject Matter Expert community to define your product’s roadmap • Work closely with the Chemistry eLN Product Manager to identify potential synergies • Establish and maintain relationships with Software vendors • Collaborate with other Product Managers to define and deliver end-to-end solutions for scientists • Where necessary, ensure that GxP standards and policies are followed. The role can be based in either Switzerland and/or USA. For US based candidates: The ideal location for this role is East Hanover, NJ but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific East Hanover, NJ for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 20% travel. Diversity& Inclusion/EEO: 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 Video https://www.youtube.com/watch?v=ggbnzRY9z8w 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: • Relevant experience in scientific software product management and/or integrating off-the-shelf software products into a complex scientific product landscape • Background in Biology, Chemistry, or related scientific field • Outstanding communication skills • Courage to question the status-quo and propose innovative solutions • Curiosity to keep learning about science • Experience with Agile software development • Team-over-self’ attitude • Acting with integrity according to clear and visible values The pay range for this position in the USA at commencement of employment is expected to be between $160,000 and $250,000; however, while salary ranges are effective from 1/1/22 through 12/31/22, fluctuations in the job market may necessitate adjustments to pay ranges during this period. Further, final pay determinations will depend on various factors, including, but not limited to geographical location, experience level, knowledge, skills and abilities. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision NIBR Business Unit CBT - NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Functional Area Information Technology Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358232BR Nov 21, 2022 Switzerland Job Description 105,000 associates here at Novartis aligned to a single inspirational purpose; to reimagine medicine! Reporting to the CEO, the Corporate Strategy team drive high profile, company-wide strategic initiatives that address the top priorities for the company whilst supporting the five core pillars of our Strategy: Unleash the power of our people; Deliver transformative innovations; Embrace operational excellence; Go big on Data & Digital and Return more to society. While our roles are highly visible and demanding, we have a unique opportunity to shape global healthcare trends and work with senior leaders across our businesses to execute our company’s agenda. Your responsibilities include, but are not limited to: • Independently drives strategic business projects for Novartis Group, the CEO and the Executive Committee • Generates strategic insights based on best-in-class analysis, distills outputs and recommendations which enable informed decisions of top-level leaders • Actively contribute to annual strategic planning process • Invests in knowledge / functional spike on behalf of strategy team • Proactively identifies trends and opportunities to shape the CEO and ECN agenda • Provide insight into Health Care Systems as our core customer • Develop network of functional experts and strategy managers across Novartis 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: • MD, PhD or MBA from a top business school preferred or equivalent on-the-job experience • High proficiency in English • Deep knowledge of the Pharma industry • At least 4-5 years of consulting experience at a top tier consultancy (engagement manager or associate principal level) • Extensive project and program management experience in strategic projects • Track record of strong business impact Why consider Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network: https://talentnetwork.novartis.com/networkDivision CORPORATE Business Unit Group Corporate Affairs & Global Health Location Switzerland Site Basel Company / Legal Entity Novartis International AG Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 339505BR Oct 21, 2022 Switzerland Job Description 10! That’s how many pipeline projects Immunology has in Phase 3 or registration and over 25 projects in Phase 1/2. Our Immunology Unit has a pipeline with depth and breadth and is known to be a talent powerhouse. We are uniquely positioned to have a critical impact on bringing innovative medicines to patients across multiple disease areas. This includes developing Novartis’ multi-blockbuster Cosentyx and several novel agents, with an extensive immuno-dermatologic footprint. As Global Program Head, you will have a critical impact of delivering innovation, which drives the Novartis enterprise. You will lead Novartis program(s) through the end-to-end development cycle to seek successful registration and market access. You will drive optimal life cycle management of approved assets, and have overall accountability for quality, time, cost, proactive risk management, and compliance. Furthermore, you will work closely with The Novartis Institutes for BioMedical Research (NIBR) to develop overall disease area strategies and advise the research and early development efforts. You will drive global development, worldwide regulatory approvals, market access and optimized commercial value of the program and are accountable for timelines and budget Your responsibilities will include: • Lead a multidisciplinary team of functional experts focused on securing global regulatory approval, market access and optimized commercial value of the program while ensuring this is achieved with a high quality, full compliance (internal and external, e.g. regulatory, requirements) within budget and in a competitive and timely manner, utilizing both the internal or other identified expert resources necessary for success • Establish short and long range project vision and strategy • Ensure alignment/close collaboration cross global functions, regions and CPOs in regards to strategy and direction • Leverage knowledge, experience, understanding of external stakeholders, internal team capabilities and portfolio needs to develop a compelling, innovative vision and strategy for the program • Establish program strategy and execute implementation through milestones and decision points by leveraging cross-functional teams • Presentation and alignment of project strategy • Communicates clear strategy to program team and functions and ensures that it is reflected in the operation • Ensures rigorous adherence to quality and compliance • Drive talent acquisition among team members and within their sub-teams including active selection and de-selection and performance management of the core membership of the program team • Actively coach and partners with direct reports to build and implement individual development plans and conduct their performance appraisal discussions in close partnership with the line-function heads 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: • MD or PhD degree in the related discipline • Minimum of 5 years of drug development experience, including experience in Global Program Teams and with dossier submission for new or supplemental indication • Deep drug development experience in immune mediated and/or dermatology diseases. • Prior exposure to and strong awareness of regulatory / market access / commercialization requirements. • Leadership of multidisciplinary teams • Innovative strategic attitude **Some restrictions to flexible working models may apply and will be discussed at 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 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 IHD DU 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 357690BR Nov 18, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. This role is responsible for a consistent, cross-functional brand strategy shaping and implementation, for all assets having moved from Global to International TA until the handover to IBBI. The incumbent will evolve globally created early brand strategies, such as the Integrated Product Strategies (IPS) into a competitive, truly cross-functional launch plan that is fit-for-purpose for core IMI markets and sets a foundation of launch success for Novartis’ next blockbusters. Incumbent will lead strategic, cross-functional decisions for International and above-brand strategic initiatives, incl. partnerships, policy shaping, and for launched assets, will monitor and respond to major events and competitive landscape developments. The role will include a close interaction with core IMI markets, incl. pro-active co-creation, 1:1 support and serving as the escalation point for risks and opportunities to the Head of International TA. The incumbent will closely collaborate with MAP and CE&E teams to shape launch deliverables and TA-relevant customer experiences/ journeys and campaigns/ content for major IMI markets. On the overall brand strategy level incumbent will collaborate with respective IM-US counterpart to ensure consistent brand positioning worldwide, leverage learnings and transferable practices. Your responsibilities include, but not limited to: • Lead International Solid Tumors TA team • Evolve and operationalize globally created early disease area (DA) teams’ objectives, strategies, and ecosystem shaping strategies for major IMI markets • Drive definition/ execution of above-brand ecosystem initiatives (e.g., partnerships) across DAs and brands and collaborate with the CE&E and MAP to incorporate best practice approaches into ecosystem shaping/ engagement • Partner with major IMI markets to adapt and operationalize globally created, early IPS into a competitive, truly cross-functional roadmap for launch assets • Contribute to launch sequencing and track major IMI market launch preparation progress, risks, and opportunities • For priority assets, drive continuous evolution of IPS / brand plan during growth phase until handover IBBI; in particular, monitor and guide strategic response to events and competitive landscape developments • Drive effective, tiered market support to interpret, localize and operationalize launch strategies and deliverables, acting as primary interface and escalation point for major IMI markets • Partner with MAP and CE&E teams to ensure effective collaboration in shaping of TA-relevant launch deliverables and customer experiences/ journeys / campaigns/ content for major IMI markets. Ensure appropriate compliance against company policies and procedures Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role • At least 15 years senior level pharmaceutical commercial, marketing, medical, access, or R&D experience successfully driving growth of multiple brands in oncology space • Experience in creating competitive, actionable launch strategies in major IMI markets, ideally in the General Management / Country President role. • Experience in innovative omnichannel / digital customer engagement and ability to orchestrate digital engagement channels in building new brands (preferred, not required) • A successful track record of successfully working within matrix with Commercial, Medical Affairs, Market Access Desirable: • Experience in working in high-performing teams in an environment of shared outcomes and cross business accountabilities (highly preferred) • Significant experience from one of the following markets: CN, JP, EU5, AUS, CAN. Experience in above country (regional or global) role #transformingforgrowth 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 PHARMA Business Unit GLOBAL PRODUCT & PORTFOLIO STRATEGY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Commercial & General Management Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358179BR Nov 16, 2022 Switzerland Job Description Job Purpose: • To lead the Sandoz Technical Operations Finance group and to develop and implement processes and projects to further improve transparency, efficiency, integrity and productivity in Sandoz Technical Operations leading to lower COGS, Capex, Investments, Inventory and therefore enhancing CFROI and CVA. • Lead and manage all Business Planning & Analysis (BPA) activities globally through fully integrating planning processes, increasing business impact of the BPA organization and providing financial support to Head TechOps. • Through collaboration and ownership, contribute to building and serving as a role model for a high-performing and inclusive leadership team who deliver synergies together and develops a community of diverse talent to create the best TechOps organization in the industry. Key Responsibilities: • Contribute to the Sandoz Manufacturing Strategy (location, currency, internal vs. external etc.) with specific focus on enhancing CFROI / CVA across Novartis (Cost and Capex) • Develop and implement initiatives to further support the improvement of productivity and operational excellence in Sandoz Tech Ops (->TPC, cost and capex) • Lead all financial planning processes for the TechOps organization worldwide (Budget, Rolling Forecasts, Strategic Plan Financials, Latest Estimate, Latest Outlook, updates to the CEO/CFO, spot landings, monthly business reviews and proactive monitoring of Risks and Opportunities), and provide financial support for acquisitions and divestitures. • Set up and continuously improve funds flow processes and tax positions • Improve quality and speed of decision making in Tech Ops based on accurate and relevant financial data • Lead proactive Tech Ops Finance organisation with strong business partnering capabilities enhancing support to operations & function Heads • Assure highest quality accounting and reporting compliance • Role-model leadership and foster a high performing team culture. Ensure a talent strategy is developed and implemented to support the business strategy, with relevant measures to track performance • Strong focus on transformation as a result of new strategy, MSA activities, M&A • Working closely with commercial in relation to COGS • Develop functional capabilities in Tech Ops Finance supported by the appropriate training, project assignments, job rotations, mentoring Key Performance Indicators: • Financial and Business Results: o COGS (as % of Sales) o Cash (Inventory Levels and Capex Spend) o Customer satisfaction with decision support, early warnings, special projects/tasks • Operational Excellence: o Compliance - Internal & External Audit success rate o Internal customer satisfaction o Innovation and effectiveness of systems, tools and processes • People, Capabilities, and Management: o Tech Ops Finance employee satisfaction and retention o Associate hiring & development: succession planning, development, talent export Job Dimensions: Subordinate Functions: Direct: 6, Indirect: 25 Number of Associates: Direct: tbc, Indirect: tbc Financial responsibility (where appropriate): COGS (USD 5bn), Inventory (USD 2bn) and CAPEX (USD 300mn) Impact on the organisation (where appropriate): Transparency and outstanding decision support driving enhanced CFROI and CVA across Sandoz. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Education: University degree in economics, finance or equivalent – ideally MBA. Languages: English & local country language Experience & Skills: • Extensive experience (12-15 years) in financial roles (analysis, planning and accounting), with record of increasing responsibility • Excellent people and business leadership skills, with proven ability to influence peers and develop other financial professionals • Process optimisation qualification and experience highly desirable to effect clear LEAN methodology and execution • Strong, proactive business results-focus, with proven ability to provide insights that drive business performance • Finance leadership experience in Manufacturing context • Excellent project management & business case building capabilities • Solid understanding of relevant funds flow, tax and governance codes, with ability to ensure compliance across organization • Solid understanding of Sandoz business cycle, financial challenges and regulatory environment • Excellent oral/written communication skills and presentation abilitiesDivision Novartis Technical Operations Business Unit NTO SANDOZ TECHOPS Location Switzerland Site Basel Company / Legal Entity Sandoz AG Alternative Location 1 Germany Functional Area Audit & Finance Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358178BR Nov 16, 2022 Switzerland Job Description • The Head Technical Accounting ensures effective oversight and monitoring of adherence to accounting policies, procedures and financial controls are in place to provide the organizational units with high quality, compliant accounting standards advice and documentation, respecting the Novartis Accounting Manual (NAM), IFRS, Swiss, US and other regulatory requirements and Novartis Financial Controls Manual (NFCM). • The position is the functional leader of the technical accounting team across FRA and for the entire Group, and is responsible to assist the Chief Accounting Officer in the interpretation and implementation of IFRS accounting standards and IFRS and regulatory (i.e. SEC/SIX) reporting requirements. • Position supports Finance Management to produce high quality external financial statements and management financial reports that comply with NAM/IFRS accounting and disclosure requirements, as well as with the requirements of Management for internal Management reports. Key Responsibilities: • Provides technical accounting and reporting guidance and oversight, and monitors accounting for complex transactions, such as M&A, distribution agreements (revenue recognition), Business Development and Licensing transactions, innovative pricing models, factoring in collaboration with the Heads FRA IMI and IM US, and with the CFOs of the Divisions/Units. • Provides thought leadership in assessing implications of proposed / upcoming changes in accounting and reporting standards, including where appropriate soliciting insights from industry peers, participation in SwissHoldings committees on accounting and reporting matters, and the external auditors. • Leads in the interpretation and application to the Company of new accounting and reporting standards, including ensuring their timely and compliant implementations. • Manages requests and recommends revisions relevant to NAM, ensuring the NAM remains up-to-date and aligned to /consistent with IFRS and regulatory reporting requirements (i.e. SEC and SIX) and Novartis accounting principles and guidelines. • Maintain library of accounting position papers for important transactions, ensuring consistent accounting assessments across same or similar types of transactions. • Quality assurance over external financial reporting, ensuring compliance with IFRS and regulatory requirements (e.g. SIX and SEC), and as required in collaboration with Novartis corporate lawyers, IR, and external auditors. • Leads team of technical accounting experts and sets clear objectives and serves as a back-up for direct reports. • Functional lead of the technical accounting specialist teams and ensures, together with the team, high quality, compliant, timely and efficient technical accounting support of the business. • Designs presentations and trains associates on organizational units and regional level on financial reporting and technical accounting. • Role model for leadership style which is inclusive, proactive, respectful, change agile, innovation/creativity and results driven, always with focus on high quality and high integrity and fosters a speak-up culture. Key Performance Indicators: • Quality of accounting and reporting instructions, accounting position papers and support given to the FRA and the technical accounting teams • Responsive / timely interactions with unit management on accounting standards and accounting implications of transactions, new agreements/contracts, etc. • Ensures high quality, timely and efficient technical accounting support of the business. • Effective communication with Chief Accounting Officer on accounting issues and analysis of impact of new accounting and reporting requirements • Development of Finance talent, ensuring training programs up-to-date and delivered, key talent retention and succession planning in place, associate engagement • Quality of presentations to Management on accounting standards and accounting implications of important transactions • Passion for understanding and communicating new accounting requirements • Successful project work to develop new reporting requirements Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Education: • University Degree in finance, accounting, economics and/or MBA; • Certified Public Accountant/Chartered Accountant with in-depth IFRS knowledge Languages: • Excellent English both spoken and written. • German or other European language will be a plus Experience & Skills: • Relevant work experience in finance of 10+ years, with a multinational and/or Audit experience with a major (i.e. Big 4) public accounting firm. • Strong technical accounting competence acquired in Auditing: minimum 8 years in major auditing company, of which 5 years in a multinational financial reporting environment or senior technical specialist in major international company using IFRS or US GAAP • Line management experience with team responsibility • Good SAP ERP understanding a plus • Six Sigma Green belt certification beneficial • Good understanding of the Healthcare industry • Excellent technical knowledge on International Financial Reporting Standards (TL) • Good knowledge of business environment and value drivers (A) • Experience in working with financial reporting systems and with reporting procedures (A) • Good communication skills (TL) • Good presentation skills including succinct reports to senior management (TL)Division SANDOZ Business Unit Global Finance SZ Location Switzerland Site Basel Company / Legal Entity Sandoz AG Functional Area Audit & Finance Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 352197BR Nov 30, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. In this role you will be accountable for contributing to developing overall, cross-functional programs of a priority disease area/ asset, especially early in lifecycle – focused on shaping assets with strong commercial potential in line with TA priorities. The role provides direction and functional expertise in a cross-functional disease area/ asset team and prioritizes US first with enhanced focus on major markets (e.g., China, Japan, Germany) and ensure close collaboration with Strategy and Early Product, NIBR, GDD and MAP teams. Major responsibilities: • DA / Asset strategy aligned with Therapeutic Area (TA) strategy: Collaborating to ensure definition and execution of a competitive strategy to establish Novartis as true industry leader within the DA/ asset and maximize patient impact by influencing/ partnering across the disease ecosystem. • Asset shaping : Shaping market-relevant assets to become Standard of Care with a focus on US • Collaborate to develop transformative, US-centric Target Product Profiles (TPPs) that are tangible, provide a clear guidance to the GDD organization on what level of evidence is required. • Make data-driven, decisive tradeoffs between needs of US and major markets (e.g., CN, JP, DE) • Integrated early brand strategies: Collaborate to ensure impactful, actionable early brand strategies until handover to International by co-developing Integrated Insights Plan, consolidating and aligning inputs and requirements across functions to achieve deep DA ecosystem understanding (patient journey, competitive, access landscape, HCS budget impact and cost effectiveness analysis) • Brand management across the lifecycle: Accountable for maintaining the integrity, consistency, and evolution of each brand across the lifecycle • Work in a diverse, high performance, cross-functionally matrixed team including identifying and integrating expertise and inputs required from other teams to ensure successful delivery (e.g., MAP) The role can be based in either Switzerland and/or USA. Our selection process will prioritize associates whose roles may be changing or may be impacted as a result of the Transforming for Growth reorganization. For US based candidates: The ideal location for this role is East Hanover, NJ but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific East Hanover, NJ for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 20% travel. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you'll bring to the role: • At least 10 years senior level pharmaceutical commercial, marketing, medical, access or R&D experience successfully driving growth of multiple brands • Deep disease area and asset knowledge (or track record to acquire required DA / asset expertise effectively and rapidly) Preferred: • Experience of strategy development and asset shaping early in lifecycle (from any functional perspective – marketing, new products, access, medical, clinical, R&D) • Prior experience in launching specialty brand(s) in major market(s) (US, CN, JP, EU5, AUS, CAN) • Significant (3+ years) and recent (post 2015) experience in above country (regional or global) role • Significant (3+ years) and recent (post 2015) local US experience preferred; Local US experience includes working in the US market with the local US customers, US health care systems/ systems of care, US payors/ accounts, etc.), driving US market strategy • Established relationships with relevant Global KOLs • Proven experience credibly interacting and influencing stakeholders in research and drug development • Track record of successfully working within matrix of Commercial, Medical Affairs, and Market Access, as well as breaking down functional silos and managing complex trade-offs #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision PHARMA Business Unit GLOBAL PRODUCT & PORTFOLIO STRATEGY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Functional Area Commercial & General Management 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 357657BR Nov 30, 2022 Switzerland Job Description 6 production sites! That's the number of internal cell bank customers we have at Novartis. When you join the CBC Operators team, you have a direct impact on cell bank supply at Novartis. The Cell Bank Center of Basel BDSS is a Manufacturing Unit (MU) responsible for GMP and analytical cell bank manufacturing for Novartis Biologics. The Operator is responsible for the GMP compliant manufacturing process of mammalian cell banks at the Basel Cell Bank Center. Major responsibilities: • Conduct all necessary processing steps of cell banking with highest skill level of aseptic/low bioburden technique (thawing, cell passage, cell counting and cell bank freezing) • Gown aseptically and work in Zone C and under the laminar flow hood for extended periods of time. • Plan, prepare (e.g., stock availability, equipment readiness, cleaning) and execute operations independently (taking initiatives). • Maintain and prepares equipment/environment for use • Work with automated cell processing equipment such as the vial filler. • Perform in process operations such as static sampling and in process environmental monitoring • Documents all steps in the assigned Batch record in line with GMP requirements • Assist on deviation investigations and inspections • Perform other duties as assigned, ie. batch record review, process streamline improvements, safety walk-through • Work with liquid nitrogen for cell bank transport and storage 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 Language: • German: fluent • English: basic Experiences: • Cell culture/cultivation • Cell Banking Technical / Functional Skills & Knowledge: • Strong collaboration skills and team spirit • Manufacturing Process Execution • General HSE Knowledge • Knowledge of GMP • Basic Knowledge of IT Applications & tools You’ll receive: We offer you a challenging, international and interdisciplinary work environment. Investment in people is a priority for Novartis. We offer a range of possibilities for personal development and career opportunities within the group to motivated, qualified people. We offer you a competitive salary and benefit package. Novartis also supports a flexible work-life integration (working remotely, flexi-time schedules, ...). Why consider Novartis? 769 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!Division Novartis Technical Operations Business Unit CONTRACT MANUFACTURING Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358130BR Nov 16, 2022 Switzerland Job Description The NIBR Biologics Center (NBC) is seeking for a motivated postgraduate candidate to explore possibilities on the latest technology of PCR quantification. Digital PCR (dPCR) is a new high-level technology for Copy Number Variation, Absolute Quantification, Rare target detection based on PCR partitioning. Start date: January 2023 or upon agreement Duration: 8 months Your responsibilities: • Explore all activities around digital PCR, the possibilities of this method, and to compare dPCR vs ddPCR (droplet digital PCR) • Establish strong and reliable standard protocols • Find specific references for each cell expression systems or particles (as AAV) • If time permits, to explore the dPCR technology at protein level (PICO, Protein Interaction Coupling Assay) Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Recent master’s degree in Biology (graduation not longer than 6 months ago) • Fluent in English, good communication skills • Enthusiasm for molecular biology, experience with PCR, quantitative PCR or digital PCR • Good organizational and planning skills • Problem-solving oriented and working skillfully • Soft skills: self-driven, motivated, willing to learn, strong team spirit 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!Division NIBR Business Unit BIOLOGICS NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 355903BR Nov 15, 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. With Novartis expanding its horizons in the field of targeted radioligand therapy (RLT), the Oncology department at NIBR is looking for a PhD level Principal Scientist with a strong background in cancer cell biology. Expertise in the field of radiobiology and/or DNA Damage Repair would be desirable. The candidate will join the Oncology Translational Research group located in Basel, Switzerland, and will be responsible to lead a laboratory and projects aimed at supporting the clinical development of cancer therapeutics including radioligand therapies, as well as increasing the mechanistic understanding of targeted radioisotope-based therapies. This is an excellent opportunity to join a world class research team at NIBR in Basel, Switzerland. Through a broad and deep knowledge of cancer biology and in collaboration with peers within the team, the candidate is expected to develop ideas and conduct experiments to understand and validate the effect of radiation caused by radioligand conjugates on various cellular functions including DNA damage repair (DDR) and cell fate, discover combination therapy opportunities, identify molecular predictors of response to cancer therapies and to investigate resistance or survival mechanisms in presence of such drugs. Amongst others, your role will be to define and implement cutting-edge experimental strategies, to produce high quality data to validate concepts, and to translate scientific insights into clinical development strategies in collaboration with the respective project teams. To achieve this, state-of-the-art, hands-on molecular and cell biology experience, as well as proficiency in leveraging and utilizing bioinformatics infrastructure and tools will be required to perform in the role. Strong collaborative team spirit, excellent communication skills and willingness to pro-actively interact across the global organization will be essential to succeed in the role. Excellent mentoring and coaching skills will be a necessary asset to develop lab members scientifically and professionally. Your responsibilities will include: • Define and execute best experimental strategy to deliver interpretable data to test hypotheses, address scientific questions and progress projects • Perform lab work (in vitro) to deliver the highest quality of experimental science • Guide, supervise and develop scientific research associates, as well as manage lab resources in a flexible manner to adapt to changing priorities • Contribute to drug discovery and clinical development projects within multidisciplinary teams • Develop novel ideas and concepts aimed at identifying optimal ways to use cancer drugs, including RLTs/radioligand therapies in patients • Present concepts and projects in a clear, scientifically sound / data-driven and objective manner in different settings and venues • Closely work with multiple teams across expertise groups within Oncology and across 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: • Ph.D. with a minimum of 2-4 years postdoc experience • Strong cancer biology background and track record of scientific accomplishment at high standards • Background in DNA damage repair / radiobiology is highly desirable • State-of-the-art experimental expertise in molecular and cellular biology and proficiency in data analysis (bioinformatics skills considered advantageous) • Excellent communication and presentation skills in English Why consider Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we are 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 is possible, when we collaborate with courage to tackle the world’s toughest medical challenges aggressively and ambitiously. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! *Restrictions on flexible working may apply and will be discussed at interview stages as requiredDivision 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 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 352178BR Nov 29, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. In this role you will be accountable for contributing to developing overall, cross-functional programs of a priority disease area/ asset, especially early in lifecycle – focused on shaping assets with strong commercial potential in line with TA priorities. The role provides direction and functional expertise in a cross-functional disease area/ asset team and prioritizes US first with enhanced focus on major markets (e.g., China, Japan, Germany) and ensure close collaboration with Strategy and Early Product, NIBR, GDD and MAP teams. Major responsibilities: • DA / Asset strategy aligned with Therapeutic Area (TA) strategy: Collaborating to ensure definition and execution of a competitive strategy to establish Novartis as true industry leader within the DA/ asset and maximize patient impact by influencing/ partnering across the disease ecosystem. • Asset shaping : Shaping market-relevant assets to become Standard of Care with a focus on US • Collaborate to develop transformative, US-centric Target Product Profiles (TPPs) that are tangible, provide a clear guidance to the GDD organization on what level of evidence is required. • Make data-driven, decisive tradeoffs between needs of US and major markets (e.g., CN, JP, DE) • Integrated early brand strategies: Collaborate to ensure impactful, actionable early brand strategies until handover to International by co-developing Integrated Insights Plan, consolidating and aligning inputs and requirements across functions to achieve deep DA ecosystem understanding (patient journey, competitive, access landscape, HCS budget impact and cost effectiveness analysis) • Brand management across the lifecycle: Accountable for maintaining the integrity, consistency, and evolution of each brand across the lifecycle • Work in a diverse, high performance, cross-functionally matrixed team including identifying and integrating expertise and inputs required from other teams to ensure successful delivery (e.g., MAP) The role can be based in either Switzerland and/or USA. Our selection process will prioritize associates whose roles may be changing or may be impacted as a result of the Transforming for Growth reorganization. For US based candidates: The ideal location for this role is East Hanover, NJ but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific East Hanover, NJ for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require 20% travel. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you'll bring to the role: • At least 10 years senior level pharmaceutical commercial, marketing, medical, access or R&D experience successfully driving growth of multiple brands • Deep disease area and asset knowledge (or track record to acquire required DA / asset expertise effectively and rapidly) Preferred: • Experience of strategy development and asset shaping early in lifecycle (from any functional perspective – marketing, new products, access, medical, clinical, R&D) • Prior experience in launching specialty brand(s) in major market(s) (US, CN, JP, EU5, AUS, CAN) • Significant (3+ years) and recent (post 2015) experience in above country (regional or global) role • Significant (3+ years) and recent (post 2015) local US experience preferred; Local US experience includes working in the US market with the local US customers, US health care systems/ systems of care, US payors/ accounts, etc.), driving US market strategy • Established relationships with relevant Global KOLs • Proven experience credibly interacting and influencing stakeholders in research and drug development • Track record of successfully working within matrix of Commercial, Medical Affairs, and Market Access, as well as breaking down functional silos and managing complex trade-offs #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision PHARMA Business Unit GLOBAL PRODUCT & PORTFOLIO STRATEGY Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Functional Area Commercial & General Management Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 348934BR Nov 11, 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 Nov 11, 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 355713BR Nov 14, 2022 Switzerland Job Description 250! The number of genomics research projects that are waiting for your data analysis expertise every year. Your work will be important towards faster discovery and development of next generation breakthrough therapies for unmet medical need. The Autoimmunity, Transplantation and Inflammation (ATI) Disease Area at the Novartis Institutes for BioMedical Research (NIBR) and the Immunology franchise in Global Medical Affairs (GMA) are looking for a curious and motivated Associate Bioinformatics Data Scientist to work on the analysis, integration, and interpretation of multiple types of omics data collected as part of our clinical trials in dermatology. The ATI Bioinformatics team provides translational bioinformatics expertise and support to clinical and preclinical drug discovery programs targeting autoimmune diseases and chronic inflammation. We apply systems and computational biology approaches to internal and external biomedical data to enable strategies for disease understanding, target identification, biomarker discovery, indication selection, and patient stratification. Please note this is a 6-month, fixed-term contract position. Your responsibilities: • Application of modern biostatistics and machine learning methods to high-throughput molecular and clinical data. • Analysis, integration and visualization of transcriptomics and epigenomics data, including RNA-seq and DNA methylation. • Contextualization of results from omics experiments, including correlation with clinical endpoints and phenotypes, generation and comparison of molecular signatures, pathway- and network- level analyses. • Communicating with and presenting your work to a diverse audience of biologists, clinicians and data scientists. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Master’s degree (MSc) in bioinformatics, computational biology or a related field, preferably with previous work experience in industry. • Excellent skills in data analysis, data visualization and statistical programming in R/Bioconductor. • Previous hands-on experience with DNA methylation and/or other epigenomics data analysis. • Good knowledge of computational, statistical and machine learning methods for handling high dimensional omics data; Previous experience with in silico deconvolution and/or latent factor models is considered as plus. • Good understanding of biology and basic immunology concepts. • Ability to work independently and as part of an interdisciplinary team. • Excellent communication skills and knowledge of English (oral and written). Why consider Novartis? 750 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 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 AUTO/TRANS/INFL - 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 353092BR Oct 14, 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 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 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. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you will bring to the role: • A PhD and/or MD degree with postdoctoral experience and a minimum of three years of research in renal biology and physiology, preferably in the pharmaceutical / biotechnology industry or academia. • In-depth knowledge of (patho-)physiology of PKD, including direct experience with PKD mechanisms and complex in vitro renal cell-based platforms recapitulating human cystic phenotype and in vivo models of disease progression. • Extensive “hands-on” experience and proven track-record in the use of a wide range of cellular, biochemical and genome editing methods and technologies to unravel complex cellular signaling pathways • Familiarity with “state of the art” computational and analytical approaches and be comfortable with analyzing large scale datasets • A track record of leading drug discovery projects and working alongside disease areas specialists to bring mechanistic target biology and target validation understanding for renal diseases. • Strong communication skills with an ability to effectively interact with people in a dynamic matrix environment, both internally and externally • A proven scientific impact on innovation through a solid publication track record and strong external scientific network with academic experts. • Excellent oral and written communication skills (in English) are essential Why consider Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we are 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 is 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.Division NIBR Business Unit DAX - 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 354493BR Oct 28, 2022 Switzerland Job Description 1996! In this year Sandoz initiated the world’s first biosimilar development program. Over 20 years of experience in biosimilar development have equipped us with extensive knowledge and outstanding expertise in the development, manufacturing and commercialization of biosimilar medicines to the healthcare community and patients worldwide. Global Drug Regulatory Affairs leader supporting Global Program Team(s) (GPTs). Functions independently with minimal supervision as a core member of the GPT to define and implement the global regulatory strategy for the development, submission, approval and life cycle management of the project(s). Responsible for leading a high functioning global regulatory subteam(s) for the program. May also have full regulatory responsibility for one or more early projects with little or no DRA sub-team support as appropriate. Major Accountabilities: • Provide regulatory leadership to assigned project(s). • Develop high quality and globally aligned regulatory strategies to achieve optimal development objectives and life cycle management plans. • Develop global regulatory strategy and plans for Health Authority (HA) interactions as appropriate. • Contribute to and review HA responses, as required, to ensure appropriate, consistent and complete answers to any HA questions. Ensure responses are in line with development strategy. • Lead the global submission planning process, including potential Advisory Committees. • Lead regulatory submission process throughout project lifecycle on behalf of GPT. This includes oversight of submission plan, generation and sign-off of key regulatory/response • Effective matrix management of regulatory team(s) consisting of GPRM’s and other DRA line functions, providing, to the extent possible, mentorship and opportunities for growth and development. 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 6-8 years of regulatory and drug/biologic development experience, ideally spanning activities in Phases I-IV • Prior history with post-marketing/brand optimization strategies and commercial awareness • Major involvement in a CTD/MAA/NDA submission and approval. • Proven success in global drug regulatory submissions. • Proven ability to analyze and interpret efficacy and safety data. • Minimum 2-5 years of demonstrated leadership and accomplishment in all aspects of regulatory affairs in a global/matrix environment in the pharmaceutical industry. • Global matrix management people management experience desirable. • Good management, interpersonal, communication, negotiation and problem solving skills. • Fluency in English as a business language. Additional language is an asset. • Science based BS or MS with requisite experience and demonstrated capability. Advanced degree (MD, Ph D, PharmD) preferred. Why Sandoz? 500 million patients were touched by Sandoz generic and biosimilar medicines in 2020 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 BioPharma SZ Location Switzerland Site Basel Company / Legal Entity Sandoz AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 354528BR Oct 28, 2022 Switzerland Job Description 1996! In this year Sandoz initiated the world’s first biosimilar development program. Over 20 years of experience in biosimilar development have equipped us with extensive knowledge and outstanding expertise in the development, manufacturing and commercialization of biosimilar medicines to the healthcare community and patients worldwide. The Global Senior Manager Regulatory Affairs Sandoz Biopharmaceuticals supports one or more biosimilar/biotech projects, and compiles and prepares high quality regulatory documentation for complex global regulatory submissions worldwide in a timely manner. The Sr Mgr RA is responsible for executing and implementing the regulatory strategy besides providing regulatory and strategic support of assigned biosimilar/biotech project(s) and tasks through development, registration and approval/post approval. The Snr RA Mgr works independently under limited supervision to provide strategic and operational regulatory direction and may support the Regulatory Affairs global program team (GPT) representative and/or GTAL for programs. In certain cases, the Snr RA Mgr may be the GPT Major Accountabilities: • Responsible for implementing regulatory strategy and managing operational activities for assigned regions. • Provides input into global regulatory strategy and contributes to Regulatory Strategy Plans and Seed Document, or their equivalents, including identification of gaps or risks in global strategic plan for assigned regions. • Partners with regions to align on regulatory strategy in order to fulfil business objectives. • Implements strategy across assigned regions. • Works with Regulatory Affairs Sandoz Biopharmaceuticals (RASB) GPT representative and/or GTAL to plan and facilitate presentations to Novartis regulatory boards on regulatory strategy. • Works with RASB GPT representative and/or GTAL to interact with regulatory consultants/advisors for global strategic input and challenge. • Develops and implements regulatory readiness with other line functions, Country Organizations and key opinion leaders, and ensures integration with global regulatory readiness with RASB GPT representative and/or GTAL. • Represents RASB on or leads sub-teams 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 • Mininum 5 years work experience in biotech Regulatory Affairs (proven high learning curve within organization or industry experience gained in relevant fields could potentially being considered) • Excellent data processing skills (incl. MS Office) • Strong knowledge of development processes and of basic science • Strong ability to interpret scientific and commercial information • Strong analytical problem solving skills • Strong strategic and conceptual thinking • Strong ability to construct persuasive scientific/regulatory documents • Good understanding of regulatory requirements for filings worldwide and critical evaluation of emerging requirements, guidelines for new drugs and product life cycle maintenance • Strong ability to work in a complex and international setting • An advanced degree in life sciences/healthcare (PharmD/PhD) or relevant industry experience • Fluent English required (oral and written) Why Sandoz? 500 million patients were touched by Sandoz generic and biosimilar medicines in 2020 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 BioPharma SZ Location Switzerland Site Basel Company / Legal Entity Sandoz AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 357616BR Nov 25, 2022 Switzerland Job Description 100,000. That’s how many patients participate in our clinical trials at any given time. Global Clinical Operations touches patients’ lives every day acting as a link between science and medicine. Envision the impact you could have as the Head of Vendor Program Leads! #GCO In this role you will ensure the development of a program level vendor strategy for the execution and delivery of all global clinical trials across all programs, in accordance with established category strategies. You'll be accountable for the successful execution of strategies to support portfolio deliverables and have complete oversight of budget and resource allocation including enterprise review of VPL resources. You'll provide mentorship to your Program Leads and drive operational excellence through process improvement and knowledge sharing across the function. We want you to develop an empowered organization which can navigate in a matrix environment and adjust quickly to business needs. Responsibilities include but are not limited to: • Lead an organization of 10+ Vendor Program Leads across global locations • Drive efficient allocation and resourcing to Global Clinical Operations (GCO) and Vendor Partnerships & Governance (VPG) priorities. • Establish objectives for VPL organization in alignment with GCO and VPG organization priorities. • Build the best talent and an empowered culture to foster high performance in a matrix environment. • Sponsor key talents across the organization to ensure business critical roles and talent continuity. • Hiring, onboarding, development, and retention of VPLs and serve as the single point of contact for internal/external customers. • Utilize data and insights to monitor overall performance of VPL and be responsible for providing quarterly business review updates on status program strategies, risks and issues from a portfolio view. • Sponsor key initiatives to improve operational efficiency within the Vendor Program Lead organization as well as the broader VPG organization Accessibility and accommodation: Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • We are looking for an industry leader with significant experience and expertise in drug development processes, knowledge of strategic partnership management, and related vendor oversight processes and activities. This will include but is not limited to Regulatory, Trial Management, and relevant development units. • Education (minimum/desirable): Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred (PhD/MD/ PharmD/ Masters) • 10 or more years of experience in pharmaceutical clinical drug development. • Experience in managing associates globally and in management in a matrix organization. • Proven ability to lead cross functional matrix teams • Strong leadership, interpersonal and problem-solving skills. High resilience and ability to advocate and implement new ways of working. • Extensive knowledge of Vendor landscape and vendor service offering how this translates to the clinical development process. • Strong organizational understanding and customer management skills. • Strong relationship-building skills; can influence, negotiate with and motivate executive leadership Why consider Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit GDO GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358868BR Nov 25, 2022 Switzerland Job Description 60% of the world’s population live in Asia, Middle East and Southern Africa region, hosting exciting, dynamic economic and policy environments. Working in the region brings opportunities to partner broadly to expand access to patients and to engage as policies are being shaped. Your talent is needed to help guide us in our policy engagements throughout this region, and support with particular focus on Australia, Korea, Taiwan, Turkey and Japan. You will have a focus on the advanced markets in APMA ( Japan, Australia, Turkey, Taiwan, Korea), supporting in-market PA activities and representing Novartis in above-market activities. You will also lead a policy hub approach to co-develop and implement a Novartis policy agenda in a broader set of advanced markets in the APMA & LaCan region, to shape an optimal business environment that supports our therapeutic areas, fosters innovation, is open to value based approaches and broadens patient access. Key Responsibilities: • Identify key policy priorities for the APMA region in alignment GPA Policy and other functions, develop/adapt relevant policy positions and data to suit the APMA & LaCan region and roll out to countries. • Directly support in-market PA activities for Japan, Australia, Taiwan, Korea and Turkey, which includes managing PA strategy setting and execution, representing these markets with above market external stakeholders and within regional trade associations, and coach and support talent in these markets. • Prepare briefing material, advice and internal reports on these markets for internal and external use. • In close cooperation with Cluster and Global PA representatives, build and lead a policy hub approach, where a broader set of advanced markets in the APMA and LaCan region can share best practices, co-create solutions to shared objectives on short, middle and longer-term policy shaping and partnerships engagements. • Design and implement regional/above – market external platforms for the group of Advanced markets to enhance and expand policy discussions 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 Criteria: • University Degree in relevant area required ( Health/Public Policy, Legal, Pharmaceutical) • Knowledge of advanced health care systems, with focus on pricing and reimbursement and regulatory environments • Extensive experience in Pharmaceutical Market access/Public Affairs/policy • Fluent in English Desirable Criteria • Experience in a pharmaceutical policy/public affairs or business role with some of the following countries: Japan, Australia, Taiwan, Korea, Turkey, Asia Middle East, Africa, Canada and Latin America Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network[SS(1]Division CORPORATE Business Unit GLOBAL PUBLIC AFFAIRS Location Switzerland Site Basel Company / Legal Entity Novartis International AG Functional Area Communications & Public Affairs Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 351615BR Oct 28, 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 354542BR Dec 02, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. We are looking for a Manager Internal Audit who will be a trusted partner for the business to improve governance, risk management, processes and our culture. You will get to engage with senior leaders of Novartis corporate functions and country organizations. You will also be able to further develop your skills and strengths that will help you to reach new heights in the profession in an inspired, curious and un-bossed organization. Your responsibilities include, but not limited to: • Plan, deliver and follow up from assurance and advisory projects in the markets and at the corporate level either as a team lead or team member. • Act as a cultural change agent, supporting assurance function with business partnering. • Manage knowledge and drive innovation to ensure high-quality, value-adding and digitally enabled audit execution. • Contribute to the digital transformation of the audit function to leverage the opportunities presented by current and new technologies and data across the organizations. • Bring a different perspective to review audit methodology projects and continuous im-provement initiatives. • Build and maintain key relationships with stakeholders, establishing a culture of engagement while adding value. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • Bachelor's degree in business related field. Certification of IIA or working knowledge of GAAP and the IIA Standards for the Professional Practice of Internal Auditing is preferred. • 4 to 6 years relevant working experience in internal audit/advisory departments in a big four, in an IA boutique or consulting firm with focus on Pharma or the healthcare sector, OR a minimum of 6 years of experience in the business (e.g. commercial, general management, Finance) with a strong interest in internal audit • Good knowledge of SAP FI and CO modules, ACL, Tableau, Excel or other audit tool • Strong business acumen and knowledge of process management and/or business process optimization • Team-player with project management skills to collaborate effectively across a matrix and Ability to prioritize assignments, deal with interruptions, and meet deadlines in a fast paced and growth-oriented environment • Excellent communication and interpersonal skills including the ability to interact effectively with a wide variety of departments and leaders at all levels of the organization. • Strong analytical skills and ability to process and analyse large data size to identify trends and exceptions together with a positive attitude, pro-active and resourceful. • Proficient in English plus at least one other language desirable, like Russian, French, German, Spanish, or any Eastern European. Willingness to travel up to 30%Division CORPORATE Business Unit BUSINESS ASSURANCE AND ADVISORY Location Switzerland Site Basel Company / Legal Entity Novartis International AG Functional Area Audit & Finance Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 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 357178BR Nov 24, 2022 Switzerland Job Description Get experience in a dynamic tax environment of a multinational pharmaceutical company, which offers exciting tax transfer pricing projects, team diversity and working flexibility. Timing: expected start date: February or March 2023 Duration: 3 months (option to extend) Your responsibilities: • Assist in preparing the Novartis Master File and Local File in accordance with OECD BEPS requirements, in coordination with internal and external stakeholders • Prepare market industry reports and organizational charts for the annual TP documentation process • Support TP compliance of the Group entities through TP policy & guidelines, intercompany agreements, etc. • Support in performing tax research activities and financial analysis for TP matters. • Collect external developments on local TP legislations and / or regulations from external consultants (e.g. through newsletters, yearly TP country books, etc.) 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: • Current Bachelor or Master student in economics, business administration or law • Fluency in English, both written and spoken is mandatory. German or any other Swiss language is a plus • First work experience is a plus, but not mandatory • Open to work in a cross-functional international environment 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!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 355905BR Nov 10, 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 Oncology Research department at Novartis Institutes for Biomedical Research is recruiting for a Ph.D. level Senior Principal Scientist/Associate Director with a strong background and track record in cancer cell biology. Expertise in the field of radioligand therapy development and/or radiobiology would be desirable. The candidate will join an Oncology Drug Discovery Research group located in Basel/Switzerland and will be responsible to lead projects in the areas of oncology drug discovery and radioisotope-based therapies. In addition, the successful candidate will work closely with the Radioligand Therapy (RLT) Leadership Team to execute on the NIBR RLT drug discovery strategy and liaise closely with NIBR BD&L to evaluate external opportunities. This is an excellent opportunity to join a world class research team at NIBR in Basel, Switzerland. The successful candidate exhibits strong leadership skills, a collaborative team spirit, excellent communication skills and willingness to pro-actively interact across the global organization. Excellent mentoring and coaching skills will be a necessary asset to develop team members scientifically and professionally. Your responsibilities will include: • Lead cross-functional project teams in radioisotope-based therapies • Define and execute on project strategies • Guide, supervise and develop team members across functions • Contribute to clinical development projects within multidisciplinary teams • Works closely with the RLT Leadership Team to execute on the RLT drug discovery strategy • Develop novel ideas and concepts aimed at identifying optimal ways to use cancer drugs, including RLTs/radioligand therapies in patients • Present concepts and projects in a clear, scientifically sound and data-driven, objective manner in different settings and venues • Closely work with multiple teams across expertise groups within Oncology and across departments in the global organization (e.g. BD&L, Global Drug Development, Commercial) 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 • Ph.D. in an Oncology related discipline with strong postdoctoral training and a minimum of 5 years of experience working in the pharmaceutical industry • Strong cancer biology background and track record of scientific accomplishment at high standards and accompanying scientific publications • Track record of successfully leading multi-disciplinary teams including driving novel concepts/projects through all stages of drug discovery • Background in radioligand therapy development/radiobiology is highly desirable • Strong experience in drug development and drug discovery initiatives and projects (including experience with IND-enabling studies), ideally in an industry setting • Proven experience in delivering high level communications and presentations to senior leadership and multidisciplinary teams • Advanced fluency in English (written and verbal) Why consider Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we are 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 is possible, when we collaborate with courage to tackle the world’s toughest medical challenges aggressively and ambitiously. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! *Restrictions on flexible working may apply and will be discussed at interview stages as requiredDivision 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 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 356962BR Nov 24, 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. Novartis’ Comparative Medicine (CM) labs and teams is a key partner with NIBR for advancing in-vivo research through innovation, emerging technologies and biomarkers, while promoting flawless animal wellbeing and science. With excellent clinical care and research model development, CM are advancing NIBR scientific research across the world. CM is now seeking a motivated Senior/Principal Scientist to assume the supervisory role of In-vivo Training Program Lead for the CM in vivo Training & Innovation platform and provide expert advice and teaching opportunities to scientists on state-of-the-art technical approaches. You will be primarily responsible for the alignment of CM Training and Innovation to the organizational direction and needs of the research community, while ensuring outstanding quality, proficiency and efficiency of the program. You will actively propose NIBR scientific groups, novel experimental approaches or technologies to efficiently address in vivo project needs, thus contributing to in vivo research in various research areas within the Novartis Institutes for BioMedical Research (NIBR). Your responsibilities will include: • Primary responsibility for leading the Training and Innovation platform, ensuring highest standards of the training activities, strategic thinking and ability to facilitate complex training activities/lectures, including ensuring the consistency and high quality of the in vivo Training Program including continued review of the program efficiency. • Responsible and active contribution to hands-on activities in the in vivo Training field. • Demonstrate independent judgment to collaboratively implement new technical methods that may impact research projects • Lead and complete independent research requiring highly specialized scientific and technical knowledge • You will be qualified to run a lab or technical platform, including leadership tasks (e.g. managing and running a lab or technical platform and providing regular and fair evaluation of team performance) and able to efficiently manage local/global projects • Maintain compliance with all internal and external regulatory agencies in accordance with the Guide for the Care and Use of Laboratory Animals. You will be required to gain certification and proficiency on all applicable technical skills as required by the job and where applicable • Determining research partner expectations to ensure they are met/exceeded through a proper internal (and external) network • Publish and lecture at internal/external meetings. You will proactively foster regular interaction with other scientists and managers on project activities in other groups and develop and maintain external relationships/contacts. 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: • You will hold either a Doctorate in Veterinary Medicine, a MS, PhD or equivalent (e.g. university degree with extensive industry experience) in scientific discipline such as biology, chemistry or pharmacology with appropriate and relevant years of experience, or apprenticeship (or equivalent) with appropriate and relevant years of experience in drug discovery or another related animal laboratory research • Experience in training programs or advance technical skills in animal research • Accredited or eligible to perform and direct animal experimentation in Switzerland • Leadership/management skills • Superior written and oral communication and data documentation skills required • Working knowledge of federal, state, local (Animal Welfare) laws, departmental SOP’s and Good Laboratory Practices. 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/network *Some restrictions on flexible working may apply and will be discussed at interview as applicableDivision 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 358630BR Nov 22, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With a strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. You will drive the product portfolio and BD&L vision and strategy for Region International, as well as ensure continuous improvement and operational excellence in key processes and systems. Key Responsibilities: • Drives increase in value of new product pipeline across International Region by identifying high-value strategic assets and conducting high-quality primary evaluations across all key criteria established by relevant due diligence guidelines (commercial, product development, technical operations and financial). • Builds robust assessment and forecasting tools to support regional product strategy development, including detailed commercial forecasting and financial valuation models. • Manages commercial due diligence for assigned licensing and acquisition projects. • Develops and monitors relevant key performance indications to capture key Portfolio and BD activities within International Region, provides high-quality insights and recommendations to support growth acceleration and efficiency improvements. • Ensures continuous process improvement and operational excellence across all regional Portfolio and BD activities and systems, by developing and implementing best-in-class processes, providing training, guidance and support to regional and country teams and monitoring ongoing Portfolio and BD activities, to generate insights on potentials areas of process improvements, instil efficiency and ensure compliance with established guidelines and processes. • Ensures continuous team development, increase in productivity and engagement within the Regional Product and BD Strategy & Operations team 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: Essential Criteria: • MSc, MBA or PhD with background in Finance, Economics, Management, Business Administration or Life Sciences • 7+years’ experience in transaction advisory, financial valuation and due diligence roles. • 3+ years’ experience in leading and building high performing teams. • Strong financial modelling and valuations skills and in-depth understanding of main financial valuation methods. • Experience driving large-scale Commercial DD and M&A valuations. • Fluency in English – required; other regional languages desirable (Spanish, Portuguese, Japanese) Desirable Criteria: • CFA certification is preferable 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 Commercial OPS SIR 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 354147BR Oct 26, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. The Data & Analytics organization in IMI is the Novartis engine for achieving best-in-class Healthcare provider (HCP) experience and transformative digital patient engagement. The Customer Experience & Engagement Data & Analytics group seeks a highly motivated leader for global Master Data Management (MDM) capabilities. This role is to enable and govern centralized, multi-tenant MDM capabilities for countries to collaborate, share and co-create data assets for industrialization of analytics & AI. This position reports to the Executive Director, Data Strategy & Governance. The person will be a change agent and evangelize the use of MDM capabilities across all IM markets to drive business value and outcomes. The person will keep abreast of the latest thinking and best-in-class practices for MDM within the industry. MAJOR ACCOUNTABILITIES: • As a leader of the Global MDM capabilities, lead strategy, roadmap, and delivery of multi-tenant global MDM capabilities across global IMI markets • Define, prioritize, harmonize and continuously evolve MDM capabilities by collaborating with Global and Local Data Owners, Insights & Analytics, Customer Engagement and Integrated Marketing leaders • Develop MDM As a Service capability across multiple data domains and maximize re-use of investments by driving harmonization and adoption across local markets • Drive adoption of industry standards and best practices for master data management in the “Glocal” (Global – Local) market. • Define and establish global and local data stewardship policies and guidelines by collaborating with central and local data stewards, data owners and data providers • Establish high trust in master data across the ecosystem by defining end to end process flows, data quality standards and governance models • Collaborate with Legal and Compliance teams to ensure data integrity, data privacy, global and local regulatory needs are met • Collaborate and Manage relationships with data vendors to provide innovation at scale The role can be based in either Switzerland and/or USA. Our selection process will prioritize associates whose roles may be changing or may be impacted as a result of the Transforming for Growth reorganization. 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 will you bring to the role • Bachelor’s degree in Mathematics, Statistics, Computer Science, Engineering, Analytics, Business or other technical degree. Master’s degree preferred • Minimum 10 years of professional experience in Pharma and/or life sciences consulting with progressively increasing responsibility • 2+ years of Experience with working with global teams across multiple geographies • Minimum 3 years of Master data management and/or data management experience with Pharma data • Proven record of cross-functional partnership with other groups such as IT, analytics, global teams #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkNo video provider was found to handle the given URL. See the documentation for more information. Division PHARMA Business Unit Division Management Location Switzerland Site Basel Company / Legal Entity Novartis Pharma 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 354067BR Oct 26, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With a strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. The Data & Analytics organization in IMI is the Novartis engine for achieving best-in-class Healthcare provider (HCP) experience and transformative digital patient engagement. The Customer Experience & Engagement Data & Analytics group seeks a highly motivated leader driving strategy and execution of data products and solutions for Sales Planning management across all IMI markets. This position reports to the Executive Director, Data Products. This role is a thought leader in Sales Planning management and driving data products, enabling reporting & analytics solutions at scale, while generating incremental value for the business. Your responsibilities include, but are not limited to: • Lead strategy and development of data solutions capabilities (e.g., analytical data marts, metric libraries, viz/content delivery tools) related to Sales Planning analytics use cases as Call Planning & dynamic Targeting, Territory, Field Next best actions, Call notes insights • Collaborate with global, regional, and local sales planning teams to develop Analytical Ready Data sets (ARDs) to perform Field Force Analytics and promote sales strategies • Develop data solutions to monitor KPIs and take data driven decisions around Multi-Channel Engagement, Key Account Management planning, Digital assets, and Key Message effectiveness, etc. • Development of IC Grade Data sets to support Goaling and Incentive Compensation processes • Build Analytical Ready Data solutions to integrate reporting with Sales Force Effectiveness to measure field reach, frequency, and field force effectiveness at global scale • Collaborate with field Operations teams to identify new data sets based on the unique commercial models to ensure continuous evolution of analytics use cases related to Field NBA • Partner with Legal and compliance teams to ensure appropriate and authorized use of data sets to meet the regulatory and data privacy laws (GDPR, CCPA, LGPD, POPI, etc.) 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 will you bring to the role • Bachelor’s degree in Mathematics, Statistics, Computer Science, Engineering, Analytics, Business or other technical degree. Master’s degree preferred • 5+ years of professional experience in Pharma data & functions, and/or life sciences consulting with progressively increasing responsibility. • Knowledge of Sales Planning management use cases in a global environment • Expertise in data and analytics related to field NBA • 3+ years’ experience in successfully data/analytics/BI initiatives in industry/consulting setup DESIRABLE REQUIREMENTS: • Excellent understanding of data management platforms (Data Fabric, Data Mesh etc), relational databases systems (RDBMS), data-warehousing concepts, ETL development, and systems integration • Established track record driving business goals and offerings through data, business intelligence, and analytics • Have built and led a data delivery/visual analytics team that has created a data-driven culture #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision PHARMA Business Unit Division Management Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 354051BR Oct 26, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. Novartis’ ambition is to be a recognized leader in customer experience and engagement (CE&E). The CE&E IMI team aims to design and deliver intentional, impactful customer experiences for HCPs and patients through integrated engagements and solutions. The Customer Experience & Engagement Data & Analytics group seeks a highly motivated leader of predictive analytics solutions. This role is turning business needs into analytic initiatives and creating compelling, data-driven narratives based on those analytic outcomes. Accountable for strategizing and executing customer AI products (dynamic targeting, segmentation, and network map of HCPs). The person will keep abreast of the latest thinking and best-in-class methods within the industry. Your responsibilities include, but are not limited to: • Build Customer AI products to support data-driven decision-making by innovatively leveraging data to provide actionable insights on business performance • You will build predictive models to identify and engage with the most valuable physicians • You will drive Customer analytics (e.g. Micro-Segmentation, Patient Prediction models, Lookalike Modeling) and perform A/B tests on content, device etc. across the IMI organization • You will develop optimized channel selection models to identify digital channels and publishers through which Novartis can engage with physicians • You will partner with Integrated Insights and commercial teams to drive Network maps of HCPs based on speciality topics, preferences, and brand lifecycle across key markets and brands • You will collaborate with the Data & AI strategy, Data products, and country Data Science teams to develop customer AI models for micro-segmentation of physicians & patients • Bring a “can-do” attitude and teamwork, and inspire others on culture change • Develop a methodology to measure the impact of the Next best actions • Build models for advanced segmentation and patient identification 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 will you bring to the role • Graduate degree, master's in a quantitative field (Data Science, Engineering, Mathematics, etc.) • 5 years of experience in data analytics, marketing science, or a similar role • 5 years of Pharmaceutical/Biotech/Healthcare in analytics/AI • Experience in Algorithm and product development, a plus with unstructured Data, And / OR Knowledge graphs applications • Good understanding of end-to-end pharma value chain (Discovery, Development and Commercialization process) and experience with field analytics, marketing and sales Analytics DESIRABLE REQUIREMENTS: • Programming experience in Python, R, or a similar language • The high-level initiative, ability to multi-task, and passion for asking and answering questions with large, complex datasets while consistently seeking to innovate • Excellent communication, presentation, and collaboration skills #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision PHARMA Business Unit Division Management Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 353891BR Nov 25, 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. This role can either be based in Basel, Switzerland and//or Boston, USA. Distant working agree-ments may be offered in these locations based on local employment and/or company guidelines. As a result, please note that international relocation or sponsoring from the US to Switzerland or vice versa will not be offered. Within the US, the ideal location for this role is Boston, MA but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide reloca-tion as a result. If associate is remote, all home office expenses and any travel/lodging to specific Boston, MA for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require some travel. Your responsibilities include, but are not limited to: Drive Portfolio Strategy and decision making: • Support definition and delivery of mid-and-long term portfolio strategy, goals, strategic objectives and leadership aspiration within TA and DAs in collaboration with other functions within S&G and in IM, GSPC, GDD, & NIBR. Help drive stakeholder alignment around updates to the strategy as needed, e.g., due to internal or external market events • Identify potential pipeline gaps and make recommendations to address with other S&G functions, IM, GDD and NIBR partners • Collaborate closely with key stakeholders (e.g., GPSC, IM, NIBR, GDD, local functions such as Market Access & Pricing) to facilitate portfolio decision making in the context of our goal of becoming a top 5 Pharma player in the US while maintaining our international leadership • Support assessments of programs fit to current portfolio strategy, and drive content development to facilitate portfolio prioritization / de-prioritization / trade-off discussions for Innovation Management Board (IMB) • Support DA strategic insights development and forecasting, including Forecasting Consortium challenge sessions for programs prior to IMB review Optimize the early-stage TA portfolio • Support forecasting, commercial viability, unmet needs (esp. US), evidence strategy and LCM considerations to inform NIBR product strategy, including identification of key data requirements to support transition of assets to DDP / FDP (Development Decision Point / Full Development Decision Point) • For assets post DDP/ FDP that have transitioned to the GPT, work in collaboration with GPSC lead to optimize sequencing of additional lifecycle indications and develop proposals for IMB review Provide external perspective and identify growth opportunities: • Provide commercial input into BD&L, triage opportunities, review non-confidential information and decision making for evaluations and conduct market research together with Insights and Analytics for opportunity sizing and business case preparation. Drive strategic insights and outside-in challenge of internal assumptions around core pipeline and external opportunities (e.g., forecast assumptions) and within key portfolio governance processes. Support white space exploration with Novartis Strategy and diligence and external landscape mapping with BD&L and M&A •Support commercial discussions on partnering opportunities for internal and external portfolio with top Pharma companies, support commercial DD activities and synthesis of commercial recommendations. Support Licensing and Merger and Acquisition commercial evaluations • Assist Group Investor Relations and the CEO Office with dissemination of key strategic insights Others: • Provide support to the broader TA Strategy Group in helping challenge and develop other TA Strategy Directors Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Advanced degree (PhD, MD, or other advanced University degree) or equivalent experience in life science/healthcare; MBA, consulting, or equivalent experience highly desirable • In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) • Highly agile having the capacity to support several strategic DAs within a TA and multiple programs internal and external • Substantial experience evaluating new product opportunities through M&A, BD&L, and internal re-search programs • At least 5-7 years of pharma industry and/or medical device experience in Research & Development and/or commercial functions with experience conducting, commissioning, and analyzing primary re-search • Experience of strategy development and asset shaping early in lifecycle (any functional perspective) • Recent (post 2015) local US experience preferred; local US experience includes working within the US market with the local US customers, US health care systems / systems of care, US payors / ac-counts, etc. and driving US market strategy • A track record of supporting areas such as Commercial, Medical Affairs, Market Access, as well as Business Development & Licensing • Ability to comfortably engage with senior leadership to influence and challenge with excellent inter-personal skills • Strong financial modeling and assessments for valuation skills and experience in strategic and competitive data analysis and insights generation, leveraging digital tools • Strong communication, consensus building, and influencing skills • Enterprise maximization mindset in balance with TA needs: able to align to broader enterprise strategy for trade-off against shorter-term payoffs to avoid unnecessary investments. Desire to make bold choices to stop/ divest/ reduce investment Strategic collaboration and cross functional leadership; effectively work in matrix balancing cross-functional perspectives and alignment with business priorities against flexible resourcing #transformingforgrowth Why Novartis? 766 million. That’s how many lives our products touched in 2021 and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis Imagine what you could do at Novartis! Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] let us know the nature of your request and your contact information. Please include the job requisition number in your message Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network We are Novartis. Join us and help us reimagine medicine.Division CORPORATE Business Unit Group Corporate Affairs & Global Health Location Switzerland Site Basel Company / Legal Entity Novartis International AG Alternative Location 1 USA Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 358462BR Nov 23, 2022 Switzerland Job Description Over 190! That’s the monthly number of requests from associates who were seeking insurance protection for themselves and their families. At Insurance Services Novartis, we like to think outside the box and challenge the status quo. We take an optimistic approach by focusing on the positives and creating solutions that will improve and secure employees and their families’ optimal protection in their life. Novartis provides its associates with an independent and free consulting service for insurance matters. Together with an independent provider, we select the providers in order to offer our associates optimal insurance coverage with advantageous conditions. Your Responsibilities: • Competent and correct provision of information on all aspects of insurance and pensions • Training and instruction for the people partner team, information for insured people (e.g. Welcome Days) as well as technical training and participation in and execution of lunchtime events • Provide competent and correct advice and support for employees on all insurance issues, as well as for active employees and pensioners during and after retirement (including surviving dependents) on all pension fund-related issues. If necessary, involve other internal or external partners (e.g. AHV, IV, social counselling, tax administration, cross-border commuter organizations etc.) • Manage administrative tasks like processing company exits, retirements, suspensions, reactivations, deaths, interns as well as premium collection, account assignment, e-banking for accounting and assistance with website maintenance • Process and execute as a pension fund advisor (25%) with an assigned portfolio of asset and retiree mutations, e.g., new additions, vested benefits, purchase calculations, part-time changes, divorce calculations, and administrative processing of divorce-related departures, service terminations, fund changes, administrative mutations, etc. • Close, case-related cooperation, coordination, discussion and advice with social service, HR services, authorities (AHV, IV) and line to optimize business processing 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 commercial training (e.g. KV apprenticeship or commercial school) or equivalent (e.g. other apprenticeship; has very good administrative knowledge/experience) • Further training in the field of insurance or social insurance (e.g. professional certificates or diplomas, Verwaltungsfachschule Olten), diploma as an Versicherungsvermittler VBV is an advantage • 5+ years of professional experience in the field of insurance and/or occupational pensions • Experience in dealing with insured persons and their concerns • Proficiency in English and German (written and spoken) Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision CORPORATE Business Unit GROUP PEOPLE & ORGANIZATION Location Switzerland Site Basel Company / Legal Entity Pensionskasse Novartis Functional Area Human Resources Job Type Part Time Part Time percentage 50 Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 353890BR Nov 25, 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. This role can either be based in Basel, Switzerland and//or Boston, USA. Distant working agree-ments may be offered in these locations based on local employment and/or company guidelines. As a result, please note that international relocation or sponsoring from the US to Switzerland or vice versa will not be offered. Within the US, the ideal location for this role is Boston, MA but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation as a result. If associate is remote, all home office expenses and any travel/lodging to specific Boston, MA for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position will require some travel. Your responsibilities include, but not limited to: Drive Portfolio Strategy and decision making: •Define and drive mid-and-long term portfolio strategy, goals, strategic objectives and leadership aspiration within TA and DAs in collaboration with other functions within S&G, GPSC, IM International, IM US, GDD and NIBR. Orchestrate stakeholder alignment around updates to the strategy as needed, e.g., due to internal or external market events • Identify potential pipeline gaps and make recommendations to address with other S&G functions, IM, GDD and NIBR partners • Collaborate closely with key stakeholders (e.g., GPSC, IM, NIBR, GDD, local functions such as Market Access & Pricing) to facilitate portfolio decision making in the context of our goal of becoming a top 5 Pharma player in the US while maintaining our international leadership • Lead assessments of programs fit to current portfolio strategy and drive content development to facilitate portfolio prioritization / de-prioritization / trade-off discussions for Innovation Management Board (IMB) • Own DA strategic insights development and forecasting, including co-leading Forecasting Consortium challenge sessions for programs prior to IMB review Optimize the early-stage TA portfolio • Serve as NIBR DA commercial lead, providing clear direction on asset portfolio strategic fit, and guiding very early asset shaping, including forecasting, commercial viability, unmet needs (esp. US), evidence strategy and LCM considerations to inform NIBR product strategy. Identify key data requirements to support transition of assets to DDP / FDP (Development Decision Point / Full Development Decision Point) • For assets post DDP / FDP that have transitioned to the GPT, work in collaboration with GPSC lead to optimize sequencing of additional lifecycle indications and develop proposals for IMB review • Support fail-fast approach to ensure timely closure of non-priority assets and resources re-allocation for new priorities Provide external perspective and identify growth opportunities: • Provide commercial input into BD&L, triage opportunities, review non-confidential information and decision making for evaluations and conduct market research together with Insights and Analytics for opportunity sizing and business case preparation. Drive strategic insights and outside-in challenge of internal assumptions around core pipeline and external opportunities (e.g., forecast assumptions) and within key portfolio governance processes. Drive white space exploration with Novartis Strategy and diligence and external landscape mapping with BD&L and M&A • Lead commercial discussions on partnering opportunities for internal and external portfolio with top Pharma companies. Leads, in partnership with IM, the commercial DD activities and synthesize commercial recommendations. Leads, in partnership with IM, Licensing and Merger and Acquisition commercial evaluations • Assist Group Investor Relations and the CEO Office with dissemination of key strategic insights Others: • Provide leadership support to TA Strategy Directors in developing value proposition and recommendations for key milestones (e.g., DDP, FDP) on projects in the TA • Coach and develop more junior talents within the group Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Advanced degree (PhD, MD, or other advanced University degree) or equivalent experience in life science/healthcare; MBA, consulting, or equivalent experience highly desirable • In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) • Highly agile having the capacity to manage several strategic DAs within a TA and multiple programs internal and external • Substantial experience evaluating new product opportunities through M&A, BD&L, and internal re-search programs • At least 10-12 years of pharma industry and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, and analyzing primary research • Experience of strategy development and asset shaping early in lifecycle (any functional perspective) • Recent (post 2015) local US experience preferred; local US experience includes working within the US market with the local US customers, US health care systems / systems of care, US payors / accounts, etc. and driving US market strategy • Recent (post 2015) experience in global role preferred • A track record of successfully working with Commercial, Medical Affairs, Market Access, as well as Business Development & Licensing • Ability to comfortably engage with senior leadership as well as mid-career associates to influence and challenge with excellent interpersonal skills • Strong financial modeling and assessments for valuation skills and experience in strategic and competitive data analysis and insights generation, leveraging digital tools • Strong strategic vision and excellent communication, consensus building and influencing skills • Enterprise maximization mindset in balance with TA needs: able to align to broader enterprise strategy for trade-off against shorter-term payoffs to avoid unnecessary investments. Desire to make bold choices to stop/ divest / reduce investment • Strategic collaboration and cross functional leadership; effectively work in matrix balancing cross-functional perspectives and alignment with business priorities against flexible resourcing #transformingforgrwth Why Novartis? 766 million. That’s how many lives our products touched in 2021 and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis Imagine what you could do at Novartis! Accessibility and accommodation Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network We are Novartis. Join us and help us reimagine medicine.Division CORPORATE Business Unit Group Corporate Affairs & Global Health Location Switzerland Site Basel Company / Legal Entity Novartis International AG Alternative Location 1 USA Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 357305BR Nov 08, 2022 Switzerland Job Description More than 2 million compounds are managed by the compound management teams at the Novartis Institute for Biomedical Research (NIBR). 20+ highly skilled and motivated logistic experts and engineers provide 5000+ scientists with effective access to these compound samples enabling drug discovery at NIBR. Together with our colleagues in NIBR informatics and external lab automation providers, we build, maintain and operate highly automated compound storage, ordering, handling and distribution processes and systems for hit finding and lead optimization at global scale fulfilling 1000+ orders every day. The compound management team is looking for an experienced automation and IT-expert to co-lead the development of our next generation set-up for compound lead optimization and hit finding. As the Program Manager, It Process & Automation, you will co-design, document and manage the implementation of new processes and systems for compound sample handling as well as work closely with our logistics experts in our labs to maintain and improve our existing systems. This role requires frequent and flexible on-site presence in our compound management labs. The role is based in our NIBR research sites Basel, Switzerland or potentially in Cambridge, USA. You are a self-motivated, curious, creative and agile technology expert and leader with strong communication skills, who enjoys working in a collaborative, fast-paced environment and wants to positively impact drug discovery through information and automation technologies. Your key responsibilities included, but are not limited to: • Designing, documenting and managing the implementation of automated logistics processes and systems within a complex, global IT- and automation environment. • Building a deep understanding of the NIBR compound logistics infrastructure and processes • Leading, conduct and document process business analyses including process and IT-integration design, identifying gaps and inefficiencies in current set-up and developing comprehensive requirement specifications including cost, time and resource estimates • Engaging with global colleagues to develop and align on a long-term compound management system integration strategy and roadmap • Leading the full development cycle from system definition, prototyping & testing to production release whilst working closely with the solution provider • Challenging the status quo, improving operations, processes and enabling continuous optimization of our workflows • support the compound management team members in day-to-day operations with IT-issue resolution, issue ticket writing and testing • Providing leadership, mentoring and training for team members in the application of the best standards practices for business analysis, process and IT-integration Learn how your work can make an impact here! 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 need: • A MSc Degree with extensive experience in several of the following areas: computer sciences, automation or process engineering, process business analysis, lean management, technical project management, sample logistics, drug discovery sciences • Significant experience managing complex software development and IT project integrations • Proven track record in translating business needs into clearly defined technology product implementation roadmaps • Extensive experience with project management and documentation tools: MS-project, Lucidchart, JIRA, Confluence or equivalent tools • Experience with automated data handling, software architecture, transactional databases, web service architecture and software development • Excellent ability to communication with senior leaders in a matrixed working environment with a customer focused, solution oriented approach • Proficiency in English (written and oral) Why consider Novartis? 769 million. That’s how many lives our products touched in 2022. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! 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 We are Novartis. Join us and help 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 354063BR Oct 26, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. The Data & Analytics organization in IMI is the Novartis engine for achieving best-in-class Healthcare provider (HCP) experience and transformative digital patient engagement. The Customer Experience & Engagement Data & Analytics group seeks a highly motivated leader to enable & scale best-in-class multi-tenant data hub for IMI organization. This position reports to the Executive Director, Data Strategy & Governance. The person will be a change agent and evangelize the use of Data Hub capabilities across all IM markets to drive business value and outcomes. Your responsibilities include, but are not limited to: • Responsible for implementing & scaling centralized multi-tenant data-hub to host commercial, patient services, market access, digital & Next generation data & it’s products and services across Novartis IMI countries • Define, prioritize, harmonize and continuously evolve data hub capabilities by collaboration with both global functions/ teams and countries • Drive adoption of industry standards and best practices for data hub/ data management in the “Glocal” (Global – Local) market • Establish high trust in data across the ecosystem by defining end to end process flows, data quality standards and governance models • Collaborate and Manage relationships with data vendors to provide innovation at scale 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 will you bring to the role • Bachelor’s degree in Mathematics, Statistics, Computer Science, Engineering, Analytics, Business or other technical degree. Master’s degree preferred • Minimum 5 years of professional experience in Pharma and/or life sciences consulting with progressively increasing responsibility • 2+ years of Experience with working with global teams across multiple geographies • Minimum 3 years of data management/ data hubs experience with Pharma data • Proven record of cross-functional partnership with other groups such as IT, analytics, global teams #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. 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 PHARMA Business Unit Division Management Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 354058BR Oct 26, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but continue to allow us to bring innovative medicines to patients quickly. The Data & Analytics organization in IMI is the Novartis engine for achieving best-in-class Healthcare provider (HCP) experience and transformative digital patient engagement. Your responsibilities include, but are not limited to: • Build & lead next-gen Data Capabilities to support Data Acquisition, Data Management, and Launch Excellence with automated governance that can scale for global and local needs • Enable Robust Data Quality, catalogue & data operations framework that supports diverse needs of each country while templatizing process-aware automation and early detection of issues • Drive adoption of modern data & analytics enablement using ARDs, MRDs and RRDs by upskilling user communities through rich training, documentation, and iterative improvements • Integrate and scale AI capabilities to optimize data & analytics operations, governance & adoption for ‘glocal’ (global & local) communities • Drive execution and adoption of Data & AI Quality standards across IMI markets to ensure that our next-generation capabilities evolve to support future Novartis Innovative Medicine’s objectives • Partner with Ethics, Legal and Compliance to ensure data integrity, compliance to global regulatory standards and privacy policies across geographies (GDPR, CCPA, POPI, LGPD, etc.) 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 will you bring to the role • Bachelor’s degree in Mathematics, Statistics, Computer Science, Engineering, Analytics, Business or another technical degree • Minimum 5 years of professional Experience in Pharma and or life sciences consulting with progressively increasing responsibility • 2+ years of Experience working with global teams across multiple geographies • Minimum 3+ years of Data Strategy, Data Governance and/or Data management experience with Pharma data • Proven record of cross-functional partnership with other groups such as IT, analytics, global teams, and local country partners #transformingforgrowth Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we're proud of this, we know there is so much more we could do to help improve and extend people's lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. 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 PHARMA Business Unit Division Management Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area BD&L & Strategic Planning Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

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

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

Job ID 357141BR Nov 24, 2022 Switzerland Job Description New modalities and especially oligonucleotides play an increasing role in the Novartis project pipeline and thus call for the development and implementation of novel analytical methods, as well as cutting-edge data analysis workflows. We are looking for a highly motivated Postdoctoral candidate with a strong background and experience in Data Science applied to Analytical Chemistry. This position offers a unique opportunity to shape the applied analytical science of Oligonucleotides at Novartis. In parallel to your Postdoctoral activities, you will receive outstanding insights into drug development at Novartis and shape your network for the next career step. State-of-the-art equipment and science paired with a highly dynamic, multicultural, and committed team of scientists is granted. Are you interested? We are waiting for you to put your own stamp on it. The position is located at the Novartis Headquarter site in Basel within the Analytical R&D (ARD), which is a line function of the Technical R&D department of Global Drug Development. ARD plays a crucial role in the characterization and analysis of Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. Timing: 2023 (preferred start date February 2023) Duration: 12 months Your responsibilities: • Identify, evaluate and implement data analysis tools based on multivariate data analysis and statistics for chromatographic raw data extraction, collection, and evaluation. • Develop methodologies based on machine learning to model the data and enable automated data processing of chromatographic methods. • Implementation of the automated workflows to accelerate development timelines. • Present your research internally and at international conferences to build an external network and constantly evaluate the external landscape in this field. 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: • Recently finished PhD in analytical chemistry or related discipline, with interest and experience in data science, applied statistics or related subject area. • Strong experience in programming tools (i.e., R, Python), machine-learning algorithms and sophisticated digital skills. Expertise with some publishing models and in chemometrics with regards to automated method development, signal processing / recognition is an asset. • You bring along analytical knowledge and experience in chromatography and mass spectrometry methodologies. Experience with Chromeleon would be desirable. • An excellent track record of original research in analytical chemistry and data science applications demonstrates your strong background in the above-mentioned fields. • While you are a strong team player and role-model in collaboration, the ability to work independently will be valued. • You have a creative mindset, self-driven attitude, high level of learning agility and are constantly eager to expand your knowledge and establish new techniques. • A track record on strong interpersonal and communication skills is regarded as a basic requirement. 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!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 358192BR Nov 22, 2022 Switzerland Job Description Novartis Institutes for BioMedical (NIBR) is the global pharmaceutical research organization of Novartis. With approximately 6,000 scientists and physicians around the world, our research is focused on discovering innovative new drugs that will change the practice of medicine. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies. At NIBR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need ground breaking, pioneering computing systems. The Associate Director, Portfolio Operations and Planning Analyst will help our NIBR Informatics (NX) team to deliver the highest value to our scientists within a reasonable cost. The team defines its single strategy and realize it through fully integrated portfolio and supports product and service delivery through solid planning, delivery, monitoring and measurement of results. Your responsibilities include but are not limited to: • Creating and operating an Adaptive Portfolio Management process for NX Products, Services and strategic Programs • Collaborating across NX to develop a Road-Mapping process as the main tool for long term planning of our Portfolio • Supporting NX leaders in strategic level portfolio planning for non-scientific business developments • Works side-by-side with SPM/ Portfolio operations to deploy, operate and continuously evolve processes, forums, documentation, tools used in the process • Collaborating to translate desired strategic outcomes to strategic change Programs in the Portfolio. Facilitating resource prioritization and organisational change processes related to Strategic programs and material changes in Portfolio in general (beyond scope of a Product line) • Working with our Business Planning & Resource Fulfilment teams to support Business Planning and to integrate NX budget and related aspects into Portfolio selection and commitments • Working with NX Delivery Excellence to assess feasibility of delivery of planned Portfolio outcomes and to assess complexity of planned activities • Striving for lean processes that enable independent decisions of empowered teams, that facilitate planning of teams downstream from these decisions and that brings holistic/ up-to-date view of NX Portfolio to NX and our business leaders • Working in close collaboration with Business Performance and with IT Product teams to develop/ acquire and deploy tools that enable fast decisions based on high quality of data owned by NX teams Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What You'll Need: - Degree in Life Science or Technology or equivalent relevant experience in related fields - Strong experience working in a technology Life science organisation or Product organisation targeting technology Life science market - Solid experience managing teams accountable for business outcomes in a direct management or Project/ Program management role and - Formal training in Project/ Program and Portfolio management - Good understanding of IT, Informatics organisations and the scientific research process - Proven ability to think conceptually and communicate effectively with senior business leaders to deliver in uncertain, ambiguous, complex environments with high level of change - Proficiency in English (Oral and written) - Ability to travel 25% Nice To Have: - Proven success with implementation and operation of Product/ Program Planning processes in a Product organization strongly preferred - Proficiency in Germany (oral and written) Why consider Novartis? 769 million. That’s how many lives our products touched in 2022. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! 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 (https://talentnetwork.novartis.com/network) We are Novartis. Join us and help reimagine medicine. Commitment to Diversity and 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. 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. OVID-19: 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]Division NIBR Business Unit CBT - NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 355717BR Nov 21, 2022 Switzerland Job Description Novartis Institutes for Biomedical Research (NIBR) is the global pharmaceutical research organization of Novartis. With approximately 6,000 scientists and physicians around the world, our research is focused on discovering innovative new drugs that will change the practice of medicine. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies. At NIBR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems. With NIBR Informatics (NX), NIBR is making a strategic investment into informatics capabilities and is positioning itself to deliver the systems and services that are critical to the future of drug discovery. About the department The Software Engineering (ENG) group in NX applies excellence in Engineering to build impactful software and data products that enable advanced scientific development at NIBR. We partner with the Software Product organization to deliver intuitive, intentional, and integrated software solutions that create a frictionless user experience. The Clinical Product Line primarily supports translational research and early clinical development. Purpose of the Role As Engineering Lead you will partner closely with your co-lead, the Product Line Manager, to define and realize the product and technical strategy for the Clinical Informatics Product Line. You will provide technical guidance to co-create a vision for a group of globally deployed, high-impact scientific software products essential for NIBR clinical operations. This will require a deep knowledge of technology and processes within translational research and early clinical development. In collaboration with the NX organization you will contribute to a well-engineered, integrated, capability-based product landscape. As a hands-on technical leader, you will also contribute directly to the design and implementation of key products within the Clinical Product Line. Major accountabilities & key activities Your accountabilities include: • Develop an architectural vision for the Clinical product line. • Align technical interfaces of NX products and late-stage clinical development • Structure internal and external resources on the Clinical product line. • Identify and remove technical roadblocks. • Champion software development best practices. • Lead development of a key clinical product. 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 Experience Requirements (Core Skills and Capabilities): You bring relevant technical leadership and engineering experience in complex business environments, as well as domain expertise in translational research and early clinical development in the drug discovery industry. Your experience demonstrates the following qualities: • Able to inspire and enable bold innovation in GxP and clinical products • Solution oriented; proactive and action oriented • Curious, open, and willing to learn • Holds self and others to high technical standards Education and Qualification Requirements: • BS/MS in Computer Science, Informatics or similar, or equivalent practical experience • 8+ years of hands-on software development experience Technical Competencies: The following technologies are used within the clinical product line. The successful candidate will understand the effective application of many of them. • AWS • Oracle Apex • Docker • Java • Python • JavaScript o Node.js o React o jQuery 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 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 354540BR Oct 24, 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 NIBR Biologics Centre (NBC), in collaboration with the disease areas and technical expert groups, builds the future biologics therapy pipeline of Novartis through the discovery and creation of new antibody, protein, nucleic acid and virus-based molecules. In your role as Senior Scientist II, you will support the antibody discovery within a group in NBC in Basel, Switzerland. We are looking for an experienced, creative, and motivated team player. You will be part of a team responsible for the discovery of world leading therapeutic antibodies. Here you will work independently with various technologies like phage display, mammalian display to discover antibodies followed by their bio-chemical and functional characterization. Your responsibilities will include, but are not limited to: • Apply multiple cutting-edge selection techniques to synthetic and immune antibody libraries, like phage display, mammalian display, FACS sorting, plate-based screening. • Analyse and screen selection outputs by Next Generation Sequencing (NGS). • Sub-clone hits into expression vectors and produce them at micro-scale in a high-throughput manner. • Characterize binders’ properties in various affinity and activity assays, like ELISA, FACS, Octet, epitope binning, reporter gene assays. • Engineer and improve binders by mean of affinity maturation or humanization. • Generate hypotheses to test, troubleshoot issues, design, and execute the next set of experiments. • Document the results in a detailed manner in laboratory journal and in internal databases. • Present research updates and participate constructively in working project teams and at laboratory group meetings. • Be part of a team of 3 scientists reporting to a lab head. 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 in Biological or Biochemical Sciences with 5+ years of laboratory experience or recent PhD with 1-2 years of laboratory experience. • Ideally 2-5 years of industry experience, in antibody discovery technologies, including at o least one technology like phage, yeast and/or mammalian display. • Good experience in flow cytometry analysis as well as sorting is mandatory. • Knowledge in antibody engineering is a plus. • Solid background in molecular biology, bacterial and mammalian cell biology, biochemistry, affinity, and activity assays. • Hands- on experience with data management and sample storage system. • Excellent oral and written communication in English and interpersonal skills. • Self-motivation, enthusiasm, and scientific curiosity. What Novartis can offer you? In addition to outstanding benefits and competitive salary, you will: Be part of a team that is generating high quality therapeutic antibodies to help patients. Gain experience with a variety of cutting-edge antibody selection and screening techniques. Work with the latest technologies and instrumentation. Be part of a world-class organization dedicated to providing solutions to un-met medical needs. Join an organization that is committed to your development and advancement. Why consider Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we are 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 is possible, when we collaborate with courage to tackle the world’s toughest medical challenges aggressively and ambitiously. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! *Restrictions on flexible working may apply and will be discussed at interview stages as requiredDivision 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 353752BR Nov 21, 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 Novartis ambition is to be a recognized leader in customer experience and engagement (CE&E). The CE&E IMI team endeavors to design and deliver intentional, impactful, and connected customer experiences for HCPs and patients through integrated engagements and solutions. As part of our MarTech Platforms product team, the Executive Director (ED), Web Assets will develop, identify, and prioritize web based digital solutions, related integrations, and innovation to enable our current and future state business priorities. This role is part of the MarTech Platforms team of the CE&E, IMI organization - a team focused on driving the tech platform/products strategy and developing strong above-country interface and partnership for product platforms and release roadmaps. You will be responsible for ensuring that the IMI website ecosystems and assets globally are effective and providing an excellent customer experience. The successful candidate be fluent in strategy and operational web-site planning by blending creative, technical and analytical skills to integrate and enhance our medical and commercial websites as an anchor in our customer experience landscape. This is a customer centric role, working to translate the needs of the customer into online business opportunities. In this role, you will have a customer-first mindset, a strong understanding of back-end and front-end website product platforms, and the ability to integrate data and analytics that can be used to track, analyze, and improve our websites. This role requires a candidate with excellent analytical, organizational, and communication skills as you'll be working with a team to interpret technical and business requirements as well as data. This role can either be based in Basel, Switzerland and/or New Jersey, USA. Distant working agreements may be offered in these locations based on local employment and/or company guidelines. As a result, the relocation or sponsoring from the US to Switzerland or vice versa will not be offered. Within the US, the ideal location for this role is New Jersey, but remote work may be possible (there may be some restrictions based on legal entity). Please note that this role would not provide relocation. If an associate is remote, all home office expenses and any travel/lodging to specific New Jersey sites for periodic live meetings will be at the employee’s expense. The expectation of working hours and travel (domestic and/or international) will be defined by the hiring manager. This position may require a certain amount of travel. Your responsibilities include, but not limited to: • Manage a team of three: CMS and CPM (Consent and Preference Mgmt.); Next Gen Web; and Web-site Product Owner / Manager • Develop and deliver the website roadmap, user experience strategy, and 3-5 year tech/opps roadmap. Partner with CE&E Operations to ensure resource and investment forecast, budget, and spend. • Architect a unified website ecosystem strategy and user experience, identifying the role and connectivity for our IMI websites including events, patient disease management sites, clinical trial and recruitment sites, and HCP portals. This includes defining the role and connectivity of the website versus/with other digital channels including social media, HCP events, Search, mobile, and patient sup-port solutions. • Ensure the efficient and effective, best in class scale of our website product to our markets with reduced complexity and user experience excellence. To achieve this, the ED role will support and guide the: o Director, Next Gen Web in defining the future state for our website ecosystem including sequencing of related features and functionality and supporting CX/Content strategy and operational plan. o Website product owner in establishing content governance and planning process with CX team, as well as data-led prioritization of website enhancements, features, and functionality with IT and markets o Director, CMS and CPM in effective and efficient management for in-house DRUPAL, CMS, and CPM technical products including aligning on an overall integration sequence and plan for our global sites • Work with team to define KPIs, reporting, and analysing marketing automation performance. Create recommendations to improve platforms, process, and capabilities • Create and manage overarching website governance process in line with Global Risk, Privacy, and Compliance processes aligned with IT current processes and SOPs • Develop strong above-country interface and partnership with DD & IT (Data and Digital & Information Technology) for above including ROI, resource, and investment forecasts • Develop internal communication and change management plan to clarify roles, responsibilities, and integrated planning / progress, partnering across IT / SMEs, business leads, markets and key stake-holders. Ensure clarity in ways of working (WoW) with market BE&E groups in execution. • Be an evangelist, thought leader, and change agent in website excellence including external trends; enable a cohesive community of practice across Novartis IMI that is scaling knowledge and technology effectively and operating with consistent and reliable executional excellence • Excel in process and planning efficiency to decrease complexity and internal burden in execution • Assess and manage 3rd party agency, vendor, and outsourced/contract talent for, and with, 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: • 8-10 years + experience in developing E2E globally scaled website solutions and services to support end to-end business performance, with demonstrated results • Deep SME in website technologies / integrations (e.g., Drupal, CMS, CPM, etc.), user experience, platforms, and data requirements • Ability to understand and co-lead the technical platform integrations and requirements process needed to drive a compliant, competitive approach for the enterprise • Previous Platform / Product Owner experience with demonstrated results • Experience in platform strategy and management; ability to deliver solutions against the Agile methodology and to integrate platforms and technologies into core business processes and standards Desirable Requirements • Ability to act as SME and change champion: develop and drive new website standards and governance across IMI • Drive innovation: through platforms, predictive content modeling (e.g., SFMC), and AI/ML insights • Fluent in adjacent or connected digital channels: Social, Search, Mobile, Events, Email/CRM, etc. #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. 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. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to tackle the world’s toughest medical challenges aggressively and ambitiously. 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!Division PHARMA Business Unit Division Management Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 USA Functional Area Marketing Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 351333BR Oct 27, 2022 Switzerland Job Description 5600 scientists working on 340 discovery programs in 8 disease areas focusing on 90 new molecular entities makes Novartis the premier place to develop your career as a pharmaceutical professional. If you are curious, scientifically minded, and want to positively impact society by speeding delivery of novel therapies to needy patients, then look no further, NIBR is the place to be. In the role of Therapeutic Area (TA) Head, Autoimmunity, Transplantation & Inflammation (ATI) Preclinical Safety (PCS) you will be responsible for delivering the safety assessment strategy and scientific excellence for the ATI disease area within Preclinical Safety. You will drive the strategy and oversee the implementation of preclinical drug development activities, and all scientific activities within PCS to ensure optimization/maintenance/issue resolution re. to the R&D portfolio. As a globally recognized senior preclinical expert you will lead the PCS TA strategy team comprised of drug development experts to ensure optimal support of R&D projects in terms of science, quality and timeliness. Your main accountabilities will be: • Responsible for preclinical safety assessment and development strategy of PCS TA. Contribute to global PCS strategy on safety assessment and drug development. • Provide expert leadership and accountability for coordinated scientific and operational review of: o Preclinical Development Plan(s) and Safety Profiling Plan(s) (SPP) o PCS regulatory documents (IB, IND, CTD, BBs, HA questions, etc.) o Study Protocol synopses o New study designs/ endpoints/ biomarker strategies for disease area o Innovative within and cross project data utilization o Innovative technologies/ drug development approaches More specifically you will: • Provide thought leadership and lead continuous improvement in safety assessment strategies and project support in the TA and contribute to same in global PCS. • Provide expert input into due diligence assessments of potential licensing and acquisition projects and provide review of preclinical due diligence reports for the TA. • Oversight of all preclinical development activities (including timelines) for all projects managed by the PCS TA from NTRC to phase IV programs. Oversight of resources planning for DA (Ex-POC) and DF (Phase 2-marketing) Basel location preferred for this role. 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: The ideal candidate will possess a PhD in pharmacology, toxicology or a related biological science; MD with appropriate experience, DVM with appropriate training and experience. PharmD or equivalent with a strong biological background or equivalent work experience. Desired Experience: • 5 plus years’ experience in a nonclinical safety scientific discipline (e.g. Study Director, Study Monitor, Study Pathologist, Investigative Toxicology) • Minimum of 10 years’ experience as a full-time nonclinical safety PTM (regulatory stage projects, in Novartis or in a similar organization ex-Novartis) • Ability to mentor others in nonclinical safety issue resolution • Ability to communicate (written and verbal) and negotiate with Health Authorities on complex issues 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/network DivisionDivision 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 345794BR Dec 02, 2022 Switzerland Job Description Bringing life-changing medicines to millions of people, Novartis sits at the intersection of cutting-edge medical science and innovative digital technology. As a global company, the resources and opportunities for growth and development are plentiful including global and local cross functional careers, a diverse learning suite of thousands of programs & an in-house marketplace for rotations & project work. With strong medicines pipeline our current transformation will not just deliver growth for our business but con-tinue to allow us to bring innovative medicines to patients quickly. We are looking for a Senior Manager - Internal Audit who will be a trusted partner for the business to improve governance, risk management, processes and our culture. You will get to engage with senior leaders of Novartis corporate functions and country organizations. You will also be able to further develop your skills and strengths that will help you to reach new heights in the profession in an inspired, curious and un-bossed organization. Your responsibilities include, but not limited to: • Plan, deliver and follow up from assurance and advisory projects in the markets and at the corporate level either as a team lead or team member. • Identify the root causes of audit findings and investigate, analyze and recommend practical solutions to prevent re-occurrence. • Act as a cultural change agent, supporting assurance function with business partnering. • Support the audit team by providing peer-to-peer coaching and training, as well as, on-boarding new team members. • Manage knowledge and drive innovation to ensure high-quality, value-adding and digitally enabled audit execution. • Contribute to the digital transformation of the audit function to leverage the opportunities presented by current and new technologies and data across the organizations. • Contribute to regional or global Internal Audit methodology projects and continuous improvement initiatives. • Build and maintain key relationships with stakeholders, establishing a culture of engagement while adding value. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements • 6 plus years' experience working in an internal audit department of an international company preferably in Pharma, medical devices, or Biotech sector OR a minimum of 10 years of experience in the business (e.g. commercial, general management, Finance) with a strong interest in internal audit • Good knowledge of SAP FI and CO modules, ACL, Tableau, Excel or other audit tool • Strong business acumen and knowledge of process management and/or business process optimization • Team-player with project management skills to collaborate effectively across a matrix • Ability to prioritize assignments, deal with interruptions, and meet deadlines in a fast paced and growth-oriented environment • Excellent communication and interpersonal skills including the ability to interact effectively with a wide variety of departments and leaders at all levels of the organization. • Strong analytical skills and ability to process and analyse large data size to identify trends and exceptions together with a positive attitude, pro-active and resourceful. • Proficient in English plus at least one other language desirable, like Russian, French, German, Spanish, or any Eastern European. Willingness to travel up to 30% 766 million. That’s how many lives our products touched in 2021 and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis Imagine what you could do at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network We are Novartis. Join us and help us reimagine medicine.Division CORPORATE Business Unit BUSINESS ASSURANCE AND ADVISORY Location Switzerland Site Basel Company / Legal Entity Novartis International AG Functional Area Audit & Finance Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 359373BR Dec 02, 2022 Switzerland Job Description 80 million! This is the number of pre-filled syringes, vials and ampoules that are produced every year in Steriles at our plant in Stein and delivered as medicines to more than 150 countries. For the Engineering Packaging team we are looking for a motivated and committed intern for 6-12 months, who will get in close touch with our highly automated Packaging Lines for our High-Quality-Pharmaceutical Syringe-Devices and Vials-Kits. Preferred start date: February / March 2023 Latest start date: September 2023 Duration: 6-12 month Your responsibilities will include: • Support Plant Engineers in their daily work on the shop floor and with their assigned projects. • Efficiently collaborate and interact with Plant Engineers, Subject Matter Experts, Quality Compliance Experts and others to drive constant improvements • Learn how to do and apply data analysis on machine and network level, for example PI Historian, MES, SCADA • Run Root cause analysis of engineering related machine problems with the goal to minimize unplanned stoppages of our vials- and syringe-devices packaging lines • Identify, evaluate and rate quality relevant parameters of existing setting lists and periodically present results within the Steriles Packaging department #LI-Onsite Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements What you’ll bring to the role: • Looking for an Internship either just before your studies, during your studies or after recently graduated as Master or Bachelor in Engineering, Technics/Mechanics or IT (graduation not longer than ca. 12 months ago) • Good English and intermediate German needed, good communication skills • Enthusiasm for Packaging topics in the Pharmaceutical Industry and GMP • Ability to assess and to evaluate quality requirements and bring it into technical context • Problem-solving oriented and working skillfully • Good organizational and planning skills • Soft skills: self-driven, motivated, willing to learn, strong team spirit • Experience within Pharmaceutical Industry and basic understanding of GMP would be an advantage 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 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 357950BR Dec 02, 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. Unser Werk Novartis Stein Steriles ist einer der wichtigsten Standorte für innovative, hochqualitative, sterile Medikamente, die wir jeden Tag für unsere Patienten in über 150 Ländern produzieren und verpacken. Um die Abteilung Novartis Technical Operations zu verstärken, suchen wir per sofort 1 Prozessmitarbeiter(-in) im Bereich der Flüssigvialabfüllung (Isolatortechnologie) mit Schichtbereitschaft (inkl. Nachtschicht). Zu Ihren Aufgaben gehören unter anderem: • Abfüllung der hergestellten Produktlösung in der korrekten Menge und unter Einhaltung aseptischer Bedingungen • Bedienung der Vial/Flaschen 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 Durchführen 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 Was Sie mitbringen werden: • Einige Jahre Berufserfahrung in der Biotechproduktion von Vorteil • Erfahrung in der Bedienung von Anlagen (e.g. CIP/SIP, Isolator und FVA - Füllverschliessanlage) • Abgeschlossene Berufslehre als Chemie- und Pharmatechnologe oder ähnliches oder langjährige, einschlägige Berufserfahrung in der Chemie- oder Pharmabranche • Technisches Verständnis, Erfahrung in GMP Umgebung, zügiges und eigenständiges erlangen von Kenntnissen über die relevanten SOP's und Vorschriften (z.B. Anlage-spezifische SOP's, Ansatzspezifische SOPs, Hygienekonzept, GSU-Vorschriften, etc.). • Sehr gute Deutschkenntnisse in Wort und Schrift. Englischkenntnisse sind gewünscht. • Motivation, Flexibilität und Team Fähigkeit • Affinität für digitale Technologien (MES/PAS-X Erfahrung) • SAP Erfahrung von Vorteil • Train-The-Trainer Ausbildung von Vorteil Warum Novartis? 799 Millionen! - so viele Menschen haben wir mit unseren Produkten erreicht. Und obwohl wir darauf stolz sind, stellen wir uns kontinuierlich die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Menschenleben verbessern und verlängern? Wir sind überzeugt, dass wir Antworten finden können, wenn neugierige, couragierte und teamorientierte Menschen bestärkt werden, den Status Quo zu hinterfragen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden gegebenenfalls im Vorstellungsgespräch besprochen. Werden Sie Mitglied in unserem Novartis Netzwerk: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit LARGE MOLECULES Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work Yes 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 358235BR Dec 01, 2022 Switzerland Job Description 365 Tage im Jahr arbeitet unser globales Produktions- und Liefernetzwerk, um sicherzustellen, dass unsere Patienten die Behandlungen erhalten, die sie für ein längeres und gesünderes Leben benötigen. Der Prozessmitarbeiter ist verantwortlich für die Überwachung der ihm zugeteilten Anlagen. Er übernimmt die fachliche Weisungsbefugnis in Auftrag des Team Leaders. Der Mitarbeiter kann sowohl an Verpackungsanlagen als auch an Etikettierungsanlagen eingesetzt werden. Dabei hat er vollumfängliche Kenntnisse über die relevanten SOP's und Vorschriften (z.B. anlagespezifische SOP's, Hygienekonzept, GSU-Vorschriften, etc.). Ihr Verantwortungsbereich: •Verantwortlich für die Überwachung der Anlage in seinem Bereich und für die konsequente Einhaltung der SOP`s, Daten Integrität, Hygiene und Sicherheitsvorschriften • Sorgt für Sauberkeit, Hygiene und Ordnung im zu verantwortenden Bereich •Umsetzen der 5S Standards •Durchführung der Startkontrolle (erste Kontrolle) und IPC sowie der Endkontrolle (Alter Auftrag, Bruch zählen) •Selbstständige, vollständige und fehlerfreie Eintragungen in Herstelldokumente, Log-Bücher und Dateneingabe •Anlernen/ Weiterbilden der Mitarbeitenden -> TrainerZertifizierung/ Train the Trainer •Problemlösungen bei Unterbruch •Personal einteilen und Prozesse Team - und Produktübergreifend sehen und mitplanen. -> Vertretung Teamleader in Abwesenheit (on the job) •HSE Monatsthemen mit Mitarbeitern in der Produktion behandeln Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie für die Position mitbringen: Ausbildung: • abgeschlossene Berufslehre als Chemie- Pharmatechnologe oder vergleichbares • oder Reinraumqualifizierung • oder langjährige, einschlägige Berufserfahrung in der Chemie- oder Pharmabranche und Novartis IHK-Kurs Sprachen: • Gute, fliessende Deutschkenntnisse • Englisch (Grundkenntnisse) Erfahrung: • Vollumfängliche Kenntnisse über die relevanten SOP's und Vorschriften (z.B. anlagespezifische SOP's, Hygienekonzept, GSU-Vorschriften, etc.) • Kenntnisse in unten aufgeführten Kentnissen 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 LARGE MOLECULES 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 357945BR Dec 01, 2022 Switzerland Job Description 365 Tage im Jahr arbeitet unser globales Produktions- und Liefernetzwerk, um sicherzustellen, dass unsere Patienten die Behandlungen erhalten, die sie für ein längeres und gesünderes Leben benötigen. Der Prozessmitarbeiter ist verantwortlich für die Überwachung der ihm zugeteilten Anlagen. Er übernimmt die fachliche Weisungsbefugnis in Auftrag des Team Leaders. Der Mitarbeiter kann sowohl an Verpackungsanlagen als auch an Etikettierungsanlagen eingesetzt werden. Dabei hat er vollumfängliche Kenntnisse über die relevanten SOP's und Vorschriften (z.B. anlagespezifische SOP's, Hygienekonzept, GSU-Vorschriften, etc.). Ihr Verantwortungsbereich: •Verantwortlich für die Überwachung der Anlage in seinem Bereich und für die konsequente Einhaltung der SOP`s, Daten Integrität, Hygiene und Sicherheitsvorschriften • Sorgt für Sauberkeit, Hygiene und Ordnung im zu verantwortenden Bereich •Umsetzen der 5S Standards •Durchführung der Startkontrolle (erste Kontrolle) und IPC sowie der Endkontrolle (Alter Auftrag, Bruch zählen) •Selbstständige, vollständige und fehlerfreie Eintragungen in Herstelldokumente, Log-Bücher und Dateneingabe •Anlernen/ Weiterbilden der Mitarbeitenden -> TrainerZertifizierung/ Train the Trainer •Problemlösungen bei Unterbruch •Personal einteilen und Prozesse Team - und Produktübergreifend sehen und mitplanen. -> Vertretung Teamleader in Abwesenheit (on the job) •HSE Monatsthemen mit Mitarbeitern in der Produktion behandeln Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie für die Position mitbringen: Ausbildung: • abgeschlossene Berufslehre als Chemie- Pharmatechnologe oder vergleichbares • oder Reinraumqualifizierung • oder langjährige, einschlägige Berufserfahrung in der Chemie- oder Pharmabranche und Novartis IHK-Kurs Sprachen: • Gute, fliessende Deutschkenntnisse • Englisch (Grundkenntnisse) Erfahrung: • Vollumfängliche Kenntnisse über die relevanten SOP's und Vorschriften (z.B. anlagespezifische SOP's, Hygienekonzept, GSU-Vorschriften, etc.) • Kenntnisse in unten aufgeführten Kentnissen 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 LARGE MOLECULES 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 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 353008BR Oct 13, 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 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 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 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 357757BR Nov 25, 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. Your key responsibilities: Your responsibilities include, but are not limited to: - Ensuring compliance with legal and internal Health, Safety and Environmental regulations and keeping up high Safety standards to prevent incidents - performs and supports risk assessments and promotes Safety Culture across Laboratories and Cell & Gene Technology Production at Campus Stein - acts as SPOC - technical support for Rhein Valley sites (laboratory safety) - Ensuring the information flow on Site with the management and with all other internal and external parties incl. Authorities - Supports Audits, Projects, Reporting and other HSE tasks. 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 - Preferably completed Studies Chemical/Pharmaceutical or Safety Engineering (Technical School) with completed Safety Education (ASGS Specialist / Sicherheitsfachmann-Frau, Sicherheitsingenieur-In EKAS Richtlinie 6508) - Fluent in German, good in English - At least 2 years of professional experience in occupational safety and accident prevention 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!Division Novartis Technical Operations Business Unit SITE DEVELOPMENT Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Facilities & Administration Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 354722BR Nov 25, 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. The Account Manager represents the interface to all site development customers including non-Novartis site users and is responsible for contract management with these site customers, be their first point of contact, creates and offers new service solutions and manages the customer relationships with the aim of increasing customer satisfaction and the utilization of services and thus optimizing costs and benefits. Your responsibilities include, but are not limited to: • Manage the implementation of agreements with the customer and the fulfillment of mutual financial and contractual obligations • Management of involvement from other departments to assure flawless contract execution as well as service portfolio development and optimizations • Support acquisition of new tenants to all Rhine Valley sites in cooperation with the Business Development Managers and global supporting teams • SPOC for all site customers (Novartis and 3rd parties) at the Site Development Rhine Valley sites and support of communication of relevant information to the customer organization • Lead the creation, adjustment or extension of Lease contracts, Site Service Agreements and specific SLA’s for new and existing tenant contracts in cooperation with the appropriate departments, including finance, legal administration and technical departments • Search, identify and specify customer needs and selling of services based on appropriate pricing structures within existing framework agreements or separate service contracts • Independent implementation of periodical customer satisfaction queries, reporting of service KPI evaluations and translation into execution of measures that lead to an increase in customer satisfaction • Independently manage inquiries, queries or complaints from the site customers (Novartis and 3rd parties) together with the specialist departments of the Site Development Organization • Creation, optimization and maintenance of the service catalogue for all offered services incl. prices and delivery/contractual requirements (e.g. KPIs) • Stakeholder management across internal and external platforms to successfully manage and strengthen the relationships as a service provider to internal and external customers • Actively promote the site development to potential future customers and various external parties operating in the Life-Science field 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 required as a minimum, Master’s degree preferred • Fluent in German and English, knowledge of additional languages is an advantage • >5 years of sales and customer relationship management experience in a market with long-term relationships • Minimum 4+ years in the healthcare industry or equivalent • Extensive experience in category, demand management, business partnering and negotiations • Experience in leading and developing cross-functional teams within a matrix organization and across geographies and cultures • Knowledge of real-estate and site supporting services 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! 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 Novartis Technical Operations Business Unit SITE DEVELOPMENT Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

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

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

Job ID 352755BR Oct 13, 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: Nov/Dec, 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 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 352092BR Oct 12, 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 We expect new positions to come up for a start in January 2023. Please submit a cover letter that includes your motivation and from when you will be available. Thank you. 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 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 353047BR Oct 07, 2022 Switzerland Job Description Equipment Specialist (*80-100%), Stein, Switzerland 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 Equipment Specialist 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! Ihr Verantwortungsbereich: • Teilnahme an den Herstellungsprozessen • Übernahme sämtlicher Aufgaben/Verantwortungen des Gerätebedieners • 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 Diese Position wird auf 2 Jahre befristet Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Minimum Requirements Was Sie für die Position mitbringen: • 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 Desinfektion der Produktionsanlagen und -räume • Verantwortung für die Haushaltsführung des Produktionsbereichs (Reinigung, Ordnung, 5S, etc.) • Einhaltung und Durchsetzen der Gesundheits-, Sicherheits- und Umweltregeln und -richtlinien (HSE) • Anwendung und Durchsetzen der aktuellen GMP-Regeln • Ausführung sämtlich zugewiesener Tätigkeiten gemäß den GMP-, Arbeitsschutz- und Umweltrichtlinien • Fliessende Kommunikation in Deutsch Warum Novartis? Über 799 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir sind davon überzeugt, dass wir Antworten finden können, wenn neugierige, mutige und teamorientierte Menschen dazu ermutigt werden, den Status quo in Frage zu stellen, mutige Entscheidungen zu treffen und innovative Wege zu gehen. *Einige Einschränkungen für flexible Arbeitsmöglichkeiten können gelten und werden gegebenenfalls im Vorstellungsgespräch besprochen. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/networkDivision Novartis Technical Operations Business Unit 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 358054BR Nov 22, 2022 Switzerland Job Description 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. 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. 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 What you’ll bring to the role: • University degree in Science, Pharmacy or Chemical Engineering, Pharmaceutical Technology or equivalent • 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!Division Novartis Technical Operations Business Unit LARGE MOLECULES Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work No 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 357871BR Nov 11, 2022 USA Job Description 1,800+ associates. 86 countries. One Regulatory Affairs. At Novartis your voice, experience, and quality mindset can truly make a difference in Regulatory Affairs (RA). Novartis has a unique and promising portfolio with 70 projects as potential NMEs in development, 65 projects in Phase 3 or already undergoing registration, and 100 Phase 1/2 projects. We also focus on rare disease areas; in fact, more than 80% of our innovation is targeted on areas of high unmet need. In many cases, we can offer family friendly work flexibility to facilitate your physical and mental health. Read on to learn about the role available in Regulatory Affairs. We hope you will consider joining our global OneRA family. The RA Senior Global Labeling Manager (Sr. GLM) is responsible for the creation and maintenance of regulatory compliant, competitive, and up-to-date core labeling documents for assigned developmental programs and Novartis Innovative Medicines products. The assigned products should be of higher complexity products and may include developmental programs. The RA Sr. GLM provides strategic and operational regulatory labeling input and works in close collaboration with Expert Labeling Task Force (ELTF) members in creating or maintaining core labeling documents and handling HA or CO labeling queries for assigned products. Your responsibilities will include but are not limited to: • Serve as the labeling lead for all labeling related topics for Novartis products and development projects • Coordinate and lead the ELTF to discuss labeling strategy and reach consensus on labeling course of action and labeling text as appropriate • Lead and/contribute to presentations on labeling related topics for the assigned products at relevant board/forum/committee (e.g., GLC, SMT, MSRB, PSB) • Contribute to global labeling management and continuous improvement initiatives, review and comment on emerging regulatory labeling guidelines • Represent GL during audits and inspections Diversity & Inclusion / EEO The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Minimum Requirements What you’ll bring to the role: • Science based degree, advanced degree preferred (MD, PhD PharmD) • Extensive experience (at least 4-6 years) in global labeling, alternatively extensive experience (5 + years) in related areas of the pharmaceutical industry or Health Authorities • Experience with new product development and with managing Oncology products • US and EU Labeling filing experience • Strong interpersonal, project management, communication, negotiation and problem-solving skills • Ability to lead cross-functional teams in a matrix environment • Sound understanding of medical and scientific terminologies and good understanding of drug safety information 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to: [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. The pay range for this position at commencement of employment is expected to be between $124,000 and $186,000/year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including a sign-on bonus, restricted stock units, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Global Drug Development Business Unit REG AFFAIRS GDD Location USA Site East Hanover, NJ Company / Legal Entity Novartis Pharmaceuticals Alternative Location 1 Switzerland Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 356400BR Oct 28, 2022 USA Job Description One person dies every 37 seconds from Cardiovascular Disease in the United States. At Novartis, we are committed to reducing the global burden of cardiovascular, renal and metabolic diseases on patients, families and their communities. We are focused on developing solutions targeting heart failure (acute and chronic), atherosclerosis, metabolic and renal diseases with the aim of improving quality of life for patients all over the world. The Clinical Development Medical Director (CDMD) is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As CDMD, you will have oversight of the clinical development for the assigned programs and drive execution of the clinical development plan. In addition, you will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. Your responsibilities will include, but are not limited to: • Providing clinical leadership and strategic medical input for all clinical deliverables in the assigned project or section of a clinical program • Leading development of clinical sections of trial and program level regulatory documents • Driving execution the assigned clinical program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable • Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues • Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas • As a medical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards • May work with NIBR (Novartis Institute of Biomedical Research/ Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed. Diversity & Inclusion / EEO The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Minimum Requirements What you'll bring to the role: • MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area; Clinical practice experience 4 years (including residency) and board certification preferred • Minimum of 7 years of experience in clinical research or drug development • Experience in an academic clinical research or industry environment spanning clinical activities in Phases I through IV required • 2 years of contribution to and accomplishment in all aspects of conducting clinical trials (e.g., planning, executing, reporting and publishing) in a global/matrix environment in pharmaceutical industry required. • Working knowledge of disease area is required, with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) and proven ability to understand and interpret basic and clinical scientific research reports • Demonstrated ability to establish effective scientific partnerships with key stakeholders • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes • Previous global people management experience is preferred, though this may include management in a matrix environment Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Accessibility and Reasonable Accommodations: Individuals in need of a reasonable accommodation due to a medical condition or disability for any part of the application process, or to perform the essential functions of a position, please send an e-mail to [email protected] or call +1 (877)395-2339 and let us know the nature of your request and your contact information. Please include the job requisition number in your message. COVID-19: 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/networkDivision Global Drug Development Business Unit CARDIO-RENAL-METAB GDD Location USA Site East Hanover, NJ Company / Legal Entity Novartis Pharmaceuticals Alternative Location 1 Switzerland Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 344724BR Oct 28, 2022 USA Job Description 10! That’s how many pipeline projects Immunology has in Phase 3 or registration and over 25 projects in Phase 1/2. Our Immunology Unit has a pipeline with depth and breadth and is known to be a talent powerhouse. We are uniquely positioned to have a critical impact on bringing innovative medicines to patients across multiple disease areas. This includes developing Novartis’ multi-blockbuster Cosentyx and several novel agents, with an extensive immuno-dermatologic footprint. As Global Program Head, you will have a critical impact of delivering innovation, which drives the Novartis enterprise. You will lead Novartis program(s) through the end-to-end development cycle to seek successful registration and market access. You will drive optimal life cycle management of approved assets, and have overall accountability for quality, time, cost, proactive risk management, and compliance. Furthermore, you will work closely with The Novartis Institutes for BioMedical Research (NIBR) to develop overall disease area strategies and advise the research and early development efforts. You will drive global development, worldwide regulatory approvals, market access and optimized commercial value of the program and are accountable for timelines and budget Your responsibilities will include: • Lead a multidisciplinary team of functional experts focused on securing global regulatory approval, market access and optimized commercial value of the program while ensuring this is achieved with a high quality, full compliance (internal and external, e.g. regulatory, requirements) within budget and in a competitive and timely manner, utilizing both the internal or other identified expert resources necessary for success • Establish short and long range project vision and strategy • Ensure alignment/close collaboration cross global functions, regions and CPOs in regards to strategy and direction • Leverage knowledge, experience, understanding of external stakeholders, internal team capabilities and portfolio needs to develop a compelling, innovative vision and strategy for the program • Establish program strategy and execute implementation through milestones and decision points by leveraging cross-functional teams • Presentation and alignment of project strategy • Communicates clear strategy to program team and functions and ensures that it is reflected in the operation • Ensures rigorous adherence to quality and compliance • Drive talent acquisition among team members and within their sub-teams including active selection and de-selection and performance management of the core membership of the program team • Actively coach and partners with direct reports to build and implement individual development plans and conduct their performance appraisal discussions in close partnership with the line-function heads Diversity & Inclusion / EEO The Novartis Group of Companies are Equal Opportunity Employers and take pride in maintaining a diverse environment. We do not discriminate in recruitment, hiring, training, promotion or other employment practices for reasons of race, color, religion, gender, national origin, age, sexual orientation, gender identity or expression, marital or veteran status, disability, or any other legally protected status. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Minimum Requirements What you’ll bring to the role: • MD or PhD degree in the related discipline • Minimum of 5 years of drug development experience, including experience in Global Program Teams and with dossier submission for new or supplemental indication • Deep drug development experience in immune mediated and/or dermatology diseases. • Prior exposure to and strong awareness of regulatory / market access / commercialization requirements. • Leadership of multidisciplinary teams • Innovative strategic attitude **Some restrictions to flexible working models may apply and will be discussed at 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 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 IHD DU 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