Novartis AG

Job ID 386932BR Dec 01, 2023 Switzerland About the Role 5000+! That’s the number of associates in Biomedical Research at Novartis. This division is the innovation engine of Novartis, focusing on powerful new approaches that will help produce therapeutic breakthroughs for patients. The Discovery Sciences department (DSc) at NIBR drives drug discovery and champions innovative approaches such as Radioligand Therapeutics (RLT). The Chemical Genetics group in DSc, Basel/Switzerland, is seeking a highly motivated, curious, and innovative scientist who is interested in making an impact on drug discovery through scientific technologies and by boosting our endeavors in the identification, characterization, and development of novel RTLs and emerging therapeutic modalities. We are a highly collaborative, global group of researchers exploring the interface of chemistry and biology for projects in early drug discovery. More specifically, we apply and develop encoded library technologies for the discovery of low molecular weight and peptide binders to disease relevant targets and explore emerging drug modalities as novel innovative path to therapeutics. Our group is part of the larger DSc department that encompasses a spectrum of sophisticated capabilities for successful, state-of-the-art drug discovery. Location: Basel, Switzerland #LI-Hybrid Your responsibilities: Your responsibilities include, but are not limited to: • Design, execute, and analyze encoded peptide library screening campaigns for drug discovery projects with an emphasis on Radioligand therapy (RLT) projects • Innovate and further develop existing encoded library technologies and explore novel screening approaches • Contribute experimentally and intellectually to early drug discovery projects and the exploration of novel drug modalities by working in multidisciplinary and collaborative global teams • Prepare and communicate results at internal and external meetings, and in scientific publications. • Mentor and develop junior colleagues in the laboratory. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements • The candidate holds a PhD, or alternatively an MSc with 5+ years of experience in industry, with a background in one or more of the following areas: chemical biology, biochemistry/biophysics, molecular biology, synthetic biology, assay development. • Strong interest in exploring novel screening technologies and therapeutic approaches for drug discovery. • Curiosity, scientific agility, and interdisciplinary mindset (chemistry, biology, technology). • Interest in working in matrixed and collaborative teams. Excellent interpersonal skills. • Ability to adapt to scientific challenges and to generate innovative ideas/solutions. • Excellent communication and presentation skills in oral and written English. Desirable Requirements: • Practical knowledge with encoded library screening: e.g. mRNA- or phage-display, DNA-encoded libraries • Expertise in identifying and characterizing LMW ligands and exploring novel screening technologies at the interface of chemistry and biology • Experience with identifying and developing ligands in the context of RLTs and vectorized therapeutics • Experience with developing and applying tools for analyzing large, complex data sets Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 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/networkDivision Biomedical Research Business Unit DSc 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 383528BR Dec 01, 2023 Switzerland About the Role The purpose of this role is to support the HSE team in the laboratory environment on Basel Site. Key responsibilities: - Provide advice to R&D community on HSE issues and actively supports them for example, on HSE walkthroughs, or meetings. Acts as a contact person for health, safety and environmental questions in the laboratory area and supports the line functions in these topics. Assess working methods, equipment, and processes from an HSE perspective. Assist in the introduction of accident prevention programs and measures, conducts campaigns for the prevention of accidents at work and non-accidents at work. Review incidents and supports investigations (root cause analysis) and the implementation of corrective and preventive actions. Assist the introduction of corrective and preventive measures for the continuous improvement of safety technology and safety standards. Support projects as needed in occupational health & safety. Help in the creation of various trainings and campaigns. Make an active contribution to the safety culture at the site. Key Performance Indicators Support engagement programs Fulfilment of personal and Operations objectives Safety targets and performance goals are achieved. EEO Statement: 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. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Education: Successfully completed apprenticeship as a laboratory technician ASGS Specialist - Occupational Safety Training or willingness to complete it Additional training in the field of biosafety or chemical safety or the willingness to complete it Languages: German, English, any other language is a plus. Experience: Several years of professional experience in the laboratory (preferably in a global pharmaceutical company) Experience in emergency services is an advantage. Organizational skills Communication and motivation skills Diplomatic setting and negotiation skills Can deal with conflicts. 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.Division Operations Business Unit HSE & ES Location Switzerland Site Basel 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 387034BR Dec 01, 2023 Switzerland About the Role 5000+! That’s the number of associates in Biomedical Research at Novartis. This division is the innovation engine of Novartis, focusing on powerful new approaches that will help produce therapeutic breakthroughs for patients. The Discovery Sciences department (DSc) at NIBR drives drug discovery and champions innovative approaches such as Radioligand Therapeutics (RLT). The Protein Sciences group is part of Discovery Sciences. We are a highly collaborative group of scientists that produce and study proteins using biophysics and 3D structures to enable target-based approaches including hit identification and validation. We are currently recruiting a Senior Scientist / Principal Scientist with a strong background and track record in protein expression and purification, in particular membrane proteins. The candidate will join our labs in Basel/Switzerland to work on various drug discovery projects in the RLT space and beyond. This is an excellent opportunity to join a vibrant research community at BR in Basel, Switzerland. The successful candidate will be a curious and highly motivated protein scientist with a collaborative team spirit, excellent organizational and communication skills. Location: Basel, Switzerland #LI-Hybrid Your responsibilities: Your responsibilities include, but are not limited to: • Contribute experimentally and intellectually to early drug discovery projects within multidisciplinary teams • Produce proteins for hit generation and hit validation activities as well as biophysics and structural biology studies • Innovate and further develop existing experimental procedures and implement novel technologies • Work closely with lab associates in a matrix setting, including the mentoring and development of junior team members • Present and communicate results at internal and external meetings and in scientific publications Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements • PhD degree in biochemistry, life sciences, molecular biology or related field, or equivalent relevant research experience in an academic setting and/or in the pharmaceutical/biotech sector • Demonstrated experience with expression, purification, and modification of a range of protein targets; experience with mammalian and insect cell expression systems is a strict requirement, experience with membrane proteins will be considered a strong asset • Proficiency in construct design and tagging strategy using pioneering tools • Mentoring and training skills to develop team members • Analytical skills and an eye for detail to ensure accurate record keeping of high quality data • Excellent communication and presentation skills in oral and written English. • Strong team spirit and a collaborative approach Desirable Requirements: • Prior experience with purification optimization for protein-based assays (eg screening, biophysics or structural biology), including detergent optimization screening • Experience with characterizing protein ligand interactions • Curiosity to explore novel methods and innovative technologies • Experience with protein tracking databases and or workflow tools Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 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/networkDivision Biomedical Research Business Unit DSc 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 359650BR Sep 14, 2023 Switzerland About the Role 90%! Is the percentage of our treatments in development with the potential to be first in class or first in a specific indication! Novartis is deeply committed to transforming the lives of people living with solid tumors. We believe that anyone living with these conditions has the right to a life free from pain, free from symptoms and free from disease - this is our vision for the future. Our mission is to reimagine medicine to extend and improve peoples lives – and our overall company strategy to achieve this is to Focus Novartis as a leading medicine company powered by data science and advanced therapy platforms such as Radioligand Therapy (RLT). Novartis has become the industry leader in RLT after the acquisition of Advanced Accelerator Applications (AAA) and Endocyte in 2018, together with other significant investments to advance radioligand research. Novartis Oncology is now developing a wide range of targeted RLTs, and precision Radioligand Imaging (RLI) agents, for oncology with a rich pipeline targeting multiple tumor types through a phenotypic precision medicine approach. Nuclear Medicine (NM) expertise is key for Novartis Oncology to expand RLT and supportive RLI agents in a sustainable manner. The Clinical Development Medical Director (CDMD) is responsible for leading the planning and management of the assigned RLI clinical program(s) to support the RTL trials from an end-to-end clinical development perspective. As CDMD, you will have oversight of assigned programs and drive execution of the plan. In addition, you will enable an empowered organization, which can navigate in a matrix environment and adjust quickly to business needs. Your responsibilities as a Nuclear Medicine expert will include: • Providing clinical leadership and strategic medical input for all clinical results in the assigned project or section of a clinical program • Leading development of RLI related clinical sections of trial and program level regulatory documents • Driving execution of the program and/or clinical trial in partnership with global line functions, assigned Global Trial Directors (GTDs), and regional/country medical associates, where applicable • Supporting (Senior) Global Program Clinical Head (GPCH) in ensuring overall safety of the molecule for the assigned section, and may act as a core member of the Safety Management Team (SMT), supporting overall program safety reporting in collaboration with Patient Safety colleagues • Supporting the Clinical Development Head (CDH) by providing medical input into Clinical Development Plan (CDP), Integrated Development Plan (IDP) and Clinical Trial Protocol (CTP) reviews, and contributing to/driving development of disease clinical standards for new disease areas • As a Nuclear Medicine physician specialist, supporting the (Sr.) GPCH or CDH in interactions with external and internal partners and decision boards • Contribute to the publication strategy of RLI/RLT compounds from the scientific standpoint • May work with NIBR (Novartis Institute of Biomedical Research)/ Translational Medical Sciences) to drive transition of pre-PoC (Proof of Concept) projects to DDP (Development Decision Point) and with BD&L (Business Development & Licensing) including target identification and due diligences together with other medical matters, as needed. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you'll bring to the role: • Nuclear medicine Physician/Medical Doctor (EU or US Board certified) • Sophisticated knowledge and clinical training in oncology PET; Clinical practice experience ≥ 5 years preferred. • Experience in Clinical Trials with a PET component • Experience with Radioligand therapy • A consistent track record to interpret, discuss and present data relating to clinical trial(s) with a Nuclear Medicine component • Demonstrated ability to establish effective scientific partnerships with key partners • Solid understanding of GCP, clinical trial design, statistics, regulatory and clinical development processes • Some restrictions to flexible working models may apply and will be discussed at interview if applicable Why consider Novartis? 769 million lives were touched by Novartis medicines in 2020, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/networkDivision Development Business Unit OHD GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 387868BR Dec 01, 2023 Switzerland About the Role We are looking for a highly motivated recent PhD in Chemical and Analytical Development (CHAD) enrolled in our dynamic Early Talent Program (ETP) to support and expand the development of mixed modalities across the organization. This program is designed to offer young talents unique insights into various areas of drug development. This year we provide the opportunity to work at the interface of biology and chemistry. Rotations within CHAD Basel from synthetic labs supporting route and process development of mixed modalities to the manufacturing pilot plant, with a strong focus on the downstream processing of oligonucleotides, will provide a comprehensive overview on how a research idea is developing to a market-ready drug. During these rotations, you will be exposed to current standards in safety, quality, 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. Preferred start date / March 2024 Latest start date / April 2024 Duration: 24 month Key responsibilities: We are looking for a highly motivated recent chemical or process engineering PhD to support and expand the development of mixed modalities across the organization. Your responsibilities will vary throughout the program stages and include: • Drive scientific innovations, processes or products • Develop and scale-up cutting-edge processes for the downstream purification of mixed modalities such as oligonucleotides and peptides. • Plan and execute lab experiments • Support scale-up activities, manage and supervise internal and external pilot plant campaigns, write regulatory relevant documents and interact with Quality Assurance (QA) • Support standard synthetic and analytical development activities on portfolio relevant projects • Communicate the results including thorough interpretation efficiently • Become part of an interdisciplinary Team of Analysts, Chemists and Chemical Engineers #LI-Onsite Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Essential requirements: Scientific background: • Preferentially, a completed PhD in chemical engineering or other relevant subjects in the field of engineering • A sound background on typical purification unit operations such as chromatography, ultrafiltration, lyophilization, distillation and/or extraction. • Basic theoretical and practical synthetic and analytical chemistry skills • An excellent track record of original research Soft Skills: • Ready to work in international and multidisciplinary teams • Open minded personality and “can do” attitude • Strong interpersonal and communication skills are required • Fluency in English Desirable requirements: • Previous exposure to larger molecules such as peptides, proteins or oligonucleotides are an advantage • German proficiency is a plus Please submit a cover letter that includes your motivation for the position and from when you will be available. Thank you. Why Novartis?Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mis-sion and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity and Inclusion / EEO: (Use provided wording - do not change) Novartis is committed to building an outstanding, inclusive work environment and diverse teams repre-sentative of the patients and communities we serve. Accessibility and accommodation: (Use provided wording - do not change) Novartis is committed to working with and providing reasonable accommodation to all individuals. If, be-cause of a medical condition or disability, you need a reasonable accommodation for any part of the re-cruitment process, or in order to receive more detailed information about the essential functions of a po-sition, 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: (Use provided wording - do not change) 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 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 387871BR Dec 01, 2023 Switzerland About the Role We are looking for a highly motivated recent PhD in Chemical and Analytical Development (CHAD) enrolled in our dynamic Early Talent Program (ETP) to support and expand the development of mixed modalities across the organization. This program is designed to offer young talents unique insights into various areas of drug development. This year we provide the opportunity to collect first experience of applied analytical sciences in the pharmaceutical industry. Rotations various analytical labs in CHAD/TRD Basel (e.g. analytical labs supporting route and process development, QC labs, in-process labs supporting pilot plant manufacturing, analytical labs Drug substance, characterisation and analysis of new modalities) will provide a comprehensive overview on drug development within Novartis. During these rotations, you will be exposed to current standards in safety, quality, 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. Preferred start date / March 2024 Latest start date / April 2024 Duration: 24 months Key responsibilities: • Evaluate and implement state-of-the-art analytical technology to support innovation as well as processes and products quality improvement • Design, plan, perform, interpret, report and communicate results of analytical experiments related to the API (small molecules, conjugates, peptides, oligonucleotides) control strategy • Support analytical development activities on innovative projects. • Support analytical transfer activities, write regulatory relevant document and interact with Quality Assurance • Participate in scientific exchange groups within Novartis and external world as well as maintain excellent collaborations with our customers. #LI-Onsite Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Essential requirements: • A completed PhD in analytical chemistry or related discipline. • Fluency in English • Strong analytical, chemical and/or engineering knowledge required • An excellent track record of original research and extensive experience of analytical sciences using “state of the art” technologies (e.g. HRMS, separation sciences, NMR, and/or lab automation tools etc...). • Advanced knowledge in analytical method development or characterisation analysis (e.g. non-targeted or targeted screening etc...). • Good knowledge of software and computer tools (e.g. MS Office), and relevant analytical software (e.g. Chromatography and MS software, MS data processing, deconvolution). • Ready to expand own knowledge, open minded with an international outlook. • Finally, since all work takes place in multidisciplinary project teams, track record on strong interpersonal and communication skills are required. Desirable requirements: • additional German proficiency is a plus • additional knowledge in pharmaceutical/ biopharmaceutical/ sciences is an asset. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. 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/networkDivision 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 386933BR Dec 01, 2023 Switzerland About the Role 5000+! That’s the number of associates in Biomedical Research at Novartis. This division is the innovation engine of Novartis, focusing on powerful new approaches that will help produce therapeutic breakthroughs for patients. The Discovery Sciences department (DSc) at NIBR drives drug discovery and champions innovative approaches such as Radioligand Therapeutics (RLT). The Chemical Genetics group in DSc, Basel/Switzerland, is seeking a highly motivated, curious, and innovative scientist who is interested in making an impact on drug discovery through scientific technologies and by boosting our endeavors in the identification, characterization, and development of novel RTLs and emerging therapeutic modalities. We are a highly collaborative, global group of researchers exploring the interface of chemistry and biology for projects in early drug discovery. More specifically, we apply and develop encoded library technologies for the discovery of low molecular weight and peptide binders to disease relevant targets and explore emerging drug modalities as novel innovative path to therapeutics. Our group is part of the larger DSc department that encompasses a spectrum of sophisticated capabilities for successful, state-of-the-art drug discovery. Location: Basel, Switzerland #LI-Hybrid Your responsibilities: Your responsibilities include, but are not limited to: • Design and analyze encoded chemical library screening campaigns for drug discovery projects with an emphasis on Radioligand Therapeutic (RLT) projects • Define DNA Encoded Chemical Libraries (DEL) team goals and priorities in collaboration with cross-functional stakeholders • Guide the team to deliver impactful results for current drug discovery projects and to develop innovative approaches to address emerging needs • Innovate and further develop existing encoded library technologies and explore novel screening approaches • Contribute to early drug discovery projects and the exploration of novel drug modalities by working in multidisciplinary and collaborative global teams • Prepare and communicate results at internal and external meetings, and in scientific publications • Mentor direct reports and junior colleagues and provide career development opportunities Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements • The candidate holds a PhD and 5+ years of experience in industry. A strong background in one or more of the following areas in required: chemical biology, biochemistry/biophysics or molecular biology. • Extensive expertise in identifying and characterizing LMW ligands and exploring novel screening technologies as evidenced by publication record • Experience in driving drug discovery projects in multidisciplinary teams. Ability to work efficiently with dynamic and interdisciplinary teams • Strong interest in prototyping novel therapeutic modalities at the interface at chemistry and biology • Excellent communication and presentation skills in oral and written English. Ability to interact effectively across the organization. • Track record in team and project leadership. Experience in managing and developing a team of scientists. Excellent interpersonal skills. • Curiosity, scientific agility, and interdisciplinary mindset (chemistry, biology, technology). • Ability to adapt to scientific challenges and to generate innovative ideas/solutions. Desirable Requirements: • Practical knowledge with encoded library technologies: e.g. DNA-encoded libraries, mRNA- or phage-display • Experience with developing and applying tools for analyzing large, complex data sets • Experience with identifying and developing ligands in the context of RLTs and vectorized therapeutics • Experience working in a global, matrixed organization. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 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/networkDivision Biomedical Research Business Unit DSc 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 386970BR Nov 28, 2023 Switzerland About the Role Global Security Intelligence Unit (GSIU) provides timely and relevant intelligence in order to protect Novartis associates, patients, assets, travelers, brands, reputation and intellectual property. We are looking for an intern to join our intelligence team to collect, analyze and disseminate information to assess threats, capabilities, vulnerabilities and opportunities that may impact Novartis associates and assets. The candidate must have a passion for intelligence, with a strong desire to learn and develop in a security intelligence arena. They must demonstrate strong communication skills and be able to work in a time pressured environment. In addition to the day-to-day tasks, as a GS Intelligence Intern, you will be deployed on projects and have the opportunity to develop experience within various Global Security departments. Preferred start date: January 2024 Duration: 6 months Key responsibilities: • Open-source intelligence research in support of the intelligence analysts • Monitoring of geopolitical updates and providing succinct summaries • Contribute to the research and collection of threat information from multiple sources, based on agreed intelligence requirements, and using this to create timely, clear, accurate and actionable security intelligence, threat assessments, management briefings, security alerts, country risk assessments, source reports, multi-media presentations, workshops, and training. • Responsible for data-entry and maintaining, reviewing and updating databases relating to threat entities and their relationships through events and time. • Provide administrative and project support to the Global Security Leadership Team. #LI-Onsite Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Essential requirements: • Education: Masters graduate in a security, intelligence or criminology or similar field (completed within the past ca. 12 months) • Languages: Business-level English; additional language(s) preferred • Experience/Professional requirements: o You have a good knowledge of English and Microsoft Office (Outlook, Word, PowerPoint and Excel). o Be able to condense complex and voluminous data into concise intelligence products. o In taking on your tasks, you prove yourself as a strong planner and show the necessary flexibility. o In addition, you can work independently, under time pressures, and have a healthy dose of assertiveness. o Strong report writing skills - you can present your findings in a structured, succinct and convincing way. Desirable requirements: • Experience in an intelligence related role • Training in intelligence analysis, open source intelligence research Please submit a cover letter that includes your motivation for the position and from when you will be available. Thank you. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture 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/networkDivision Legal Business Unit S&L 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 386701BR Nov 30, 2023 Switzerland About the Role Materials Science Unit is looking for highly motivated Materials Science Expert to contribute as a subject matter expert (SME) across all development phases to assigned internal and/or external project activities and deliverables that are under the responsibility and/or accountability of PHAD Materials Science unit. You will act as a point of contact for assigned projects, lead all relevant associated activities by handing-on experience with material characterization techniques as well as a problem-solving attitude with the ability to set priorities and address unforeseen stakeholders needs. Specifically, as Materials Science Expert you are asked to develop and perform a variety of routine and complex analytical procedures to characterize and understand complex composite materials in the form of liquids, semisolids and powders by various testing techniques (mainly in the field of viscosity and rheology characterization and understanding of surface chemistry). You will provide an independent scientific project drive to support the timely development and delivery of drug substances (DS) aligned with drug product needs, pharmaceutical intermediates (PI) and drug products (DP). You will be working in interdisciplinary scientific cross-functional teams and strategically you bridge the interface between DS and DP during pre-clinical, clinical, and commercial development, whilst ensuring full business alignment with other line functions and project sub teams. We are offering an opportunity for growth with the expectation that in this role you will acquire experience in leading projects, teams in a matrix environment, both internally and externally. Your key responsibilities will include: • Perform a variety of routine and complex analytical procedures to analyze composite materials in the form of liquids, semisolids and powders by various testing techniques, among them, mainly: rheology e.g. to characterize flow behavior and viscoelastic properties of liquids and semisolids materials, to assess the mechanical and thermal stability. • Manage separation techniques including size exclusion chromatography with multi-angle light scattering (SEC-MALS). • Support physicochemical characterisation of polymers including e.g. cloud point determination, rheological measurements, particle characterization, NMR. Performing wetting, adhesion testing (e.g. contact angle,), optical microscopy and static light scattering analyses (SLS) • Perform routine viscosity tests (e.g. viscosity and flow curves, dynamic viscosity measurements) by various methods (rotational viscometer; falling ball measuring principle, Höppler DIN 53015 and ISO 12058) and at the occurrence support as deputy images acquisition of drug products by optical microscopy • Operate and maintain testing equipment incl. troubleshoot and perform preventive maintenance on equipment (at the occurrence also GxP) and/or coordinate maintenance through equipment vendors. • Develop and document new analytical methods, ensure high quality data and enter them in LIMS system and report the results in clear analytical reports. • Maintain accurate records and documentation such as laboratory experience e.g., following SOPs. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Minimum requirements: • Postgraduate, preferentially with a PhD in physical chemistry, materials science, chemical engineering, or related disciplines. • Ideally with minimum 3 years of successful pharmaceutical industry experience as a subject matter expert. • Strong expertise in physicochemical polymers characterization and in rheology • Sound knowledge of data generation and processing • Problem solving mindset: anticipating issues and proactively finding solutions independently. • Experience in working and managing complex stakeholder environments across line functions. • Excellent planning and work prioritization skills. • Interdisciplinary thinking and strength in cross-functional collaboration. • English (fluent) required. German desirable. • Good communication, presentation, technical writing skills. • Familiarity with GMP requirements would be advantageous. 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.Division Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 383704BR Nov 01, 2023 Switzerland About the Role Location: Onsite in Basel, Switzerland. #onsite Novartis’ Comparative Medicine (CM) labs and teams is a key partner with Novartis Biomedical Research 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 Biomedical Research 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 Biomedical Research 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 BioMedical Research. 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 We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you will bring to the role: • You will hold either a minimum qualification of a Doctorate in Veterinary Medicine (DVM), or a Masters or PhD with a minimum 3-5 years experience in in-vivo research • Experienced in delivering in-vivo training programs and/or advanced technical skills in animal research • Accredited or eligible to perform and direct animal experimentation • Leadership/management skills. Proven experience in delivering training and mentoring of in-vivo scientists is beneficial. • 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 Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 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. * Restrictions on flexible working options may apply and will be discussed during interview if applicable.Division Biomedical Research Business Unit Strategy, Portfolio & Operations 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 387140BR Nov 30, 2023 Switzerland About the Role Location: Basel, Switzerland Job Purpose: Novartis holds a rich development portfolio of small molecules ready to develop into innovative patient centric oral dosage forms. As a Formulation Project Leader working on oral dosage forms, you will lead and run all formulation and manufacturing activities linked to pharmaceutical development for oral dosage forms for small molecules (New Chemical Entities; NCE). The focus of that role is to define and develop formulations and processes suitable for initial first-in-human trials until scale-up and transfer to enable commercial manufacturing of our future Drug Products and in particular for “enabling” formulations. Your responsibilities will include but are not limited to: • You are accountable for all formulation and manufacturing process deliverables incl. scientific documentation and excipient qualification for all assigned projects. • You have a passion for innovative formulation and process development approached, including applying modeling and advanced digital skills. • You create, own and update formulation project plans aligned with the control strategy being in line with the overall Drug Product (DP), TRD project plan, and internal guidance. • You drive DP development and supply activities with scientific and technological excellence. You closely collaborate with Drug Product sub-team members. You understand, identify and manage with them together critical aspects around DS, DP, packaging and analytics. • You drive regular exchange with Biopharmaceutics Experts to understand critical factors for absorption and DP-performance and build this understanding into your development strategy. • You ensure authoring of accurate, comprehensible, structured, complete and legible development reports and “Supply documents” to allow timely start of development trials, process transfers and supply activities. • You contribute to the generation of filing dossiers, answer DP related questions in inspections and support Health Authority requests. • You have a passion for innovative formulation and process development approached, including applying modeling advanced digital skills Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you’ll bring to the role: • Advanced degree in relevant scientific field (i.e. minimum PhD) • Minimum 2-4 years of successful industry experience in the development of pharmaceutical formulations in a matrix organization. Focus: Formulation development (small molecules NCE) and scale up of manufacturing processes into oral drug products for commercialization • Desired: Good knowledge of Data science, Data visualization and use of programming language such as Python. Experience with developing formulations for oral delivery of molecules having permeability challenges (including small molecules, peptides, proteins) • Interdisciplinary thinking and curiosity about collaboration with other functions • Broad and profound understanding of formulation and process development activities. • Good knowledge of laboratory and/or technical tools (e.g. QbD, PAT) as well as knowledge of relevant GxP regulations and policies • Successfully demonstrated track record of creativity and problem solving in projects. • Good interpersonal skills, organizational, planning and negotiation skills (German language skills desired). Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 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. Commitment to Diversity and 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 Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 385923BR Nov 01, 2023 Switzerland About the Role 30 million! That is the estimated number of patients worldwide suffering from inflammatory arthritis. Join Novartis to help find the right drugs that transform and improve patients' lives all around the world. You will join an international team of clinicians and scientists making significant impact on autoimmune diseases with high unmet medical need, taking new medicines into early-stage clinical trials: in many cases you will be the first to witness the effectiveness of a new medicine that may transform the lives of millions. Your medical and scientific leadership / expertise will significantly impacts the Novartis autoimmune drug development pipeline. Go to https://www.novartis.com/our-science and scroll to the Autoimmunity research area and Translational Medicine area for more information Your responsibilities will include: • Medical / scientific contributor and leader of complex global cross-functional teams. Our successful drug discovery and development environment has close collaboration across Research, Clinical Research and Development. • Major initiator of the Proof-of-Concept strategy and the early Clinical Development Plan. Develop and implement strategies for efficient, high value management of drug development projects leading to clinical Proof-of-Concept and competitiveness of compounds • Develop and implement disease area and biomarker strategies: contribute effectively to the preclinical and clinical Disease Area strategies, project-specific Biomarker strategy, innovative target identification and in-licensing efforts resulting in a high quality preclinical and clinical portfolio • Ensure full implementation of studies during the Proof-of-Concept phase by providing medical and scientific leadership and expertise to all line functions on the project team, and direct or supervisory medical support for all pharmacokinetic studies • Translational Medicine representative to Health Authorities in matters and meetings that focus on early exploratory development: negotiate effectively with Health Authority representatives on all aspects of Translational Medicine and obtain results favorable to Novartis. Translational Medicine representative to Translational Medicine/medically related experts and organizations, advancing the interests of Novartis by your knowledge, style and personal skill and enhancing the position of Novartis with these individuals and groups • Contribute senior expertise to Research in support of target identification, selection, target validation and preclinical development of compounds. Review and evaluates cross-Disease Area activities at and beyond the early compound optimization stage. Provide clinical context and help design optimal preclinical studies • Evaluate clinical centers and foster communication with crucial collaborating investigators. Interact effectively with external medical and non-medical leaders and be an internal Novartis expert leader in your scientific and clinical subspecialty field. Matrix people responsibility per project: 5-8 cross-functional members from Translational Medicine plus 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 expert in your field, you drive project team clinical strategies and bring global credibility across various Novartis Institutes and Divisions as well as country organizations Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements This position is written for Director - we can hire Associate Director for those with careers that include less established science / clinical study experience. We support International family relocation and integration support to Switzerland. What you’ll bring to the role: • MD and Board certified Rheumatologist (or similar relevant sub-specialty clinical training with directly relevant patient experience) with PhD-level basic science. A completed relevant postdoctoral fellowship is strongly preferred • Advanced / business-level / fluent English (oral and written) • Recognized for your medical expertise: an experienced Clinician treating relevant patient groups at an academic medical center or private medical practice group • Recognized for your scientific expertise: respected by colleagues internally and externally, you’ve made significant contributions to your field and created / established new concepts; you have a record of high quality publications in international scientific journals • Experience designing and conducting early phase clinical trials including for inflammatory arthritis: either from pharma/biotech, a senior CRO role where you were responsible for the medical relationship and studies with Sponsors, or from a relevant academic medical center with co-PI ideally also PI clinical trial experience. 5+ years trial experience particularly in inflammatory arthritis preferred • You are used to working independently and within teams including autoimmune disease research scientists and non-scientists on study planning and execution, demonstrating competence in a broad range of project and more strategic planning skills and leading complex cross-functional/matrix project teams Your behavioural characteristics • Demonstrated passion for treating patients and science • Strategic thinker: you have created major innovations, networked with and influenced external medical leaders with your clear and logical presentation of complex strategic issues • Results-driven self-starter and decision taker • Strong cooperative team player, flexible in a changing environment • Good planning, prioritisation, problem solving and organisational skills • Resilient, energetic and enthusiastic; responding constructively to challenging new ideas and input ABOUT TRANSLATIONAL MEDICINE: Translational Medicine is a global group of scientists and physicians working at the pre-clinical and early clinical stage of drug discovery. Our Physician-Scientists drive innovative and cutting-edge science through the selection, profiling and effective global development of successful medicines, integrating clinical science into the discovery and preclinical development phase. Our Translational Medicine concepts are driven by medical needs of patients and the concept of personalized medicine, tailoring the drug, dose and dosing regimen to the patient so the clinical response is optimal in efficacy and safety. We focus from identification of drug targets (molecular pathways relevant to disease) up to the completion of Proof of Concept (Phase IIa studies). Our Translational Medicine Experts are part of preclinical project teams in all drug discovery phases and help design the pathway for First in Human studies (healthy volunteer) that bridge to studies in the patient population. They have the comprehensive responsibility for designing and executing the early clinical drug development phase with a project team including research, biomarkers, biostatistics, modeling & simulation, toxicology, technical experts and clinical trial teams. 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.Division Biomedical Research 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 386786BR Nov 28, 2023 Switzerland About the Role Novartis provides healthcare solutions that address the evolving needs of patients and societies worldwide. Our broad portfolio includes innovative pharmaceuticals and oncology medicines. Our mission is to discover new ways to improve and extend people’s lives. Our vision is to be a trusted leader in changing the practice of medicine. Our strategy is to use science-based innovation to deliver better outcomes for patients in growing areas of healthcare. Our Innovative Medicines Division is a world leader in offering innovation-driven, patent-protected medicines to patients and physicians. The Innovative Medicines Division conducts research, develops, manufactures, distributes and sells patented pharmaceuticals. Timing: as soon as possible (expected start date: preferably January or February 2024) Duration: 6 months Your responsibilities The Novartis Development and IM Legal Team is looking for university graduates for traineeships in the Global and Swiss legal departments in Basel. The traineeships offer an excellent opportunity to gain practical experience in a large international pharmaceutical corporation. Main responsibilities include: • Support the legal counsels in their daily work on a wide range of legal matters and projects in areas such as contract law, commercial law, licensing, pharmaceutical/healthcare laws, anti-trust law and transactions • Legal research and drafting documents on various legal issues and disputes in private and public law areas • Support a diverse range of development, regulatory, digital and commercial matters relating to the development and commercialization of pharmaceutical products • Assist with the drafting, negotiation and review of a variety of agreements (such as licensing, research, collaboration, distribution, confidentiality, service, consultancy and leasing contracts) • Support diverse range of legal department projects, e.g. contract templates, legal trainings, global guidelines and policies, global legal research projects, etc., and interact with Novartis global, regional and country legal network and other business stakeholders. #LI-Hybrid Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you’ll bring to the role • Education: Completed Master-level Law degree with above-average grades. Bachelor Law degree should be from Swiss university (sound Swiss law understanding required), Master-level Law degree can be from universities abroad (from Swiss university preferred) • Languages: Good German skills (B2) and English skills • Experience/Professional requirements: ideally, you have already gained your first professional or internship experience. Potential candidates should have an interest in legal issues in a major international corporation, pronounced commitment and the will and motivation to discover and learn new things. Please submit a cover letter that includes your motivation for the position and from when you will be available. Thank you. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture 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/networkDivision Legal Business Unit S&L 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 384220BR Oct 18, 2023 Switzerland About the Role Location: Fulltime, onsite in Basel, Switzerland #onsite Job Purpose: The Immunology Department (IMM DA) at Novartis is renowned for the discovery and development of B cell targeting therapies for the treatment of autoimmune and inflammatory diseases. We are looking for an experienced translational scientist for our growing B cell targeting Biologics portfolio, who will lead a lab for rapid indication expansion and asset differentiation. The candidate will also get the opportunity to lead antibody discovery projects and/or support clinical development programs. The ideal candidate is an expert translational scientist (PhD or MD/PhD), with broad scientific background and well-established expertise in B cell immunology. You will have a deep mechanistic understanding of autoimmune or inflammatory pathologies. Industrial experience in drug discovery of B cell targeting biologic therapies is beneficial. Responsibilities: • Lead pre-clinical drug discovery efforts for the treatment of immunological and inflammatory diseases • Perform mechanistic in vitro and in vivo studies to analyze the mode of action of novel therapies • Generate data for differentiation of B cell depleting mechanisms in autoimmune diseases and help designing superior B cell-targeted therapies • Provide scientific advice for preclinical and/or clinical projects and support biomarker and indication strategies. • Provide expert pharmacology support in external collaborations and for Investigational New Drug (IND) applications Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Key requirements: • Ph.D. in Immunology, Pharmacology, or related discipline plus >3 years of professional experience in academia or industry • Understanding of fundamentals and practice of the biologics drug discovery process from target validation and therapeutic concept through to clinical development. Industry experience is of advantage. • Publication track record in B cell immunology. Experience with novel B cell depleting therapies, incl. bi-/tri-specific antibodies for treatment of autoimmune diseases is of advantage. • Hands-on experience with in vivo models of immuno-inflammatory diseases • Excellent written and oral communication skills • Self-motivated and collaborative, with excellent time management and interpersonal skills Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more he re: https://www.novartis.com/about/strategy/people and culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits rewards Commitment to Diversity and 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/network 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.Division Biomedical Research Business Unit IMMUNOLOGY - 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 384218BR Oct 18, 2023 Switzerland About the Role Location: Full time, onsite, Basel, Switzerland #onsite Job Purpose: We are looking for a Principal Scientist level candidate to lead a lab in the in vivo Pharmacology group within the Immunology (IMM) Department. The successful candidate will have a Ph.D. and postdoctoral training in immunology and extensive experience working with mouse models to support drug discovery for treatment of immunologic and inflammatory diseases. The successful candidate is passionate for approaches to identify and validate novel targets using state-of-the art technologies. Responsibilities: The Lab Head will contribute to a strong and sustainable Immunology portfolio by: • Driving and supporting the identification of novel targets in collaboration with interdisciplinary project teams and disease focus groups (e.g. for joint inflammation) • Designing and implementing in vivo and in vitro studies to test the potency and selectivity of drug candidates in close interaction with chemistry teams • Elucidating the molecular mode of action of drugs in context of drug discovery projects • Investigating and developing in vitro/in vivo methods or technologies for the rapid advancement of drug discovery projects towards the clinic The candidate will collaborate with an interdisciplinary group of immunology scientists and associates to provide expert biology support to preclinical and clinical drug development projects for novel therapeutic agents. Commensurate with experience, the candidate will also provide biology expertise to late-stage clinical projects in a cross-functional setting. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you will bring to the role: • Ph.D. and 3-5 years of postdoctoral experience in immunology with a strong publication record • Expert understanding of in vivo disease models and experience in performing mechanistic studies in animal models of autoimmune and inflammatory diseases is required • Good understanding of state-of-the art methods to investigate cellular and molecular drivers of complex autoimmune and inflammatory diseases, such as psoriatic arthritis, lupus erythematosus, Sjögren`s disease and others • Profound understanding of pharmacological principles (e.g. target engagement) and experience in developing pharmacology assays for compound characterization are preferred • Curiosity, strong analytical and organizational skills and ability to work in interdisciplinary teams • Excellent oral and written communication and presentation skills in English * Restrictions on flexible working options may apply and will be discussed during interview if applicable. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more he re: https://www.novartis.com/about/strategy/people and culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits rewards Commitment to Diversity and 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/network 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.Division Biomedical Research Business Unit IMMUNOLOGY - 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 387196BR Nov 28, 2023 Switzerland About the Role The candidate will support our efforts in developing innovative cellular assays and microscopy readouts to better understand the mechanisms of human disease and to characterize molecules for treatment. Cellular assays at different levels of complexity, including 3D models, microtissues and co-cultures as well as aspects of mechanobiology are part of this project. Start date: 03/2024 Duration: 10 months Key responsibilities: • Development, optimization and applications of cell cultures in drug-discovery projects • Imaging of cellular models using fluorescent and bright-field microscopy • Interpretation of results #LI-Onsite Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Role Requirements • Education: Biology, pharmacology or bio-physics • Languages: English • Experience/Professional requirements: o Essential: Practical experiences in cell culture techniques o Essential: Microscopy (fluorescent, confocal or spinning-disk, brightfield) o Basic understanding of pharmacology (IC50, PK/PD, etc.) Desirable requirements: • Scientific understanding of Mechanobiology and Microfluidics Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. 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/networkDivision Biomedical Research Business Unit DSc 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 387624BR Nov 27, 2023 Switzerland About the Role 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 Head, HEOR and Patient-Centred Outcomes will impact millions of patients worldwide by enabling better patient outcomes and increased access and helping Novartis achieve its goal of providing world-class global access to medicine. This role will support Novartis International and will work with the International TAs to co-create impactful integrated product and evidence generation plans to support access and new commercial models. It is an International Value and Access leadership role and is critical for defining and crafting this newly reorganized function. Key responsibilities: • Leads Evidence Generation in relation to Health Care System and payer/access needs including the development and implementation of the next phase of the HEOR and PCO organization model, structure, vision and capabilities. • Provides effective and inspiring functional leadership for the HEOR and PCO team, actively works on career development for the team, and helps the team adjust to organisational change as we implement the new ways of working. • Works with International TA Heads to ensure appropriate resourcing for the highest prioritized programs and deploys resources according to changing needs and business impact. • Collaborates across business units to increase the influence of payer, access and healthcare systems voice and needs on the overall product and evidence generation strategies and activities across Novartis. • Shapes and ensures integrated evidence generation plans are continuously updated for prioritized products from entry to launch and throughout lifecycle management to deliver the value proposition necessary for access and optimal coverage. Also ensures development plans and protocols address payer and HCS needs for prioritized markets. • Commissions thoughtful and agenda setting pieces of work, working with a range of partners including think tanks and academic researchers to enable transformative approaches to evidence generation and value assessment • Establishes and maintains relationships with key economic modelling, outcomes research and access evidence talent and leaders in the field, both outside and inside the company; contributes to shaping the field on behalf of Novartis externally. • Collects learnings for HTA excellence, shapes HTA thinking externally and shares above therapy area insights with the organization by staying abreast of internal and external developments, trends and other dynamics that affect the HEOR and HTA domain. Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve. Role Requirements Essential requirements: • Advanced degree or equivalent education/degree in life science/healthcare required. PhD or equivalent preferred. • 12+ years of pharmaceutical industry experience • 5+ years people management and development experience in a matrix environment • Effective generation of timely Access / Payer / HEOR evidence to enable reimbursement and access in line with respective access and business strategy • HEOR & PCO capability building and implementation support. Driving perception of Novartis HEOR as industry leading with ability to shape the external thinking on HTA assessment and HEOR/PCO methodology • A strong leader, collaborator, integrator and team player with proven delivery of suitable HEOR, real-world evidence and clinical trial design for market access purposes Location: This role can be based in Switzerland or the UK. Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: Competitive salary, Annual bonus, Pension scheme, Share scheme, Health insurance, 25 days annual leave, Flexible working arrangements, subsidized dining facilities, Employee recognition scheme, learning and development opportunities. 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 Finance Business Unit Global Finance Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 United Kingdom Functional Area Market Access Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 381612BR Nov 28, 2023 Switzerland About the Role 500! The number of regulatory documents we authored last year. As a Regulatory Writer (Senior or Expert level, depending on experience) you will write and review high quality clinical and safety documentation for submission to regulatory authorities. As an Expert Regulatory Writer you also 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. Location: Basel, Switzerland #LI-Hybrid Your responsibilities: Your responsibilities include, but are not limited to: • To author and review high quality clinical and safety documents: non-registration Clinical Study Reports (CSR), Development Safety Update Reports (DSUR), Risk Management Plans (RMP). • Lead for outsourced Narrative projects. Coordinate other outsourced activities in RWS. • Core member of Clinical Trial Team (CTT) / participate in Safety Management Team(SMT). • Actively participate in planning of data analyses and presentation used in CSRs. • Act as documentation consultant in CTTs and SMTs to ensure compliance of documentation to internal company standards and external regulatory guidelines. • May act as Program Writer ensuring adequate medical writing resources are available for assigned program and consistency between documents. • Act as liaison between CTTs and publishing teams to ensure timely delivery of final documents for publishing. • Support the development of RWS through participating in RWS workstreams and other related activities. • Contribute to development of processes within RWS. May contribute to cross-functional initiatives. • Fostering cross-functional communication to optimize feedback and input towards high quality documents. • Maintain audit, SOP and training compliance. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements • Minimum university life science degree or equivalent is required. Advanced degree or equivalent education/degree in life sciences/healthcare is desirable. • 2- 6 years medical writing experience or other relevant pharma industry experience combined with scientific and regulatory knowledge, plus strong knowledge of the medical writing processes. • Knowledge & experience in global regulatory environment and process (key regulatory bodies, key documents, approval processes, safety reporting requirements). • Knowledge of process and some experience in global registering of drugs (simple submissions). • Excellent communication skills (written, verbal, presentations) • Very good understanding of biostatistics principles. • Ability to prioritize and manage multiple demands and projects. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 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/networkDivision Development Business Unit GCO 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 385036BR Nov 24, 2023 Switzerland About the Role Location: Basel, Switzerland About the role: At Novartis, we are reimagining medicine to improve and extend people's lives. We discover and develop breakthrough treatments and find new ways to bring cures to as many people as possible. Without safe, easy-to-use, high-quality drug delivery systems our patients could not get their medicines. This is where you come in ; the Device Technology Solution Center needs you as Senior CAD Designer for the development of drug device combination products working alongside our talented, bright and diverse teams. Our Device Technology Solution Center drives the technical development of drug delivery systems including needle safety devices, inhalers, auto-injectors, pen-injectors, on-body pumps, and ophthalmic drug delivery. We closely collaborate with project management, human factors engineers, packaging experts, analytical testing, production, external partners, regulatory experts and many more. The aim is to develop and/or integrate innovative drug delivery systems with the drug formulation and provide the necessary compliant technical documentation for health authorities and production. Your Responsibilities: • Work on Platform development and participate to project activities in cross-functional teams for easy-to-use, safe and robust products • Participate to the complete development process of medical devices (ideation, brainstorming, prototyping, manufacturing scall-up) • Create and review IP. • Manage and maintain CAD, 3D and drawings • Create, manage and maintain Tolerance Analysis. Size and specify plastic and metallic components • Work with third party suppliers, including prototyper, tool makers, CMOs • Write key design history file documents, e.g. design input requirements, component specifications and design verification documents. Ensure device design development is delivered to a high quality • Lead testing and characterization for acceptance, compliance, performance etc., and suggest improvements • Perform root cause analysis and develop robust solutions to prevent re-occurrence. Ensure components are delivered and controlled to the required quality for clinical trials and commercial production Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Role Requirements • Degree in mechanical engineering or equivalent • Preferably 10 years of experience in medical device development • Proficient spoken communication and excellent technical writing skills in English • Experience in designing plastic and metal components; tolerance analysis; metrology; lab testing • Experience in material qualification • Good knowledge in design for manufacturing and assembly • Good knowledge in key regulations and standards (e.g. ISO23098, ISO 11608, ISO 10993, MDR, Design Controls) • Design History File documentation • Ability to interact with cross functional team in matrix organization Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and 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/network 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.Division Development Business Unit TECHNICAL R & D GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 384175BR Oct 17, 2023 Switzerland About the Role Location: Full-time onsite, Basel, Switzerland. #onsite Job Purpose: 1 out of 10 people are suffering from immunological diseases. The Immunology Research 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, Immunology Research is seeking an experienced and highly motivated Senior Principal Scientist to drive new drug discovery projects and contribute to the development and positioning of Novartis’ B cell-depleting or modulating therapies. Your Responsibilities: You will be responsible for leading a state-of-the-art laboratory of scientists to discover and develop innovative therapies to treat B cell-mediated autoimmune diseases. You will provide biology expertise to drive discovery activities aimed at identifying novel therapeutic approaches with a focus on biotherapeutics and supporting development programs with pre-clinical and clinical B cell modulating assets. • Develop innovative ideas and lead early drug discovery projects within multidisciplinary teams up to clinical proof-of-concept studies in patients • Contribute to translational research activities and mechanism of action studies to support ongoing clinical development programs with advanced B cell-modulating programs • Contribute to the selection and strategic positioning of novel B cell modulating therapeutics • Evaluate external opportunities as part of cross-functional teams • Contribute to scientific publications, presentations as well as engagement with key opinion leaders Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you will bring to the role: • PhD degree and postdoc training in immunology, autoimmunity, immuno-oncology, oncology or related field with a minimum of 5 years of experience in the pharmaceutical/biotech sector • Deep knowledge of human B-cell immunology and B cell-mediated diseases (including but not limited to autoantibody-driven disorders) • Knowledge and experience in drug discovery and development of biotherapeutics including multi-specific antibodies. • Strategic and critical thinking in drug discovery with proven capacity to evaluate external opportunities as part of cross-functional teams • Significant scientific accomplishments and successful collaborations documented by publications in high-impact journals • Experience in leading and mentoring associates and cross-functional teams • Excellent organization, communication, presentation and analytical skills Desirable requirements: • Knowledge of B cell depleting modalities and experience in characterization of B cell modulating monoclonal antibodies and/or multi-specific cell engagers (e.g. T cell engagers) is a great plus Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people and culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits rewards Commitment to Diversity and 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/network *Restrictions on working flexibility may apply to this position and can be discussed at interview as required 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.Division Biomedical Research Business Unit IMMUNOLOGY - 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 385246BR Oct 31, 2023 Switzerland About the Role Applications are encouraged for a Research Scientist level candidate in the Biochemistry group of the Oncology department of Novartis' Biomedical Research division in Basel, Switzerland. Your role will be to contribute to the identification and characterization of chemical entities that will become anticancer drugs of the future. We seek for an experienced and motivated Research Scientist associate who will contribute in pushing the boundaries of innovation with bold science by supporting in biochemistry different projects in the new and growing field of radioligand therapy (RLT). Your Responsibilities: • Development of novel biochemical/biophysical assays using a wide range of technologies • Contribution to functional characterization of proteins targets • The work that will be carried out is centered around the profiling compounds/peptides and characterization of their mechanism of action. Albeit, activities will be in the RLT area, only non-radioactive compounds will be used • Work in teams in a multi-disciplinary environment and across multi-sites Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you will bring to the role: • Master’s degree (or equivalent) with good knowledge in Biochemistry/Biophysics. Please note that we do not require a PhD/Postdoc level candidate for this position. • Previous laboratory experience in a similar position in a drug discovery environment will be advantageous • Good hands-on experience in conventional assay technologies used in drug discovery (e.g. TR-FRET, FP) and biophysical methods particularly SPR • Experience in protein-ligand interactions and data analysis with standard curve fitting • Knowledge in lab automation (small laboratory workstations) • Fluent in English (German or French speaking in addition would be an advantage) Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people and culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits rewards Commitment to Diversity and 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/network *Restrictions on working flexibility may apply to this position and can be discussed at interview as required 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.Division Biomedical Research 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 386704BR Nov 15, 2023 Switzerland About the Role You will lead quarterly earnings process, including drafting press release and compiling interim financial report and analyst presentation and manage editing process for all materials, incorporating input from across the organization and ensuring message consistency and coherence. Leading implementation of investor relations communications for specific region and manage support of senior management from ECN and divisions so they are aware of, and well prepared for all elements of communication with investor and analyst community. Also you will monitor external trends & macroeconomics by providing meaningful regular analysis and critical evaluations to be used by senior management and translate existing data into relevant information for senior management and Board Key Responsibilities: • Draft press release and compiling interim financial report and analyst presentation. • Provide perspective on all investor communications, including annual report and other financial releases, helping craft and advance the Novartis story to address investor perceptions and needs. • Proactively, in rapid time, analyze, prepare and communicate on market moving events to investor community for specific region • Strengthen relationships with our current shareholders through creation and execution of account plans, and expand our shareholder base through identification of new potential targets. • Address inquiries from investors and analysts in a timely manner, providing accurate and balanced information on a range of topics from financial to product-specific. Deliver aligned messages that support the Novartis equity story. • Actively support Head of IR on specific projects (e.g. on presentations, analytics) • Serve and liaise with internal Divisions and work proactively to deliver high quality, accurate messages for both IR team and Senior Management to use with investors and analysts. • Plan and support execution of senior management roadshows, bank conference participation, one-to-one meetings and other investor events, including capital markets days (Meet Novartis Management & R&D days) • Capture investor/analyst feedback and share with IR team and appropriate management. • Follow financial market and benchmark Novartis activities vs. peers to inform our IR strategy and messaging. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you'll bring to the role: ESSENTIAL CRITERIA: • Ideally medical or science basic degree + MBA or finance (e.g. CFA) • Extensive experience within either IR and finance and ideally the healthcare industry; investment banking, research analyst or asset management with healthcare background • Excellent financial knowledge (BPA, FRA) • Proven ability to handle a range of complex issues/multiple projects simultaneously • Proven ability to effectively build and maintain relationships across all organizational levels • Excellent English oral/written communication skills Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards 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 re-quest 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 Finance Business Unit Global Finance 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 371158BR Nov 27, 2023 Switzerland About the Role 100,000+ That’s how many patients participate in our clinical trials at any given time. GCO is Novartis’ powerhouse of Global Clinical Operations, redesigned to enable faster trial recruitment and enhanced trial delivery resulting in more timely access for patients to potential novel treatments. Every day, we are the link between science and medicine – imagine the impact you could have as Clinical Operations Program Head! #GCO This role will be part of the GCO Selection University approach. If you wish to apply for any more Selection University positions, please make sure you do so within the same day to ensure your applications can be reviewed jointly by the selection panel. The Clinical Operations Program Head (COPH) is accountable to deliver data-driven, actionable operational and strategic insights for execution of a clinical development program and all associated trials by representing GCO at the Global Clinical Team (GCT) as well as at the Global Program Team (GPT). The COPH actively contributes to the GPCH’s and GCT’s strategic objective to achieve their own overall accountability for delivering the clinical program. The COPH provides the operational perspective to the Clinical Development Plan and to trial protocol design, ensuring that GCT/GPTs are aware of operational considerations and options, and that these are adequately reflected in planning. The COPH is the single point of contact for a trial/program within GCO and partners closely with key members of the GCT/GPT such as GPCH, GPH and other key communities to ensure best collaboration with operations to drive overall success of our programs and trials. The COPH leads the GCO sub-team to determine the GCO operational input to planning prior to any given development tollgate and to prepare the Operational Execution Plan (OEP), which is authored and owned by the COPH. The OEP incorporates both data-derived insights as well as country insights which enable informed decision-making, identify complexity, enable the generation of risk mitigation plans to reduce chances of delays, allow easier adaption of actions, and ensure transparency of the GCO operational position and the downstream delivery of program and trial milestones. Experienced leader guiding members of the organization through the GCO organizational evolution, the evolution of new “product aligned” ways of working and of our overall culture. He / she champions a product oriented agile mindset, fostering a culture of experimentation combined with accountable delivery and overall high performance. Your Key Responsibilities: 1. Accountable for the operational delivery of the clinical development program and is responsible for the overall operational execution of the clinical program and related trials, as aligned with the IDP/CDP. 2. Single GCO point of contact for assigned clinical development program and related trials. 3. Key partner to GPCH during strategy, planning and execution stage of the program and related trials ensuring that the clinical science and strategy are consistently harmonized with an operationally feasible approach within the OEP-defined operational boundaries, so that the trials generate reliable information to answer the research questions and support decision making while protecting study participants. 4. In partnership with GCPH and other GCT members, actively offer operational insights and options to contribute to the program and trial strategy, in particular with respect to study design and protocol optimization and timelines planning. 5. Leads the GCO sub-team to ensure the creation of best-in-class OEPs and to ensure that progress of the assigned programs and trials is on track and that operational risks are identified and mitigated proactively. The COPH further leads the GCO sub-team to ensure monitoring of the status of the progress of the clinical trials in line with the OEP and to deploy mitigation measures whenever needed to ensure overall trial success. 6. Leads the GCO sub-team taking accountability for the success of the team and of each team member by implementing “agile” and “product-oriented” ways of working. 7. Holds accountability for the operational delivery of the assigned program and related clinical trials and for all related strategic planning, prioritization of activities within that program. 8. Is a key contact to senior leaders in GCO and beyond. Empowered to manage stakeholders, resolve conflict, and facilitate agreements Diversity & Inclusion / EEO Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What You’ll Bring to the Role: • Bachelors in life science/healthcare required; Advanced degree or equivalent education/degree in life sciences/ healthcare preferred (PhD/MD/ PharmD/ Masters). • Fluent English (oral and written) • 10 or more years of experience in pharmaceutical clinical drug development. • Experience in managing associates globally and in management in a matrix organization. • Proven ability to lead cross functional matrix teams applying product-oriented agile ways of working. • Strong leadership, interpersonal and problem-solving skills. High resilience and ability to advocate and implement new ways of working. • Has ability to understand data and insights with ability to communicate this succinctly and accurately • Extensive knowledge of clinical development processes, preferably extensive knowledge of Novartis late-stage development processes or high likelihood to develop it within 6 months after appointment. • Proven ability to lead in times of organizational transformation and to lead across organizational boundaries. • Strong organizational awareness and stakeholder management skills. • Strong knowledge of therapeutic area or high likelihood to develop it within 6 months after appointment. Strong matrix management skills for bridging stakeholders (business, scientific, technical) • Strong relationship-building skills; can influence, negotiate with and motivate executive leadership • Strong tolerance for ambiguity, willingness to adapt, willing to speak-up and challenge • Embraces a culture of diversity, inclusion, quality, innovation and driving forward with integrity at all times Why Consider Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity, and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration and empowers our people to unleash their full potential. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity, and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying!Division Development Business Unit GCO GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 India Alternative Location 2 United Kingdom Alternative Location 3 Ireland Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 384486BR Oct 30, 2023 Switzerland About the Role 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 Discovery Bioanalytics Lab, in the Pharmacokinetic Sciences (PKS) department, is looking for a scientific associate with a strong background in the field of mass spectrometry to join their group in Basel, Switzerland. You will be part of a dynamic BA Labs team, deeply engaged in progressing drug discovery programs. In this role, you will contribute to the pharmacokinetic understanding of small molecule and peptide targets and the development of suitable methods, as part of the optimization and characterization process of candidate compounds of therapeutic relevance. While closely interacting with your lab head and colleagues in the group, you will work independently and flexibly contribute to local and global projects, while proactively sharing learnings, knowledge, and experience across global inter-disciplinary teams. Major accountabilities include: • Generation of novel, high quality data, using LC-MS/MS approaches • Independently design, generate, interpret and consolidate/report data of the respective experiments • Interface with multiple teams across expertise groups within PKS, including other Drug Discovery teams, as well as across the whole NIBR organization • Be an active team member in the automation of laboratory processes • Maintain high quality, detailed records within electronic laboratory notebook • Support generally shared lab activities and instrument maintenance Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements • Lab Technician or BSc or MSc or FH in Bioanalytical Chemistry or relevant discipline, with a minimum 3 years of industrial lab experience • Hands-on experience in LC-MS/MS method development and sample analysis • Experience in laboratory automation would be an advantage • Experience managing high volume assays • Proven ability to be a self-motivated team player able to thrive in a dynamic matrixed working environment • Excellent communication skills • Fluent in English (oral and written), German skills 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 Biomedical Research 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 384905BR Oct 30, 2023 Switzerland About the Role 6000! That’s the number of associates in the Novartis BioMedical Research (BR). This division is the innovation engine of Novartis, focusing on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. Your responsibilities: Your responsibilities include, but are not limited to: • Plan, design and conduct in vivo pharmacokinetic (PK) studies in rodents and non rodents, in order to support preclinical discovery projects across Novartis BioMedical Research portfolio. These studies can be done either internally or outsourced at External Service Providers (ESP). • Monitor, document, report and archive experimental details of these studies based on ALCOA+ principles in a timely and efficient manner and according to project timelines with a high level of quality, integrity, and ethics. • Manage actual study timelines and resources, ensure accuracy of study data within corporate databases and project tracking tools. • Maintain a well-organized laboratory environment, optimize laboratory workflows and ensure efficient use of resources. • Independently recognize challenges (technical, scientific or study related) and provide relevant input for solution/problem solving. • Comply with Swiss and Novartis-specific rules and regulations (e.g., Swiss Animal Welfare law, 3R principles, HSE regulations). • Be a pro-active, innovative, and solution-oriented team player, actively contributing to method development and refinements. • Overall, excellent collaboration, coordination, and communication skills with other scientists and within our matrix organization are required. Fostering an atmosphere of mutual respect. *Some restrictions on flexible working options will apply and will be discussed during interview if applicable. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you’ll bring to the role: • BSc or MSc degree in Biology or a related scientific discipline or completed apprenticeship as laboratory technician with at least 5 years of work experience, preferably in the area of DMPK in pharmaceutical, biotechnology industry, or CROs. • Several years of working experience in animal experimentation is a must (e.g., valid accreditation with LTK1 course, FELASA Cat. B training or equivalent training). • Good knowledge of in vivo techniques, instrumentation, and underlying principles within in vivo PK field (anatomy, anesthesia, surgery, dosing, and sampling techniques, ...). Experiences in non-rodent PK and PK/PD studies are considered as beneficial. • Good understanding of the pharmacokinetic science and the drug discovery and development processes. • Competency and interest in working with different IT systems and advanced computer literacy (MS Teams, MS Office, etc.) • Curious mindset, with high interest to continuously learn, implement and/or optimize new or existing experimental methods. • Team player with excellent communication and a collaborative mindset. Excellent oral and written communication skills in English is a must; some knowledge of German considered beneficial. 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. We are Novartis. Join us and help us reimagine medicine.Division Biomedical Research 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 384547BR Oct 16, 2023 Switzerland About the Role 2 Billion plus people are affected by diseases of the nervous system having a dramatic impact on patients and families around the world. Neurologic and psychiatric diseases remain as some of the largest challenges in medicine. Novartis is committed to changing the landscape by developing transformative treatments for important neuroscience disorders. As part of the Neuroscience (NS) departments at Novartis, you will help to develop therapies for patients with neuroimmunological disorders including multiple sclerosis. You will provide medical and scientific leadership and expertise in a role that significantly affects the entire Novartis NS 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. • 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 BioMedical Research and Development boards, and other Novartis Boards as required. • Evaluate clinical centers and foster communication with crucial collaborating investigators, regulatory authorities, and other stakeholders The work environment is in a matrix structure with cross-functional members from Translational Medicine, Biomedical Research and Development. 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 Neuroimmunology, you drive the project team clinical strategy. Works globally across various Novartis divisions as well as country organizations as appropriate Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you will bring to the role: • Medical Degree and advanced training in neuroimmunology • An expertise in translational or laboratory research. PhD preferred but not required • 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) 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 Biomedical Research 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 387446BR Nov 28, 2023 Switzerland About the Role We are looking for highly motivated Postdoc to support and further expand Novartis Oligonucleotide capacities in our Chemical and Analytical Development (CHAD) department Mixed Modality Unit. This Postdoc position is a unique opportunity to work in the field of oligonucleotide sciences in the Pharmaceutical industry with exposure to cutting-edge technologies at the interface between research and development. In alignment with Novartis ambition to become a global leader in environmental sustainability, the candidate will have the chance to positively impact the carbon footprint of Novartis. The candidate will not only be able to transfer know-how into practice, but also to develop soft skills and grow internal network for a future career in the Pharmaceutical industry. Preferred start date: February 1, 2024 Duration: 18 months Your responsibilities: Your responsibilities include, but are not limited to: • Develop efficient and scalable oligonucleotide processes on relevant projects within Novartis portfolio across different scales. • Be part of the Oligo chemist / engineering team to develop and optimize syntheses used in process R&D. • Investigate various approaches for oligonucleotide synthesis and evaluate their potential by applying cutting-edge automated platforms. • Collaborate with diverse experts in the areas of Nucleic Acid Chemisty, Process Chemistry, Process Engineering and Analytics. #LI-Onsite Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you’ll bring to the role: • Completed PhD, preferably in Organic Chemistry and ideally with a focus on oligonucleotides • Hands-on attitude and passionate for technical solutions. • Experience in process development is a plus. • An excellent track record of original research and extensive experience in using “state of the art” technologies. • Fluency in English, additional German proficiency is a plus. • Ready to expand own knowledge, open minded with an international outlook. • Finally, since all work takes place in multidisciplinary project teams, strong interpersonal and communication skills are required Please submit a cover letter that includes your motivation for the position and from when you will be available. Thank you. Why Novartis? Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture 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/networkDivision 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 383915BR Oct 25, 2023 Switzerland About the Role Location: Basel, Switzerland About this role: This is a unique opportunity to join our Development Team as a Clinical Development Director (CDD) in the Cardio Renal & Metabolic (CRM) Development Unit. The CRM DU is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. As a CDD in the Renal TA, you will have oversight of the clinical development for the assigned programs and drive the 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. Key Responsibilities: • Providing clinical leadership and strategic input for all clinical deliverables in the assigned project or section of a clinical program. Clinical deliverables may include clinical sections of individual protocols or sub studies consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications • Leading development of clinical sections of trial and program level regulatory documents • Driving 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 • Overseeing/conducting ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead • Supporting (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section and may be a core member of the Safety Management Team, supporting overall program safety reporting in collaboration with Patient Safety • As a clinical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards • Contributing to scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for franchise medical/scientific training and may be the Program Manager of other associates Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Essential Requirements • Advanced degree in life sciences / healthcare (or clinically relevant degree) is required. • Fluent oral and written English • Minimum 7 years experience in clinical research or drug development • Working knowledge of the assigned disease area is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) or program level • Demonstrated ability to establish effective working relationship with key investigators • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes • Strong communication skills with the ability to work in a cross functional and global organization. Desirable Requirements: • PharmD or PhD is strongly preferred * Final job title (CDMD, Band 3 / Senior CDMD, Band 3) and associated responsibilities will be commensurate with the successful candidates’ level of expertise ***Some restrictions on flexible working options may apply and will be discussed during interview if applicable. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and 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 Development Business Unit CARDIO-RENAL-METAB GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 385607BR Oct 25, 2023 Switzerland About the Role Location: Basel, Switzerland (hybrid) 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 in the Renal TA, 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 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 We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you bring to the role: • MD or equivalent medical degree is required in addition to advanced knowledge and clinical training in medical/scientific area; Clinical practice experience 4 years (including residency) and board certification or eligibility in disease area 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. *Final job title and associated responsibilities will be commensurate with the successful candidates’ level of expertise (Senior/Director/Associate) **Some restrictions to flexible working models may apply and will be discussed at interview if applicable 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 Development Business Unit CARDIO-RENAL-METAB GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 385382BR Oct 25, 2023 Switzerland About the Role The Clinical Development Director (CDD) in the Cardiovascular, Renal & Metabolic (CRM) Development Unit is responsible for leading the strategic planning and management of the assigned clinical program(s) from an end-to-end clinical development perspective. This is a hybrid role based in Basel, Switzerland. As a CDD in the Renal TA, you will have oversight of the clinical development for the assigned programs and drive the 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. Main responsibilities of this role are: • Providing clinical leadership and strategic input for all clinical deliverables in the assigned project or section of a clinical program. Clinical deliverables may include clinical sections of individual protocols or sub studies consistent with the Integrated Development Plans (IDP), clinical data review, program specific standards, clinical components of regulatory documents/registration dossiers, and publications • Leading development of clinical sections of trial and program level regulatory documents • Driving 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 • Overseeing/conducting ongoing medical and scientific review of clinical trial data with Clinical Scientific Expert(s) with appropriate oversight from Medical Lead • Supporting (Sr.) GPCH in ensuring overall safety of the molecule for the assigned section and may be a core member of the Safety Management Team, supporting overall program safety reporting in collaboration with Patient Safety • As a clinical expert, supporting the (Sr.) GPCH or CDH in interactions with external and internal stakeholders and decision boards • Contributing to scientific training of relevant Novartis stakeholders on the disease area and compound/molecule. May serve as speaker for franchise medical/scientific training and may be the Program Manager of other associates Minimum Requirements • Advanced degree in life sciences / healthcare (or clinically relevant degree) is required. PharmD or PhD is strongly preferred*** • Fluent oral and written English • Minimum 7 years experience in clinical research or drug development • Working knowledge of the assigned disease area is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) or program level • Demonstrated ability to establish effective working relationship with key investigators • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes • Strong communication skills with the ability to work in a cross functional and global organization Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Minimum Requirements: • Advanced degree in life sciences / healthcare (or clinically relevant degree) is required. PharmD or PhD is strongly preferred • Fluent oral and written English • Minimum 7 years experience in clinical research or drug development • Working knowledge of the assigned disease area is desired with proven ability to interpret, discuss and present efficacy and safety data relating to clinical trial(s) or program level • Demonstrated ability to establish effective working relationship with key investigators • Working knowledge of GCP, clinical trial design, statistics, and regulatory and clinical development processes • Strong communication skills with the ability to work in a cross functional and global organization *Final job title and associated responsibilities will be commensurate with the successful candidates’ level of expertise. **Some restrictions to flexible working models may apply and will be discussed at interview if applicable Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You’ll receive: You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook. https://www.novartis.com/careers/benefits-rewards Commitment to Diversity and Inclusion / EEO: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. 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 Development Business Unit CARDIO-RENAL-METAB GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 386758BR Nov 20, 2023 Switzerland About the Role We are currently seeking a highly motivated and talented individual for an internship opportunity in the field of analytical method development for the characterization and quantification of oligonucleotides using liquid chromatography with inductively coupled plasma mass spectrometry (LC-ICP-MS). This is an exciting opportunity to contribute to cutting-edge research in the field of bioanalytical chemistry in pharmaceutical environment. Preferred start date 01.03. 2024 Duration: 5-8 months #LI-Onsite Key responsibilities: • Develop a method for the separation, detection and characterization of oligonucleotides using liquid chromatography with inductively coupled plasma mass spectrometry (LC-ICP-MS). • Validate and optimize the method for the analysis of oligonucleotides using in vitro samples from complex biological matrices (plasma, liver tissue etc). • Evaluate potential of this method for quantitative assessment of drug metabolites. • Apply developed ICP-MS method to real life in vivo samples of ongoing projects. Essential requirements: • Strong theoretical and scientific background in liquid chromatography (e.g. UHPLC, RP-HPLC), mass spectrometry (e.g. HRMS, MS/MS) and in sample preparation of biological fluids (e.g. SPE) and the openness to learn new techniques and deepen your knowledge. • Experience in using and maintaining analytical equipment (e.g. LC, MS) and the motivation to work in a laboratory environment with a team of dedicated scientists are considered essential for this role. • Hands-on experience with ICP-MS would be an asset • Proficiency in English, with German skills are advantageous. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements • Student currently enrolled in a Masters degree program in a Life Science discipline (e.g. Pharmacy, Chemistry, Food Chemistry, Biotechnology, Biochemistry or Bioengineering etc.) or recent graduate of a Life Sciences Master program looking to gain first experience Desirable requirements: • You have a creative mindset, a self-driven attitude, a high level of learning agility, you are eager to expand your knowledge and above all you value collaboration in teams. • You have strong problem-solving and critical thinking abilities. • Knowledge of analytical characterization methods for oligonucleotides is preferred. Why Novartis: Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture 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/networkDivision Biomedical Research Business Unit Translational Medicine Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to JobAccess Job Account

Job ID 384872BR Nov 20, 2023 Switzerland About the Role The Senior Manager M&A is responsible for helping the M&A Transactions team achieve key targets including outside-in evaluation, diligence, execution and signing of M&A transactions. The Senior Manager M&A will support M&A Project Leads, Deputy Head and Head of M&A Transactions on presentations, briefings and memos for senior management, the Executive Committee of Novartis, and the Board of Directors on M&A opportunities as well as ad-hoc BoD requests. In doing so, the Senior Manager M&A will act as a center of expertise for project management, ensuring high quality outputs in a timely manner. Your responsibilities include, but not limited to: Participate and support in the execution of Novartis’ M&A strategies and plans. This means:  Take the lead in preparation of project materials (kick-offs, M&A briefings, ECN presentations) under the guidance of Project Leads.  Responsible for ensuring that final presentations meet the highest quality standards in M&A, ensuring consistency in formatting, accuracy of content, and clarity of communications and messaging.  Support Project Leads, when requested, on end-to-end project management, remaining closely co-ordinated with M&A Finance.  Collaborate with Corporate Functions (Legal, Antitrust, P&O etc.) on M&A projects and provide sup-port to broader Corporate diligence activities.  Research public information, conduct industry research and competitive landscaping to facilitate M&A screening / assessments.  Keep abreast of M&A transactions in the industry, maintaining precedents and premia analysis for the team.  Participate in banker pitches, when requested, and maintain a log of ideas presented and feedback.  Contribute towards improving M&A processes and systems. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements • University Degree (Business, Finance, Accounting, Economics or any field with financial content) • Proficiency in English required. • Relevant professional M&A experience from investment banking/M&A advisory/consulting, corporate M&A or transaction services • Experience in the Pharmaceutical industry is a plus • Strong analytical skills with critical thinking abilities • Deep knowledge of valuation methodologies and financial analysis of public companies • Ability to conduct research and summarize key findings clearly. • Good understanding of key subjects such as accounting, tax, treasury, as it relates to M&A • Displays highest professionalism in an executive setting • Agility to work under pressure in an unpredictable and demanding environment • Resilience to achieve results in a structured and upright manner Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture You can find everything you need to know about our benefits and rewards in the Novartis Life Handbook - https://www.novartis.com/careers/benefits-rewards Novartis is committed to working with and providing reasonable accommodation to all individuals. If, be-cause 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 re-quest 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 Strategy & Growth Business Unit Strategy & Growth 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 383487BR Nov 08, 2023 Switzerland About the Role Diese Stelle beinhaltet die rechtzeitige Bereitstellung von Materialien für Batch Processing in Cell & Gene Therapies Stein in der richtigen Menge und Qualität, sowie Versand von Finished Product, Einlagerung und Auslagerung sowie die dazugehörigen Buchungen im SAP. Ihr Verantwortungsbereich: • Annahme von Warenlieferungen für Cell & Gene Therapies, insbesondere von biologisch gefährlichen Materialien • Einbuchung von Materialien in SAP • Einlagerung von eingehenden Materialien gemäss den GMP- und HSE-Anforderungen • Handhabung von Tiefkühltransportbehältern mit Flüssigstickstoff bei Annahme und Versand von menschlichen Zellen • Festgestellte Abweichungen beurteilen und mit Vorgesetztem weiteres Vorgehen besprechen • Bereitstellung und Verwendung von korrekten und geprüften Einsatzkomponenten • Sicherstellen einer termingerechten Abarbeitung der anfallenden Aufträge, Priorisieren von • Massnahmen zur Auflösung von Rückständen • Kommunikation mit der Produktionsplanung und der PU • Abstimmung der PU internen Ziele mit globalen Anforderungen Diese Stelle ist auf maximal 2 Jahre befristet. Benutzen Sie den folgenden Link, um sich das "Stein Cell&Gene: Innovation is teamwork" Video anzusehen: Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Ausbildung: • Abgeschlossene technische und/oder kaufmännische Ausbildung/Berufslehre. Sicherer Umgang mit SAP und MS-Office Anwendungen • Berufserfahrung in der pharmazeutischen Produktion, Produktionsplanung oder Logistik Sprache: • Deutsch in Wort und Schrift sehr gut • Englisch in Wort und Schrift min. Grundkenntnisse 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 Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 383488BR Nov 08, 2023 Switzerland About the Role Diese Stelle beinhaltet die rechtzeitige Bereitstellung von Materialien für Batch Processing in Cell & Gene Therapies Stein in der richtigen Menge und Qualität, sowie Versand von Finished Product, Einlagerung und Auslagerung sowie die dazugehörigen Buchungen im SAP. Ihr Verantwortungsbereich: • Annahme von Warenlieferungen für Cell & Gene Therapies, insbesondere von biologisch gefährlichen Materialien • Einbuchung von Materialien in SAP • Einlagerung von eingehenden Materialien gemäss den GMP- und HSE-Anforderungen • Handhabung von Tiefkühltransportbehältern mit Flüssigstickstoff bei Annahme und Versand von menschlichen Zellen • Festgestellte Abweichungen beurteilen und mit Vorgesetztem weiteres Vorgehen besprechen • Bereitstellung und Verwendung von korrekten und geprüften Einsatzkomponenten • Sicherstellen einer termingerechten Abarbeitung der anfallenden Aufträge, Priorisieren von • Massnahmen zur Auflösung von Rückständen • Kommunikation mit der Produktionsplanung und der PU • Abstimmung der PU internen Ziele mit globalen Anforderungen Diese Stelle ist auf maximal 2 Jahre befristet. Benutzen Sie den folgenden Link, um sich das "Stein Cell&Gene: Innovation is teamwork" Video anzusehen: Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Ausbildung: • Abgeschlossene technische und/oder kaufmännische Ausbildung/Berufslehre. Sicherer Umgang mit SAP und MS-Office Anwendungen • Berufserfahrung in der pharmazeutischen Produktion, Produktionsplanung oder Logistik Sprache: • Deutsch in Wort und Schrift sehr gut • Englisch in Wort und Schrift min. Grundkenntnisse 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 Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 385593BR Nov 30, 2023 Switzerland About the Role Process Expert CGT (temp), Stein, Switzerland 43 million! the total no of patients we reached in 2022 through our collective efforts to reimagine medicine and make a real difference to the lives of patients around the world. As a Jr Process Expert you will support PU by providing front line expert support for all process-specific issues to ensure execution of processes on time, continuously improving in quality and productivity, performed in compliance to cGMP, SOPs and applicable guidelines and functional standards. Your key responsibilities: Your responsibilities include, but are not limited to: · Provide front line support to manufacturing, working with the shift teams, focusing on manufacturing each batch safely, on time, in compliance with the batch instructions and quality requirements. · Responsible for maintaining the master manufacturing documents of assigned products (e.g. Master Batch Record, Bill of Material (BOM) & Recipe, Quality Risk Assessment, Zurich Hazard Analysis). · Ensure that all critical parameters are within written Instruction (i.e. Master Batch Record). · Support steward for assessment of technical changes and process changes (task manager ACC/PCC). · Ensure that all process changes are managed through appropriate change control procedure. · Execute process improvements and scale-up. · Ensure that technical batches generate sufficient process knowledge by thoroughly testing critical variables. · Support technology trainings and education programs for production operators. · Act as Subject Matter Expert for Audits. We offer a temporary position with a max. 2 year duration. Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements What you’ll bring to the role: · Desirable BSc. in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy with further qualifications in Production Management or equivalent. · Fluent in English/proficiency in German. · Desirable: previous experience in process support role on the shop floor of GMP manufacturing and/or QA/QC. Why Novartis? Our goal is to reshape medicine to improve and extend people's lives, and our vision is to become the most valued and successful drug company in the world. How can we achieve this? With our employees. It's our people who drive us every day to achieve our goals. Be a part of this mission and join us! Learn more about: https://www.novartis.com/about/strategy/peopleandculture You will receive: Everything you need to know about our benefits and premiums can be found in the Novartis Life Handbook. https://www.novartis.com/careers/benefits 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 Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 381857BR Nov 30, 2023 Switzerland About the Role Scientist MS&T Location: Novartis, Stein, Switzerland About the Role: Purpose of this role is to design, plan, perform, interpret and report scientific experiments under the lead of the department head to contribute to overall MS&T strategies and objectives. Key Responsibilities: • Comply with applicable GxP regulations, SOPs, HSE, ISEC & other Novartis Guidelines in the laboratory; Maintain up-to-date documentation of laboratory work carried out including documentation storage and archiving; Contribute to and maintain lab instructions, SOPs, templates • Support, qualification and calibration of lab / pilot equipment with accompanying documentation, schedule and perform routine maintenance; Contribute to the evaluation of new equipment. • Evaluate and implement state-of- the-art technologies (laboratory methods, techniques), optimize existing methods, contribute to new method development and reproduce published methods; Owns and represents his/her area of responsibility in health authority inspections; Assess patent landscape with respect to specific project related questions • Design, execute and document experiments (formulation / analytical tests etc.) for products assigned in the context of process transfer, process improvement and process validation • Prepare and review appropriate GxP documentation including change requests; Support maintenance of QRAs, contribute to determination of process control strategy based on CQAs and where necessary on CPP, CMA to support ongoing process verification (OPV) • Provide scientific and organizational responsibility for managing project tasks; Plan and execute experiments to support production trials / method transfers and document results in reports; Actively support the transfer of analytical or manufacturing procedures to pilot plant or production. • Design, plan, execute and interpret scientific experiments in line with development manuals in order to deliver project timelines & targets, establish reports. Provide documentation of raw data, evaluation and contribute to interpretation of results. Provide input for the selection of next experiments - seek proactively for support and coaching from Project Leader or SME if necessary • Ensure that cost benefits are delivered according to targets; Support root cause investigation for deviations, OOS, OOT by designing and executing experiments, analyzing data & interpretation of results Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Essential Requirements: • University degrees (BSc or MSc) from chemistry, biologics, pharma or any other appropriate natural sciences • Preferable 3-year experience in the pharmaceutical environment (e.g. laboratory, production, synthesis). Adequate scientific or technical knowledge in a specific area (e.g. synthetic, analytical, galenical, biotechnological). • Awareness for safe handling of chemicals, potentially dangerous materials and equipment • Good knowledge of laboratory and/or technical tools • Basic presentation skills, good communication skills • Fluent in oral and written English and proficient in site local language You’ll receive: Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve. Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/en_US/networkDivision Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 383997BR Nov 15, 2023 Switzerland About the Role QC Analyst ll Location: Novartis, Stein, Switzerland About the Role: Why join Cell & Gene Therapy? Because in the Cell & Gene Therapy network we are operating on a daily basis (including weekend days) to deliver our lifechanging medicines the most rapidly to the patient. We are helped do this by facilities and infrastructure that are top class, but also by an environment that is open-minded, and one which supports people to develop with mentoring, training and the opportunity to experience different disciplines. This role is limited for 24 months. Key Responsibilities: • Plan and perform Bioassays (e.g. Flow Cytometry, ELISA) and qPCR assays of release testing • Perform all testing and activities compliantly following appropriate SOPs and procedures and maintain controls, reagents and reference standards to support testing • Review data generated by other team members. • Evaluate/qualify and maintain lab equipment and execute validation/transfers/optimization of test methods as per appropriate protocols • Contribute to OOS/OOE and deviation investigations; interface with regulatory agencies during audits; support 6S and Lean projects; continually identify areas for improvements in project work. • Knowledge of LabWare LIMS, SAP and/or other QC data systems • Maintain GMP quality systems; review of laboratory logbooks and laboratory cleaning; performing daily equipment startup and PQ; assure stock of reagents and materials Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Essential Requirements: • Education - BA in biology, chemistry, biochemistry, microbiology or other related science • 0 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry • Biological techniques (Flow Cytometry, ELISA, qPCR, Cell Count...) • Thorough knowledge of cGMP requirements • Results oriented, team player and able to work with all levels of the organization • Strong written and verbal communication skills are essential • Fluent in English language, German desirable You’ll receive: Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well. You’ll have to work on a shift model. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve. Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/en_US/networkDivision Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 382848BR Sep 19, 2023 Switzerland About the Role QC Analyst I – BET Analytik und/oder Wasseranalytik Lokation: Novartis, Stein, Switzerland Die Position: Als Teil der Qualitätskontrolle spielst du eine Schlüsselrolle bei der Analytik des wichtigsten Hilfsstoffes – Wasser – all unserer sterilen Produkte und trägst zur höchsten Produktqualität für Millionen von Patienten in mehr als 150 Ländern auf der ganzen Welt bei. Es handelt sich hierbei um eine Einstiegsposition Ihr Verantwortungsbereich: • Organisation, Durchführung, Auswertung und Dokumentation der Analytik von Wasser mit Hilfe physikalisch-chemischer, biologischer und mikrobiologischer Tests bzw. Analytik von Bakterien-Endotoxinen in Ausgangsstoffen, Wirkstoffen und Prodrukten • Einhaltung und Überwachung der cGMP-Regeln, SOPs (Standardarbeitsanweisungen) und Sicherheits-Vorschriften Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Was Sie zur Rolle mitbringen: • Abgeschlossene Lehre als Laborant/in oder äquivalente Ausbildung • erste Erfahrung im Bereich Qualitätskontrolle und/oder im GMP/GxP Umfeld wünschenswert • Sehr gutes technisches und analytisches Verständnis • Ausgeprägtes Qualitätsdenken und gewinnende Kommunikationsfähigkeit im Umgang mit verschiedenen internen Ansprechpartnern • Fliessend Deutsch in Wort und Schrift. • Teamplayer, exakte und selbständige Arbeitsweise • Hohe Eigenverantwortlichkeit und hohe Lernbereitschaft Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Engagement für Vielfalt & Inklusion Novartis ist bestrebt, ein hervorragendes, integratives Arbeitsumfeld und ein vielfältiges Team aufzubauen, das die Patienten und Gemeinschaften, denen wir dienen, repräsentiert. Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Regular Shift Work No Apply to JobAccess Job Account

Job ID 352828BR Sep 19, 2023 Switzerland About the Role Cell Processing Specialist CGT (Temporary) Novartis, Stein, Switzerland 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 key responsibilities: 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. Role Requirements What you’ll bring to the role: • 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 You’ll receive: Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve. Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/en_US/networkDivision Operations Business Unit CELL & GENE THERAPY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Technical Operations Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account

Job ID 386432BR Nov 24, 2023 Switzerland About the Role Prozessmitarbeiter Lokation: Novartis, Stein, Switzerland Die Position: Seit 1957 und nunmehr 66 Jahren werden in Stein Medikamente produziert, kontrolliert, verpackt und weltweit versandt – pro Jahr aktuell rund 2 Milliarden Tabletten, Kapseln, Ampullen, Fertigspritzen, Vials und Autoinjektoren. Novartis Pharma Stein AG ist eines der bedeutendsten pharmazeutischen Produktionswerke von Novartis - werden Sie Teil davon - wir suchen derzeit einen Prozessmitarbeiter. Diese Stelle ist auf 2 Jahre ausgeschrieben. Ihr Verantwortungsbereich: • Herstellung Pharmazeutischer Darreichungsformen (Tab, FCT, Kap,) und Dokumentationen im MES • Durchführung von Anlagen- und Raumreinigungen entsprechend der SOPs • Führt einfache Wartungsarbeiten eigenständig durch, kann kleinere Störungen beheben. • Selbständige Re- und Demontagen von Anlagen und deren Peripherien sowie dem dazugehörenden Werkzeugwechsel. • Unterstützung bei der Erstellung und optimierung von Herstellvorschriften und Arbeitsanweisung (MBRs & SOPs) • Fachlicher Support bei der Erstellung der Anlagerezepte. • Durchführung der delegierten Musterzüge • Einarbeitung von neuen Prozessmitarbeitern an den entsprechenden/zugeteilten Prozessanlage Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Was Sie zur Rolle mitbringen: • Organisatorisches Verständnis • Teamfähigkeit sowie gute Kommunikationsfähigkeiten • Verhandlungssicher in Deutsch • Gutes Prozess und Qualitätsverständnis • Erfahrung im Bedienen von Maschinen • Ausbildung oder langjährige Erfahrung im GxP regulierten Umfeld bzw. in der Pharmaproduktion oder vergleichbar wie Lebensmittel oder Chemischerproduktion als Vorteil • Erfahrung mit MES Systemen wie ATLAS und PAS X und Limos sprich PMX und SAP Kenntnisse als Vorteil • Englisch Kenntnisse als Vorteil Warum Novartis? Über 766 Millionen! - so viele Leben haben wir im Jahr 2021 mit unseren Produkten erreicht. Und während wir darauf stolz sind, stellen wir uns ständig die Frage: Wie können wir in einer Welt des digitalen und technologischen Wandels noch mehr Leben verbessern und verlängern? Wir glauben, dass an der Schnittstelle von medizinischer Wissenschaft und digitaler Innovation neue Erkenntnisse, Perspektiven und bahnbrechende Lösungen gefunden werden können und dass ein vielfältiges, gleichberechtigtes und integratives Umfeld zu neuen Arbeitsweisen inspiriert. Wir sind davon überzeugt, dass unser Potenzial in einer von Integrität, Neugier und Flexibilität geprägten Kultur gedeihen und wachsen kann. Und wir können neu erfinden, was möglich ist, wenn wir mit Mut zusammenarbeiten, um die schwierigsten medizinischen Herausforderungen der Welt offensiv und ehrgeizig anzugehen. Denn das größte Risiko im Leben ist das Risiko, es nie zu versuchen! Stellen Sie sich vor, was Sie hier bei Novartis tun könnten! Engagement für Vielfalt & Inklusion Novartis ist bestrebt, ein hervorragendes, integratives Arbeitsumfeld und ein vielfältiges Team aufzubauen, das die Patienten und Gemeinschaften, denen wir dienen, repräsentiert. Zugänglichkeit und Unterbringung Der Novartis Konzern ist bestrebt, mit allen Personen zusammenzuarbeiten und ihnen angemessene Vorkehrungen zu bieten. Wenn Sie aufgrund einer Erkrankung oder Behinderung eine angemessene Vorkehrung für einen Teil des Einstellungsverfahrens benötigen oder um detailliertere Informationen über die wesentlichen Funktionen einer Stelle zu erhalten, senden Sie bitte eine E-Mail an [email protected] und teilen Sie uns die Art Ihrer Anfrage und Ihre Kontaktdaten mit. Bitte geben Sie in Ihrer Nachricht die Nummer der Stellenausschreibung an. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Stelle nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber in Verbindung bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, werden Sie hier Mitglied des Novartis Netzwerks: https://talentnetwork.novartis.com/en_US/networkDivision Operations Business Unit 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 384435BR Nov 03, 2023 Switzerland About the Role QC Analyst ll Location: Novartis, Stein, Switzerland About the Role: Why join Cell & Gene Therapy? Because in the Cell & Gene Therapy network we are operating on a daily basis (including weekend days) to deliver our lifechanging medicines the most rapidly to the patient. We are helped do this by facilities and infrastructure that are top class, but also by an environment that is open-minded, and one which supports people to develop with mentoring, training and the opportunity to experience different disciplines. This role is limited for 24 months. Key Responsibilities: • Plan and perform Bioassays (e.g. Flow Cytometry, ELISA) and qPCR assays of release testing • Perform all testing and activities compliantly following appropriate SOPs and procedures and maintain controls, reagents and reference standards to support testing • Review data generated by other team members. • Evaluate/qualify and maintain lab equipment and execute validation/transfers/optimization of test methods as per appropriate protocols • Contribute to OOS/OOE and deviation investigations; interface with regulatory agencies during audits; support 6S and Lean projects; continually identify areas for improvements in project work. • Knowledge of LabWare LIMS, SAP and/or other QC data systems • Maintain GMP quality systems; review of laboratory logbooks and laboratory cleaning; performing daily equipment startup and PQ; assure stock of reagents and materials Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements Essential Requirements: • Education - BA in biology, chemistry, biochemistry, microbiology or other related science • 0 - 5 years of experience in the pharmaceutical, biologics, microbiology, sterile manufacture, or medical device industry • Biological techniques (Flow Cytometry, ELISA, qPCR, Cell Count...) • Thorough knowledge of cGMP requirements • Results oriented, team player and able to work with all levels of the organization • Strong written and verbal communication skills are essential • Fluent in English language, German desirable You’ll receive: Breakdown of benefits received in this role. Include flexible working, learning and development opportunities as well. You’ll have to work on a shift model. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world's toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Commitment to Diversity & Inclusion Novartis is committed to building an outstanding, inclusive work environment and diverse team's representative of the patients and communities we serve. Accessibility and accommodation Novartis group is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in order to receive more detailed information about the essential functions of a position, please send an e-mail to [email protected] and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/en_US/networkDivision Operations Business Unit QUALITY Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Quality Job Type Full Time Employment Type Temporary Shift Work Yes Apply to JobAccess Job Account