Novartis Pharma AG

Job ID 393748BR Apr 02, 2024 Switzerland About the Role We are offering a 6-months legal trainee position to support the Novartis Operations Legal department on a wide range of legal matters and projects in areas such as contract law, commercial law, M&A and licensing transactions, restructuring, antitrust law etc. This legal trainee position offers excellent opportunities to gain first-class, hands-on in-house legal experience within the stimulating, multinational environment of a leading pharmaceutical company. Duration: June 1, 2024 - November 30, 2024 Your responsibilities will include: • Support M&A and corporate projects, manufacturing and supply agreements, real estate projects, portfolio and manufacturing site divestments, including conducting due diligence, managing data rooms and enquiries in the sale process, and legal project management • Support a diverse range of commercial matters relating to the development, procurement, manufacturing, quality assurance and supply chain and distribution of pharmaceutical products • Support diverse range of legal department projects, e.g. contract templates, legal trainings, global legal research projects, digitalization, outsourcing etc. • Assist in drafting, negotiation and review of a variety of transactional, commercial and technical agreements • Draft legal memoranda on a wide variety of legal issues and disputes • Provide legal advice to internal clients, draft documents and key position summaries • Interact with Novartis global, regional and country legal network #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: Swiss Law degree (BLaw plus MLaw or equivalent) • Languages: Business-level English (written and spoken); German ideally and additional languages are a plus • Experience/Professional requirements: o Prior legal professional experience in a law firm, court or legal in-house department (internships etc.) would be helpful. We are also open to applicants without prior experience who have a strong interest and are motivated to learn on the job o Overall high motivation and ability to work independently Desirable requirements: • Other professional experience in the corporate environment is a plus Please submit your complete application (CV, cover letter and your academic records) online. In your cover letter, please include your motivation for the role and if you are available to start in June 2024. Why Novartis Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? 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 diversity.inclusion_ch@novartis.com, and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division Operations Business Unit NTO LEGAL Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to Job(link is external)Access Job Account(link is external)

Job ID 388744BR Apr 11, 2024 Switzerland About the Role Location: Basel, Switzerland Role Purpose: We are searching for an Analytical Expert with a strong focus on Oligonucleotides to support Analytical Research & Development (ARD). ARD sits within the Technical R&D department of Development and plays a crucial role in the characterization and analysis of Drug Substances and Drug Products from the time they leave the discovery laboratory until they are transferred to Commercial Production. We are looking for a highly motivated and experienced Analytical Expert or Analytical Project leader with a strong background and experience in Oligonucleotide analytics. Your responsibilities: • You will help leading analytical activities within a Technical CMC project team (e.g., hep to define control and specification setting strategies for Drug substances and Drug products, method development, validation, stability, and release testing). You provide valuable input to the analytical CMC documents and support regulatory submissions. • Manage interactions and contribute to a high level of collaboration with internal and external stakeholders. • Write of analytical source documents (e.g Analytical methods, Specifications, Validation reports, Stability reports) • Lead outsourced analytical activities at CROs / CDMOs and contribute to manage the external partnership. • You will be responsible for shaping our Oligonucleotide lab further, together with well-experienced technicians. You will drive, lead, and manage analytical activities including impurity profiling related to the analytical development of Oligonucleotides (e. g. method development, validation, stability, and release testing). • You will be responsible to evaluate and implement new analytical methodologies with the aim of bringing the lab at the forefront of Oligonucleotide analytics. • Provide scientific guidance to the cross-functional and global project teams and thereby scientifically driving our exciting Oligonucleotide portfolio. • Display a collaborative and inspired attitude within the Oligonucleotide lab, project teams and stakeholders is key. 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: PhD in analytical chemistry or equivalent and a minimum 3 years’ experience in the pharmaceutical industry in analytical development, preferably in development of sterile parenteral products. Strong expertise in the field of oligonucleotide analytics. • Profound knowledge in analytical separation techniques such as liquid chromatography (RP, IEX and HILIC) is a must. Experience in method development and troubleshooting. Experience in developing control strategies. • Profound expertise in Mass Spectrometry (ranging from mass confirmation to actual quantitative analysis of impurities and sequencing) is a plus. • GMP experience and qualification expertise in a GMP environment are assets. • Strong coordination skills, collaborative spirit, self-driven attitude, high level of learning agility are key attitudes • Eager to develop new methods and assess new analytical techniques. • High level of intrinsic motivation, excellent collaborative spirit and agility are key elements for our success. • Analyse and interpret complex situations, provide detailed directions for analytical approaches 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. 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 inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) 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 Job(link is external)Access Job Account(link is external)

Job ID 392705BR Apr 18, 2024 Switzerland About the Role Location: Basel, Switzerland Full time, permanent, onsite, #LI-Onsite Are you a curious, independent scientist? Do you know what is Radioligand therapy and how it can revolutionize cancer treatment? Come and join our team and together we can make a difference. The oncology research department in Biomedical Research, the innovation engine of Novartis, is recruiting a Senior Scientist with a strong background in cellular and molecular biology to join their Oncology Translational Research group in Basel, Switzerland. The successful candidate will carry out ground breaking research in the areas of translational/molecular oncology and radioisotope-based therapies in close collaboration with other leading research groups within Biomedical Research. You will be responsible for the generation of high-quality data to support the progress to the clinic of innovative radioligand research programs. By using a variety of molecular and cellular biology approaches the candidate will aim to decipher the cellular mechanisms underlying the activity of radioligand conjugates. Furthermore, you will contribute to the identification of molecular predictors of response and resistance to radioisotope-based therapies, as well as to exploring combination therapy opportunities. The ideal candidate will have a strong background in DNA damage response field and in vitro radiation biology. We seek an experienced, motivated and bold scientist wishing to continue a successful scientific career in a fast-paced drug discovery environment. Your responsibilities will include: • Independently design, perform and interpret in vitro experiments under the leadership of the Lab Head • Propose experimental alternatives, explore and introduce novel technologies and approaches. • Analyse and effectively report data, as well as presenting the data in different team meetings • Safely and effectively work with radionuclides • Critical reading of the literature and ability to apply it to the project. • Closely work with multiple teams across expertise groups within Oncology • Efficiently contribute to maintain a functional laboratory, technical equipment and tools Diversity & Inclusion / EEO 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: • MSc (or equivalent experience) in radiobiology, cellular biology, molecular biology or another relevant discipline. Please note that we do not require a PhD/Postdoctoral level candidate for this particular position. • At least, 5-7 years of biomedical research. Experience in radiobiology, DNA damage response and/or cell death mechanisms is highly desirable. • Proficiency and hands-on experience in applying a wide range of cellular and molecular biological methods (in particular: Immunofluorescence RNAi, qRT-PCR, cloning, cell culture, cell viability/death assays, transient/stable cell line generation, immunoblotting, ELISA, FACS, cellular co-cultures) • Experience using basic bioinformatics tools to support experimental design, data analysis and interpretation is considered a plus • Excellent presentation and communication skills in English (oral/written) • Used to successfully work within a highly productive and fast-paced environment • Highly collaborative and self-motivated team player, with critical scientific thinking • Excellent organizational skills Why Novartis: 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 employee 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.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 inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) 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 Job(link is external)Access Job Account(link is external)

Job ID 394253BR Apr 17, 2024 Switzerland About the Role Major accountabilities: Please enter specific details in the Additional Specifications Details field Key performance indicators: Please enter specific details in the Additional Specifications Details field Minimum Requirements: Work Experience: NA. Skills: NA. Languages : English. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division Biomedical Research Business Unit Pharma Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Job Type Full time Employment Type Early Talent (Fixed Term) Shift Work No Apply to Job(link is external)

About the Role Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide. The Biomedical Research unit is the innovation engine of Novartis. We collaborate across scientific and organizational boundaries, with a focus on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. In Global Discovery Chemistry (GDC) in Basel, Switzerland, we are at the core of Novartis’ purpose, designing and making new molecules for treating patients. We are looking for a highly motivated, passionate researcher with a strong scientific background in chemistry and a curious mind-set. Your responsibilities • Work highly collaboratively in a multidisciplinary project team to discover and develop novel therapies for high unmet medical needs. • Plan and execute chemical syntheses of novel drug molecules, including peptides, aided by in silico tools and facilitated by state-of the art synthetic methodologies. • Purify, isolate and characterize intermediates and final compounds at various scales (mgs to grams). • Support other team members by sharing your know-how and experience across your work environment. • Discuss and communicate scientific results at project/group meetings. • Maintain high levels of laboratory safety. Role Requirements What you will bring to the role • A Master’s degree with a focus on synthetic organic chemistry. • At least 3 years of drug discovery experience in industry with excellent theoretical and practical knowledge in synthetic organic chemistry. • Some experience in peptide chemistry, including the use of peptide synthesizers, would be an advantage. • A passion for cutting-edge chemistry experimentation in the lab. • A mind-set of curiosity, creativity, collaboration and openness to diverse thinking, with an enthusiasm to develop yourself and others. • The ability to work in a fast-paced team-oriented matrix environment. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external)

Job ID 394946BR Apr 16, 2024 Switzerland About the Role Novartis is an innovative medicines company. Every day, we work to reimagine medicine to improve and extend people’s lives so that patients, healthcare professionals and societies are empowered in the face of serious disease. Our medicines reach more than 250 million people worldwide. The Biomedical Research unit is the innovation engine of Novartis. We collaborate across scientific and organizational boundaries, with a focus on powerful new technologies that have the potential to help produce therapeutic breakthroughs for patients. In Global Discovery Chemistry (GDC) in Basel, Switzerland, we are at the core of Novartis’ purpose, designing and making new molecules for treating patients. We are looking for a highly motivated, passionate researcher with a strong scientific background in chemistry and a curious mind-set. Your responsibilities • Work highly collaboratively in a multidisciplinary project team to discover and develop novel therapies for high unmet medical needs. • Plan and execute chemical syntheses of novel drug molecules, including peptides, aided by in silico tools and facilitated by state-of the art synthetic methodologies. • Purify, isolate and characterize intermediates and final compounds at various scales (mgs to grams). • Support other team members by sharing your know-how and experience across your work environment. • Discuss and communicate scientific results at project/group meetings. • Maintain high levels of laboratory safety. 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 • A Master’s degree with a focus on synthetic organic chemistry. • At least 3 years of drug discovery experience in industry with excellent theoretical and practical knowledge in synthetic organic chemistry. • Some experience in peptide chemistry, including the use of peptide synthesizers, would be an advantage. • A passion for cutting-edge chemistry experimentation in the lab. • A mind-set of curiosity, creativity, collaboration and openness to diverse thinking, with an enthusiasm to develop yourself and others. • The ability to work in a fast-paced team-oriented matrix environment. Why Novartis? 766 million lives were touched by Novartis medicines in 2021, and while we’re proud of this, we know there is so much more we could do to help improve and extend people’s lives. We believe new insights, perspectives and ground-breaking solutions can be found at the intersection of medical science and digital innovation. That a diverse, equitable and inclusive environment inspires new ways of working. We believe our potential can thrive and grow in an unbossed culture underpinned by integrity, curiosity and flexibility. And we can reinvent what's possible, when we collaborate with courage to aggressively and ambitiously tackle the world’s toughest medical challenges. Because the greatest risk in life, is the risk of never trying! Imagine what you could do here at Novartis! Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division Biomedical Research Business Unit Global Discovery Chemistry Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Research & Development Job Type Full Time Employment Type Temporary Shift Work No Apply to Job(link is external)Access Job Account(link is external)

Job ID 394253BR Mar 18, 2024 Switzerland About the Role There is a unique opportunity for a Discovery Postdoctoral Fellow to explore the underlying biology of novel Radioligand Therapies (RLTs), including the effect of RLTs on the tumor and its stromal microenvironment. The Discovery Fellow will have the opportunity to conduct innovative, interdisciplinary research and publish their results in leading journals. You will be part of our Oncology, Pharmacology team in Basel, Switzerland working very closely with Oncology Data Sciences. RLT is a form of precision nuclear medicine which specifically directs radiation to target cells in the tumor. This cutting-edge technology has demonstrated remarkable promise for cancer patients, with two Novartis compounds- Pluvicto (177Lu-PSMA-617) and Lutathera (177Lu-DOTATATE) recently gaining approval in patients with mCRPC and GEP-NETs respectively. As a new and emerging modality there is still a lot to learn about how RLTs engage with the tumor and modulate its stromal microenvironment. Preferred start date: as soon as possible (negotiable) Duration: 36 to 48 months Location: Novartis Campus, Basel, Switzerland Key responsibilities As a Discovery Fellow, you will: • Actively design and shape the research project. • Design and implement in vivo studies with syngeneic tumor models. Carry out ex vivo analysis of tumors by flow cytometry using large lymphoid/myeloid panels, single cell RNA Seq, IHC/IF etc. • Implement reductionist in vitro assays of CAF and immune cell function. • Work closely with data sciences to inform research questions and experiments. • Collaborate with Novartis researchers and academic partners. • Present at lab meetings, internal seminars and international conferences. • Publish research findings in leading peer-reviewed journals. #LI-Onsite #PDX 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: • PhD in Oncology, Molecular and Cellular Biology or related subject area (PhD students in the last year of their thesis work, are eligible to apply). • Hands on experience with in vivo tumor models and ex vivo analysis by flow cytometry. • Substantial experience with standard in vitro cell biology techniques (cell culture, lenti/retroviral infection, western blot, IF, qPCR etc). • Experience working with radioisotopes is highly desirable though not essential. • Strong publication record or other scientific achievements (i.e. awards, patents, grants) • Excellent analytical, communication, presentation and organizational skills • Passion for fundamental exploratory research and boundless curiosity How to apply Please submit your CV and cover letter by April 15 for consideration. Please make sure to discuss in the cover letter how this training program will help you fulfill your career goals. 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 diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division Biomedical Research Business Unit Oncology NIBR Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to Job(link is external)Access Job Account(link is external)

Job ID 379986BR Mar 22, 2024 Switzerland About the Role 13! The number of medicines Cardio Renal Metabolic (CRM) diseases currently in development at Novartis. Novartis is deeply committed to transforming the lives of people living with cardiovascular, renal and metabolic diseases. We believe that anyone living with these conditions has the right to a life free from pain, free from symptoms and free from disease - this is our vision for the future. Our mission is to reimagine medicine to extend and improve people’s lives – and our overall company strategy to achieve this is to Focus Novartis as a leading medicine company powered by data science and advanced therapy platforms The (Sr)* Global Program Clinical Head (GPCH) is the global clinical leader responsible for one or more clinical programs across indications, involving one or multiple compounds. As the leader of Global Clinical Team(s) (GCT), the GPCH is accountable for the design, implementation, and execution of a clinical development program(s) to support decision milestones, regulatory requirements, market access and owns the risk benefit-assessment for the program(s). The GCPH contributes to the disease area strategy. Your responsibilities include, but are not limited to: • Leading the GCT and representing Clinical Development on the Global Program Team (GPT) • Leading the creation of clinical components of key documents (e.g., Clinical Trial Protocols (CTPs), Investigator’s Brochures, Clinical Study Reports (CSRs), regulatory documents including maintenance of product licenses, registration dossiers, value dossiers, pharmaco-economic dossiers) with high quality and consistency with Integrated Development Plan (IDP) and Target Product Profile (TPP). Supports registration, market access, commercialization, and maintenance of product licenses (e.g., Core Data Sheet, Periodic Safety Update Report, clinical benefit-risk assessment for license renewals) for the compound(s) • May serve as the Clinical Development Representative on NIBR clinical/project teams to drive transition of pre-PoC (Proof of Concept) projects to Development Decision Point (DDP) • Post-DDP, leading the development and execution of the clinical strategy. Developing an endorsed (IDP) in line with the Target Product Profile (TPP) which is designed for successful global regulatory approval/market access for one or multiple treatment indications and/or multiple programs • Where applicable, supporting Business Development & Licensing (BD&L) activities Diversity & Inclusion / EEO We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. Role Requirements • MD or equivalent (preferred), PhD, or PharmD degree required, specialization in a subspecialty may be needed. Advanced clinical training/knowledge in disease area (renal) preferred with 6 years (MD or equivalent) • 10 years (PhD or PharmD) of involvement in clinical research or drug development in an industry environment spanning clinical activities in Phases I through III/IV, including submission dossiers • Advanced knowledge of assigned therapeutic area preferred, with the capability to innovate in clinical development study designs that provide relevant evidence to decision-makers, and to interpret, discuss and present clinical trial or section program level data • 5 years people management experience required; this may include management in a matrix environment • Thorough knowledge of Good Clinical Practice, clinical trial design, statistics, and regulatory/clinical development process • Experience with submissions and health authorities required. * Final job title (Senior GPCH, Band 2 / GPCH, Band 2) 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 consider Novartis? 236 million. That’s how many lives our products touched in 2022. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division 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 Job(link is external)Access Job Account(link is external)

Job ID 384547BR Mar 05, 2024 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! Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) 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 Job(link is external)Access Job Account(link is external)

Job ID 392731BR Feb 27, 2024 Switzerland About the Role 350 million! That is the estimated number of patients worldwide suffering of atopic dermatitis or psoriasis. Join Novartis to help find the right drugs to transform and improve patient's lives all around the world. You will provide medical and scientific leadership and expertise in a role that significantly impacts the entire Novartis Dermatology drug development pipeline. • Drive success of early global programs, develop and implement strategies to achieve clinical Proof of Concept or Proof of Mechanism to enable transition to further development • Drive success of late global programs when appropriate by developing and implementing strategies that lead to clinical pharmacology, design of mechanistic studies and profiling packages that meet regulatory requirements and support differentiated and competitive drug labeling • Provide scientific expert assessments and support for in-licensing opportunities, including due diligences Your responsibilities: Translational Medicine early clinical projects: In collaboration with your Translational Medicine Therapeutic Area Head or other Translational Medicine Experts • Develop high value decision-strategies for the Translational Medicine component of drug development projects from Research to clinical Proof of Concept or Proof of Mechanism in a single or multiple indications, including Parallel Indication Expansion-Proof of Concepts - Represent TM and lead global project teams through First in Human and Proof of Concept phase to drive strategy that enables development - In collaboration with research scientists, contribute to the proposal of new targets or indications for existing compounds; identify, develop, and implement strategy for preclinical support of clinical program-related scientific objectives. This includes assessment of medical need, proposal of clinical development pathways, and review of preclinical data for clinical implications, and other relevant activities - 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. - Responsible for clinical portions of the Integrated Development Plan, including the Clinical Development Plan and Clinical Pharmacology Plan • Accountable for compound and disease related biomarker strategies, working closely with Biomarker Experts in implementation • 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 • Provide medical and scientific leadership and expertise to all line functions on the study team • Leadership - Lead study-specific teams/ clinical trial teams - Represent TM or lead BR project teams • Represent clinical Translational Medicine aspects to Health Authorities and other stakeholders (e.g. payers, patient advocacy groups) • Represent clinical Translational Medicine in reviews of external opportunities • Oversee publication and external presentation of study results • Innovation: Champion and drive new clinical compound characterization opportunities and profiling approaches • Contribute to initiatives that drive innovation, quality, and efficiency across Translational Medicine Translational Medicine late-stage clinical projects: In collaboration with your Translational Medicine Disease Area Head: • Drive analysis of studies and present results to relevant decision boards • Communicate clinical team matters to Global Project Teams, relevant Novartis BioMedical Research and Global Development boards, and other Novartis Boards as required. • Evaluate clinical centers and foster communication with crucial collaborating investigators, regulatory authorities, and other stakeholders • Provide support for dose selection, design and other clinical pharmacology matters throughout the development cycle • Responsible for content and authoring of documents needed for submission documents with Translational Medicine input (CO, SCE, SCS, SCP, SBP) of NDAs, sNDAs, MAAs, BLAs from regulatory submission through drug registration, including advisory committee and scientific advice group meetings Key Performance Indicators: • Delivery of proposed Development Candidates, Integrated Development Plan Approval and Development transition point milestones, and early clinical study results, according to timelines • Team leadership skills that create high performing teams and drive efficient conduct of innovative, interpretable clinical results • Strong adherence to and modeling of Novartis values and behaviors • Quality of contribution to disease area strategy discussions and contribution to Clinical Pharmacology plans / Profiling strategy discussions and external collaborations Matrix people responsibility per project: 5-8 cross-functional members from within 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 First in Human, Proof of Concept, and driving the program after Proof of Concept by delivering key Profiling data to support regulatory submissions • Recognized Expert in field, drives project team clinical strategy. Works globally across Novartis 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’ll bring to the role: • Medical Degree and additional PhD/post-doctoral equivalent immunology research • Specialized further training (board certification) and / or clinical research experience in dermatology / immunology preferred • Advanced / business-level / fluent English (oral and written) • Recognized for medical expertise: demonstrated excellence and clinical / patient expertise in dermatology / immunology • Recognized for scientific expertise: respected by colleagues internally and externally, you’ve made significant contributions to your field and created / established new concepts; record of 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 leading the medical relationship with Sponsors; from a relevant academic medical center with PI & co-PI clinical trial experience. You are used to working independently and within teams including scientists and non-scientists on study planning and execution, demonstrating competence in a broad range of project and more strategic planning skills • Excellent written and oral communication/presentation skills, used to distilling and effectively conveying significant messages to different audiences Your behavioral 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 • Innovation: a curious mind and a natural instinct to seek out new clinical discovery opportunities and clinical study approaches • Results-driven self-starter and decision taker; good planning, prioritization, problem solving and organizational skills; strong cooperative team player, flexible in a changing environment; Resilient, energetic and enthusiastic; responding constructively to challenging new ideas and input This position is written for Director - we can hire Executive Director for those with significant Pharma careers, or Associate Director if you have limited clinical study experience or a less established scientific record but have already demonstrated impactful new thinking and innovative clinical & scientific approaches within your career. 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-Scientist Discovery & Profiling group drives innovative and cutting–edge science from Discovery to the market through the selection, profiling and effective global development of successful medicines. The group closes the gap between preclinical research and clinical development and integrates clinical science into the discovery and preclinical development phase. Our Translational Medicine concepts are driven by medical needs of the patient and the concept of personalized medicine, tailoring the drug, its dose and dosing regimen in such way to the patient that the clinical response is optimal in terms of 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 together with a project team from researcher, biomarkers, biostatistics, modeling and simulation, toxicology, technical experts and the clinical trial teams. Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) 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 Job(link is external)Access Job Account(link is external)

Job ID 393805BR Mar 14, 2024 Switzerland About the Role Location: Basel, Switzerland #LI-Hybrid Getting people the medicines they need presents a series of complex challenges that can only be overcome with curiosity, determination and the support of a strong, united team. Join us and you can be part of that team. As the Head Legal, Secretary Pension Fund Board of Trustees, you will carry out the statutory activities of the Pension Fund in accordance with legal and regulatory requirements including accounting, controlling, financial and statutory reporting and information Your key responsibilities: • Support plan changes and maintenance of pension scheme in line with personnel policy of the Company • Ensure compliance with all legal and Board-issued requirements • Ensure safe and efficient asset management as a member of the Investment Committee • Analyse and follow-up on legal developments and ensure impeccable application within the Pension Funds • Continuously train and advise the Pension Funds’ associates, members of the Boards of Trustees, company representatives and insured members and pensioners according to their respective needs • Organize and moderate meetings and workshops of the Boards of Trustees • Represent the Pension Funds in legal matters and maintain contact to authorities • Act as Secretary and member of the Novartis Pension Board 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: • Several years of practical experience as a lawyer, preferably in the field of occupational pensions or another branch of social insurance • Degree in law (BLaw, MLaw, lic. iur.) and/or other further legal training with a comparable focus • Proficiency in German and English (written and spoken) • Efficient, precise and structured way of working with a flair for figures • Collaborative and solution-orientated personality with a strong service mentality • Knowledge in the field of investment management paired with strong negotiating skills and experience and joy in giving trainings and facilitating workshops 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 diversity.inclusion_ch@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division People & Organization Business Unit P&O CoE Total Rewards Location Switzerland Site Basel Company / Legal Entity Pensionskasse Novartis Functional Area Human Resources Job Type Part Time Part Time percentage 80 Employment Type Regular Shift Work No Apply to Job(link is external)Access Job Account(link is external)

Job ID 393658BR Mar 06, 2024 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 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 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: • 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! 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! Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division Development Business Unit GCO GDD Location Switzerland Site Basel Company / Legal Entity Novartis Pharma AG Alternative Location 1 United Kingdom Alternative Location 2 Ireland Alternative Location 3 India Functional Area Research & Development Job Type Full Time Employment Type Regular Shift Work No Apply to Job(link is external)Access Job Account(link is external)

About the Role This position is available in Switzerland or US. BioMedical Research (BR) is the global pharmaceutical research organization of Novartis. With approximately 6,000 scientists and physicians around the world, our research is focused on discovering innovative new drugs that will change the practice of medicine. We have an open and entrepreneurial culture, encouraging collaboration to make effective therapies. At BR, our mission is to discover innovative medicines that treat disease and human health. To do that, our scientists need cutting-edge, state-of-the-art computing systems. With Research Informatics (RX), BR is making a strategic investment into informatics capabilities and is positioning itself to deliver the systems and services that are critical to the future of drug discovery. About the department & role purpose The Scientific Data and Products (SDP) group in RX builds and applies excellence in product and data management to continuously improve the impact and value of software and data to NIBR. We deliver intuitive, intentional, and integrated software solutions that create a frictionless user experience. As an Associate Director Product Growth Manager you flexibly engage to lead diverse active development initiatives in the Product matrix within the context of an existing Product or software application, in leading and coordinating activities across multiple Products, or in creating a new Product or software application. You ensure the initiatives you lead contribute to an intentional, integrated, and capability-based product architecture and continuously increase the value defined by the strategic mandates of our Product Lines to deliver significant impact to drug discovery. Key Responsibilities: You use your knowledge of science and drug discovery as well as your understanding of the RX Product ecosystem and our strategic context to evaluate or invent new solutions across business domains. To do this, you co-lead medium to large matrixed, cross-functional teams consisting of software, data and infrastructure engineers, business analysts, designers, and user supporters and trainers, or you coordinate execution across several existing cross-functional teams. Specifically: • You provide strategic context and focus to the teams, facilitate prioritization, and cultivate good team-based decision-making practice. • You actively and transparently manage, and communicate to, all key business leaders to co-create visions and roadmaps for the initiatives you lead, and you define how we measure their success and value delivery. • You shape your teams’ culture and processes for success by exemplifying excellence in leadership and product management. • You ensure adherence to security, quality, and regulatory standards and policies, including GxP compliance if applicable. Role Requirements Essential Requirements: • Domain expertise in a core drug discovery scientific field such as biology, chemistry, computational sciences or core supporting field, with a broad knowledge of drug discovery • Team leadership experience in an agile environment within a complex enterprise organisation • Good experience in scientific software product management in a sophisticated matrix environment • Creativity in identifying, encouraging, and accelerating innovative solutions, including in GxP regulated environments if applicable • Ability to effect change, manage conflict, and create consent through direct and indirect influence • Proficiency in English (written & oral) 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 Why consider Novartis? 769 million. That’s how many lives our products touched in 2019. And while we’re proud of that fact, in this world of digital and technological transformation, we must also ask ourselves this: how can we continue to improve and extend even more people’s lives? We believe the answers are found when curious, courageous and collaborative people like you are brought together in an inspiring environment. Where you’re given opportunities to explore the power of digital and data. Where you’re empowered to risk failure by taking smart risks, and where you’re surrounded by people who share your determination to tackle the world’s toughest medical challenges. Imagine what you could do at Novartis! Commitment to Diversity & Inclusion: Novartis embraces diversity, equal opportunity and inclusion. We are committed to building diverse teams, representative of the patients and communities we serve, and we strive to create an inclusive workplace that cultivates bold innovation through collaboration, and empowers our people to unleash their full potential. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to learn more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external)

Job ID 393600BR Mar 21, 2024 Switzerland About the Role Location: Basel, Switzerland Fulltime, Onsite, #LI-onsite Novartis' Biomedical Research division is our Innovation engine. We have bold objectives to transform the lives of millions of people living with diseases and conditions and unmet medical needs. Applications are invited for a Senior Research Scientist to carry out cutting-edge oncology drug discovery pharmacology research. We seek an experienced, motivated and ambitious individual with a passion for in vivo oncology research. You will join the Radioligand Therapy (RLT) team to develop and validate novel targets in our world leading Oncology portfolio. The position is based in Basel, Switzerland. The ideal candidate should have a passion for working with rodents and a drive to perform in vivo oncology pharmacology studies including micro-surgeries, compound administration and preparation of samples for ex vivo analysis. Hands-on background performing small animal imaging modalities such as PET/SPECT/uCT or in cell biology techniques is a plus. The successful candidate will work collaboratively as an integral part of global projects and be an active member of lab and project teams. Responsibilities include but are not limited to: • Develop and characterize novel in vivo oncology models • Perform efficacy studies with cutting edge radioligand therapies • Perform biodistribution studies and metabolites analysis • Perform pre-clinical imaging studies including PET/SPECT/uCT • Perform and/or support colleagues with various in vitro and ex vivo activities (e.g. cell culture, flow cytometry, IHC, immunofluorescence, PCR, Western blotting) 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: • Masters degree in pharmacology, cell biology, medical physics, bioengineering, biotechnology or related field or Bachelors degree with equivalent experience. Please note that for this position we do not require a PhD qualified candidate at this time. • Practical work experience in biomedical research from an industry or academic laboratory • Experience in performing animal studies (animal handling, drug application, sampling, animal welfare regulations, small laboratory animal surgery) • Self-motivated, proactive, and able to work independently Desirable requirements • Knowledge and experience of standard cell biology techniques is desirable: cell culture, IHC, immunofluorescence, flow cytometry, quantitative real-time PCR, transfection, western blotting, etc., • Highly collaborative team player that enjoys working across multi-disciplinary teams • Excellent organizational and communication skills • Knowledge of cancer biology 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 inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Join our Novartis Network: If this role is not suitable to your experience or career goals but you wish to stay connected to hear more about Novartis and our career opportunities, join the Novartis Network here: https://talentnetwork.novartis.com/network *Please note that restrictions on flexible working may apply and will be discussed at interview stage if applicable Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) 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 Job(link is external)Access Job Account(link is external)

Job ID REQ-10000309 Apr 17, 2024 Switzerland About the Role Major Accountabilities Own the Training Curriculum for own Job Profile Lead or contribute to equipment, utility, facility improvement projects (e.g. energy efficiency, productivity, environmental compliance, maintenance) Get permits for maintenance / calibration / projects -Develop Project Cost Estimation And Value Improvement Review Identify technical solutions -Prepare project procurement plan, perform project tendering and procurement Perform project HSE management And execute project safety stops/reviews Maintenance Coordinator Ensures equipment operates to required HSE, Quality, Environmental and Reliability standards Support internal and external audits Implement GOPs Manage maintenance improvement projects and initiatives (local or corporate) Establish maintenance And calibration plan content Enter master data into CMMS (e.g. confirmation and technician time allocations) Coordinate maintenance / calibration activities Plan resources for maintenance / calibration Allocate work for maintenance / calibration to technicians Identify key compliance issues and suggest suitable solutions and determine, together with expert units involved, measures to eliminate safety and GMP problems in the technical sector Maintain documentation and preserve know-how regarding engineering procedures / sequences Organize maintenance to ensure conservation of value, availability of the machines assigned Act as contact engineer for the machines assigned, ensure appropriate management and development of the subordinate employees Manage ad hoc projects Compile regulations and principles Manage and execute project in alignment with key local and global stakeholders Execute projects according life cycle costs and project schedules Ensure state of the art technical solutions according compliance standards and HSE regulations Ensure projects on site are developed through their various stages of scope, definition, approval and implementation Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt Key performance indicators: Reliability of technical solutions and operability (breakdowns, availability, simplicity of maintenance and/or project execution) Out of Specification (OOS), Out of Expectations (OOE), product deviations or rejects related to equipment in area of responsibility Cost effective technical solutions in area of responsibility Highest safety standard implemented during projects and operations, no critical findings in HSE audits, no LTI and SIF Equipment availability Minimum Requirements: Work Experience: GMP environment. Chemical plant. Collaborating across boundaries. Functional Breadth. Skills: Emerson DeltaV system. Managing business continuity. Managing performance improvement. Managing and controlling costs. Languages : German. English. Why Novartis? Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Benefits and Rewards: Competitive salary, Annual bonus, Flexible working schedule, tailored to your needs, Unlimited learning and development opportunities. Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards 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 diversity.inclusion_ch@novartis.com 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: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division Operations Business Unit Pharmaceuticals Location Switzerland Site Muttenz (with Canteen) Company / Legal Entity C049 (FCRS = CH028) Novartis Pharma Schweizerhalle AG Functional Area Technical Operations Job Type Full time Employment Type CDI Shift Work No Apply to Job(link is external)

About the Role 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. This role will help get our Cell & Gene Therapy product to reach our patient worldwide. Cell & Gene Therapy at Novartis is a very dynamic and innovative environment, focus on delivering bring therapy to the patient. Your key responsibilities: Your responsibilities include, but are not limited to: • Perform Bio-Analytical testing such as Flow, ELISA, cell count, cell viability, residual bead assessment, qPCR, Potency, in collaboration with experienced team members, if necessary • Perform all testing and activities compliantly following appropriate SOPs and procedures and maintain controls, reagents and reference standards to support testing • Work on shifts covering daytime / evening and one or both weekend days • Knowledge of LabWare LIMS and/or other QC data systems • Ensure all activities in compliance with cGxP, incl. data integrity Role Requirements • Sample storage and management • Knowledge of LabWare LIMS and/or other QC data systems Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external)

About the Role 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. This role will help get our Cell & Gene Therapy product to reach our patient worldwide. Cell & Gene Therapy at Novartis is a very dynamic and innovative environment, focus on delivering bring therapy to the patient. Your key responsibilities: Your responsibilities include, but are not limited to: • Perform Bio-Analytical testing such as Flow, ELISA, cell count, cell viability, residual bead assessment, qPCR, Potency, in collaboration with experienced team members, if necessary • Perform all testing and activities compliantly following appropriate SOPs and procedures and maintain controls, reagents and reference standards to support testing • Work on shifts covering daytime / evening and one or both weekend days • Knowledge of LabWare LIMS and/or other QC data systems • Ensure all activities in compliance with cGxP, incl. data integrity Role Requirements • Sample storage and management • Knowledge of LabWare LIMS and/or other QC data systems Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external)

Job ID REQ-10001596 Apr 18, 2024 Switzerland About the Role Accountabilities: 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. 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 diversity.inclusion_ch@novartis.com 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/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division Operations Business Unit Pharmaceuticals Location Switzerland Site Stein Aargau Company / Legal Entity C046 (FCRS = CH028) Novartis Pharma Stein AG Functional Area Technical Operations Job Type Full time Employment Type Befristet (Befristet) Shift Work No Apply to Job(link is external)

Job ID 392875BR Feb 28, 2024 Switzerland About the Role Unser Novartis Seriles-Werk in Stein ist einer der wichtigsten Standorte für innovative, hochqualitative, sterile Medikamente, die wir jeden Tag produzieren, verpacken und an unsere Patienten in über 150 Ländern verschicken. Wir suchen nach zwei motivierten Postgraduates / Postdocs, die gerne unsere Manufacturing Unit in der Galenik unterstützen und wertvolle Einblicke in die pharmazeutische Industrie erhalten möchte. Präferiertes Startdatum: sobald wie möglich, z.B. 1. Mai 2024 Dauer: 1 Jahr Ihre Aufgaben werden beinhalten: • Trouble Shooting und Support für die Herstellung • Bearbeitung von Deviations, Actions & CAPAs im Ansatzbereich • Erstellung und Überarbeitung von bereichsspezifischer SOP’s • Unterstützung bei Qualifizierungstätigkeiten (z.B. thermische Requalifizierung, Neuanlagen) • Reviewed und genehmigt Herstellvorschriften in MES PAS-X, arbeitet Exceptions in MES ab und prüft die Herstelldokumentation #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 Was Sie mitbringen: • Bachelor, Master oder Doktor-Abschluss in einem naturwissenschaftlichen Studiengang, z.B. Biotechnologie, Pharmazeutische Technologie, Pharmazie, Chemie oder ähnlich (abgeschlossen in den letzten ca. 12 Monaten) • Sprachen: sehr gute Deutsch- und Englischkenntnisse in Wort und Schrift • Sehr gute MS Office Kenntnisse • Hohes Qualitätsbewusstsein • Offene und aufgeschlossene Persönlichkeit • Selbstständiges Arbeiten, Engagement und hohe Einsatzbereitschaft Bitte fügen Sie ein Motivationsschreiben bei, in welchem Sie Ihre Motivation für diese Position erklären und uns informieren, ab wann Sie verfügbar sind. Vielen Dank. Warum Novartis? Unser Vorsatz ist es, die Medizin neu zu gestalten, um Menschenleben zu verbessern und zu verlängern. Unsere Vision ist es, das wertvollste und vertrauenswürdigste Pharmaunternehmen der Welt zu werden. Wie wir das erreichen werden? Mit unseren Mitarbeitern. Es sind unsere Mitarbeiter, die uns tagtäglich dazu antreiben, unsere Ziele zu erreichen. Werden Sie Teil dieser Mission und dieses großartigen Teams! Erfahren Sie hier mehr: https://www.novartis.com/about/strategy/people-and-culture Was wir bieten: Alle Informationen finden Sie in unserem Novartis Life Handbook (Englisch): https://www.novartis.com/careers/benefits-rewards Barrierefreiheit und Unterstützung: Wenn Sie aufgrund einer Erkrankung oder Behinderung spezielle Unterstützung während des Rekrutierungsprozesses brauchen und/oder deswegen detailliertere Informationen über die wesentlichen Funktionen einer Stelle benötigen, senden Sie bitte eine E-Mail an diversity.inclusion_ch@novartis.com und teilen Sie uns die Art Ihres Anliegens und Ihre Kontaktinformationen mit. Bitte vergessen Sie nicht, dabei die Referenznummer der Stellenausschreibung anzugeben. Treten Sie unserem Novartis Netzwerk bei: Wenn diese Position nicht zu Ihrer Erfahrung oder Ihren Karrierezielen passt, Sie aber dennoch mit uns in Kontakt bleiben möchten, um mehr über Novartis und unsere Karrieremöglichkeiten zu erfahren, dann treten Sie hier dem Novartis Netzwerk bei: https://talentnetwork.novartis.com/network Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division Operations Business Unit LARGE MOLECULES Location Switzerland Site Stein (Säckingen) Company / Legal Entity Novartis Pharma AG Functional Area Interns/Students on Novartis Payroll Job Type Full Time Employment Type Internship Shift Work No Apply to Job(link is external)Access Job Account(link is external)

Job ID 394897BR Apr 11, 2024 Switzerland About the Role Wir suchen einen QC Specialist I in unserem Laboratory Support & New Technologies (LSNT) Team. Das LSNT Team ist ein zentralisiertes Team innerhalb der Quality Control Organisation Stein LM, welches die Standardisierung und Harmonisierung über alle QC / AS&T Labore und darüber hinaus ermöglicht. Das Team zeichnet sich durch eine grosse Diversität aus und liefert einen wertvollen Beitrag bei laborübergreifenden Digitalisierungs- und Automatisierungsprojekten. In der Rolle als QC Specialist I betreust du die periodischen Re-Qualifizierungen, Kalibrierungen und Wartungen von unterschiedlichen Laborgeräten (u.a. HPLC, CE, Waagen). Du unterstützt zudem qualifizierungsrelevante Aktivitäten, wie bspw. die Re-Evaluierung von Kategorie C Geräten, Durchführung von User Reviews oder technischen Audit Trail Reviews. Desweiteren unterstützt du das Labor bei Geräteproblemen und führst technische Abweichungen eigenständig durch. Die Position zeichnet sich durch ein vielfältiges Aufgabenfeld aus und ermöglicht es dir, sowohl technische als auch prozessbezogene Aspekte der Qualitätskontrolle zu betreuen. In deiner Funktion arbeitest du eng mit den Laboren zusammen und trägst massgeblich zur weiteren Harmonisierung der physisch / chemischen Labore bei Stein Steriles bei. Key Responsibilities: Betreuung und Durchführung von periodischen Re-Qualifizierungen, Kalibrierungen und Wartungen von Laborgeräten in einem GxP-regulierten Umfeld. Unterstützung qualifizierungsrelevanter Aktivitäten: Re-Evaluierung von Kategorie C Geräten, User Reviews und technische Audit Trails Reviews. Unterstützung bei Geräteproblemen und technischen Abweichungen. Durchführung von Änderungskontrollen und Qualifizierungen von Kategorie B Geräten. 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 Fundierte technische und wissenschaftliche Kenntnisse im Bereich der pharmazeutischen/chemischen Analytik/QC/Äquivalent . Arbeitserfahrung in einer Laborumgebung in der pharmazeutischen Industrie. Fliessend Deutsch, Englischkenntnisse Industrie GxP Standards und Prozesse Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network(link is external) Division 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 Job(link is external)Access Job Account(link is external)