Novartis AG

Job ID REQ-10067434 Apr 09, 2026 Switzerland Summary Linienführer:in Primärverpackung - Feste Darreichungsformen Für unser Team in der Primärverpackung fester Darreichungsformen suchen wir per sofort eine:n motivierte:n und erfahrene:n Linienführer:in mit fundierten GMP-Kenntnissen, ausgeprägtem technischem Verständnis und Teamgeist. In dieser Funktion sind Sie verantwortlich für die termingerechte Ausführung der Ihnen zugewiesenen Herstellungs- und Verpackungsaufgaben gemäß Produktionsplan unter Einhaltung aller GMP-, Sicherheits- und Umweltrichtlinien. About the Role Hauptaufgaben Maschinelles Verpacken von Arzneimitteln (Flaschen und Blister) an modernen, komplexen Verpackungsanlage Führen, Einteilen und Unterstützen des Anlagenteams der zugewiesenen Produktionslinie Umrüsten/ Einrichten und Anfahre/Betreiben der Produktionsanlagen Verantwortung für die Anlagenreinigung und Desinfektion Durchführung von In-Process-Control (IPC)-Kontrollen Auftragsvorbereitung in Zusammenarbeit mit Planung, Lager und Prozessexpert:innen Beheben kleiner technischer Störungen; Unterstützung bei Qualifizierungs- und Instandhaltungsarbeiten nach Bedarf Einarbeitung neuer Mitarbeitender im Bereich Korrekte, vollständige und nachvollziehbare Dokumentation der Tätigkeiten auf Papier und in der elektronischen Chargendokumentation (z. B. SAP) gemäß GMP Fachansprechpartner:in für die zugewiesenen Anlagen und Prozesse bei Audits und Inspektionen Sicherstellung und Durchsetzung von GMP- und HSE-Vorgaben Mitwirkung am Housekeeping (Ordnung, Sauberkeit, 5S) im Produktionsbereich Kontinuierliche Verbesserung: Identifikation von Schwachstellen und Vorschlag von Maßnahmen (Organisation, Prozess, Sicherheit, Hygiene) Teilnahme an allen funktionsrelevanten Schulungen und Sicherstellung des geforderten Trainingsstandes Bereitschaft zu Mehrarbeit bzw. Schichtarbeit (Früh- und Spätschicht), sofern erforderlich Zusammenarbeit mit anderen Einheiten und Einsatz in angrenzenden Bereichen bei Bedarf (z. B. weitere Primärverpackungslinien, Lager, Sekundärverpackung, Manuelle Handverpackung) Erforderliche Fähigkeiten Abgeschlossene Ausbildung im Bereich Chemie / Pharma oder Technik Berufserfahrung als Linienführer:in/Linienleiter:in im GMP-regulierten Umfeld, idealerweise in der Verpackung pharmazeutischer Produkte (Flaschen und Blister)Ausgeprägte technische Kompetenz mit Erfahrung im Einrichten, Bedienen und Störungsbeheben an automatisierten Produktionsanlagen Hohes Pflicht- und Qualitätsbewusstsein; sorgfältige Dokumentations- und Arbeitsweise sowie Ordnung und Sauberkeit am Arbeitsplatz Konstruktiv, lösungsorientiert, verantwortungsbewusst; tiefes Verständnis für Qualität und Compliance Hohe Selbstmotivation und schnelle Auffassungsgabe zur Einarbeitung in neue Tätigkeiten Erfahrung in der Führung kleiner Teams und in der Mitarbeitendenausbildung von Vorteil Gute IT- sowie MS-Office-Kenntnisse (z. B. Erstellung einfacher Arbeits- oder Bedienungsanweisungen) Fundierte Kenntnisse im GMP-Umfeld und in hygienekritischen Bereichen Organisationstalent und Durchsetzungsvermögen Sehr gute Deutschkenntnisse in Wort und Schrift; Englischkenntnisse von Vorteil 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: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Development Business Unit Development Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Temporary (Fixed Term) Shift Work No Play Play 00:00 Play Seek 10 seconds backwards Seek 10 seconds forward 00:00 / 01:54 Mute Click to volume controlUse the arrows to control the volume Settings Turn on Picture in picture Show Full screen Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Research & Development Development Switzerland Job ID REQ-10067434 Process Technician - Supply Management Apply to Job (link is external)

Summary Location: Basel Switzerland or East Hanover NJ, or Cambridge MA US. This role will follow a hybrid working model. If based in the US please apply to REQ-10075152 LI-#hybrid The Novartis Strategy & Growth, Therapeutic Area Strategy team for Neuroscience is seeking a new Therapeutic Area Strategy Director who will support the creation and update of a holistic TA strategy; provide early-phase commercial insights to project teams; guide TA-specific internal pipeline development and external licensing / acquisitions opportunities; and support integrated enterprise alignment across Biomedical Research (BR), Development, Strategy & Growth (S&G), and the Commercial US and International units. About the Role Key Responsibilities: Brings external benchmarking, analysis and insights, and judgement to support the TA Strategy Head in developing a holistic Novartis TA strategy that achieves sustainable growth in short, mid and long-term. Brings both understanding of the pharmaceutical industry and the core Therapeutic Areas (TA) and Disease area of Neuroscience to derive insightful and differentiating competitive advantages over our peers. Provides key commercial insights to the R&D project teams, particularly for early phase programs. To do this effectively, in-market experience in the US is critical. Analyses reports and publications to extract key messages, including building product forecasts. Supports development and delivery of TA-specific strategic external insights to support identification of growth opportunities, emerging competitive challenges and support creation of a third-party view around key strategic levers, and commissions targeted primary research. Essential Requirements: Bachelor's degree required. Advanced degree (PhD, MD or other advanced University degree) and / or equivalent experience in life science/healthcare; MBA or consulting or equivalent experience highly preferred. In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) in Neuroscience. Highly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and external Substantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs). At least 5-7 years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary research Experience of strategy development and asset shaping early in lifecycle (any functional perspective) Recent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systems 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Job ID REQ-10075151 Apr 14, 2026 Switzerland Summary Location: Basel Switzerland or East Hanover NJ, or Cambridge MA US. This role will follow a hybrid working model. If based in the US please apply to REQ-10075152 LI-#hybrid The Novartis Strategy & Growth, Therapeutic Area Strategy team for Neuroscience is seeking a new Therapeutic Area Strategy Director who will support the creation and update of a holistic TA strategy; provide early-phase commercial insights to project teams; guide TA-specific internal pipeline development and external licensing / acquisitions opportunities; and support integrated enterprise alignment across Biomedical Research (BR), Development, Strategy & Growth (S&G), and the Commercial US and International units. About the Role Key Responsibilities: Brings external benchmarking, analysis and insights, and judgement to support the TA Strategy Head in developing a holistic Novartis TA strategy that achieves sustainable growth in short, mid and long-term. Brings both understanding of the pharmaceutical industry and the core Therapeutic Areas (TA) and Disease area of Neuroscience to derive insightful and differentiating competitive advantages over our peers. Provides key commercial insights to the R&D project teams, particularly for early phase programs. To do this effectively, in-market experience in the US is critical. Analyses reports and publications to extract key messages, including building product forecasts. Supports development and delivery of TA-specific strategic external insights to support identification of growth opportunities, emerging competitive challenges and support creation of a third-party view around key strategic levers, and commissions targeted primary research. Essential Requirements: Bachelor's degree required. Advanced degree (PhD, MD or other advanced University degree) and / or equivalent experience in life science/healthcare; MBA or consulting or equivalent experience highly preferred. In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) in Neuroscience. Highly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and external Substantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs). At least 5-7 years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary research Experience of strategy development and asset shaping early in lifecycle (any functional perspective) Recent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systems 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 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. 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: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Strategy & Growth Business Unit General Management Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area BD&L & Strategic Planning Job Type Full time Employment Type Regular Shift Work No Play Play 00:00 Play Seek 10 seconds backwards Seek 10 seconds forward 00:00 / 01:54 Mute Click to volume controlUse the arrows to control the volume Settings Turn on Picture in picture Show Full screen Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. BD&L & Strategic Planning Strategy & Growth Switzerland Job ID REQ-10075151 Therapeutic Area Strategy Director, Neuroscience Apply to Job (link is external)

Job ID REQ-10076235 Apr 21, 2026 Switzerland Summary Location: Cambridge MA, East Hanover NJ, US or Basel Switzerland. This role will follow a hybrid working model. If based in US, please apply to REQ-10076159 LI-#hybrid The Novartis Strategy & Growth, Therapeutic Area Strategy team for Oncology & Hematology is seeking a new Executive Director, Therapeutic Area Strategy who will support the creation and update of a holistic TA strategy; provide early-phase commercial insights to project teams; guide TA-specific internal pipeline development and external licensing / acquisitions opportunities; and support integrated enterprise alignment across Biomedical Research (BR), Development, Strategy & Growth (S&G), and the Commercial US and International units. About the Role Key Responsibilities: Brings external benchmarking, analysis and insights, and judgement to support the TA Strategy Head in developing a holistic Novartis TA strategy that achieves sustainable growth in short, mid and long-term. Brings both understanding of the pharmaceutical industry and the core Therapeutic Areas (TA) and Disease area of Oncology & Hematology to derive insightful and differentiating competitive advantages over our peers. Provides key commercial insights to the R&D project teams, particularly for early phase programs. To do this effectively, in-market experience in the US is critical. Analyses reports and publications to extract key messages, including building product forecasts. Supports development and delivery of TA-specific strategic external insights to support identification of growth opportunities, emerging competitive challenges and support creation of a third-party view around key strategic levers, and commissions targeted primary research. Essential Requirements: Bachelor's degree required. Advanced degree (PhD, MD or other advanced University degree) and / or equivalent experience in life science/healthcare; MBA or consulting or equivalent experience highly preferred. In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) in Oncology and/or Hematology. Highly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and external Substantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs). 7-10 years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary research Experience of strategy development and asset shaping early in lifecycle (any functional perspective) Recent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systems 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 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. 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: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Strategy & Growth Business Unit Strategic Planning & BD&L Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area BD&L & Strategic Planning Job Type Full time Employment Type Regular Shift Work No Play Play 00:00 Play Seek 10 seconds backwards Seek 10 seconds forward 00:00 / 01:54 Mute Click to volume controlUse the arrows to control the volume Settings Turn on Picture in picture Show Full screen BD&L & Strategic Planning Strategy & Growth Switzerland Job ID REQ-10076235 Executive Director, Therapeutic Area Strategy, Oncology and Hematology Apply to Job (link is external)

Summary #LI-Hybrid Internal job title: Executive Director Location: Basel, Switzerland As the Head of Neurodegeneration within Translational Medicine, you will serve as a senior scientific and strategic leader responsible for shaping and delivering the translational strategy for neurodegenerative therapeutic programs. You will provide expert guidance bridging research, early clinical development, and biomarker/experimental medicine innovation to advance assets from discovery through proof-of-concept and into full development. In addition, you will lead or integrate global, cross-functional teams to design, implement, and execute cutting-edge translational strategies, and act as an influential thought partner in neurodegenerative disease biology, clinical development, and emerging therapeutic modalities. About the Role Key Responsibilities: Strategic Leadership & Scientific Direction Define and oversee the long-term translational strategy for the Neurodegeneration Pillar, ensuring scientific excellence and alignment with broader BR and TM organizational priorities. Serve as a senior advisor and thought leader within neurodegeneration disorders, leveraging deep specialty expertise to inform program design, biomarker strategy, and patient-relevant endpoints. Program & Portfolio Leadership Lead global translational teams across Phase I–IIa (“Discovery” through TDP), driving implementation of high‑quality development strategies in single or multiple neurodegeneration indications. Represent TM on global program teams (GPT) and decision boards, ensuring that neurodegeneration programs meet quality, regulatory, and differentiation objectives. Translational & Clinical Development Excellence Lead the design and execution of First‑in‑Human (FIH) and Phase IIa studies, working collaboratively with clinical, regulatory, biomarker, and profiling partners. Leads the creation of clinical components of key documents e.g., Clinical Trial Protocols (CTPs), Investigator’s Brochures, Clinical Study Reports (CSRs), regulatory documents etc. with high levels of quality and consistency Leadership of People, Culture, and Matrix Teams Serve as a culture champion, promoting empowerment, innovation, and collaboration across TM and broader BR organizations. Mentor and develop scientific talent across translational and clinical functions. External Impact & Partnerships Lead interactions with external stakeholders (e.g., regulatory authorities, key opinion leaders, data monitoring committees, advisory boards etc.) and internal NVS stakeholders Contribute to opportunity assessments and due diligence for neurodegeneration and adjacent therapeutic areas. Governance, Compliance & Documentation Essential Requirements: MD and PhD required with clinical subspecialty training in neurological diseases with deep expertise in neurodegeneration disorders A minimum of 10+ years of extensive experience in translational medicine, early clinical development, or experimental therapeutics. Demonstrated success leading complex global programs and cross-functional scientific teams. Proven ability to shape development strategies, execute early clinical studies, and influence regulatory/packages supporting differentiation. Experience working in pharmaceutical/biotech company strongly preferred. Desirable Requirements: Direct people management experience 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Linienführer:in Primärverpackung – Feste Darreichungsformen Für unser Team in der Primärverpackung fester Darreichungsformen suchen wir per sofort eine:n motivierte:n und erfahrene:n Linienführer:in mit fundierten GMP-Kenntnissen, ausgeprägtem technischem Verständnis und Teamgeist. In dieser Funktion sind Sie verantwortlich für die termingerechte Ausführung der Ihnen zugewiesenen Herstellungs- und Verpackungsaufgaben gemäß Produktionsplan unter Einhaltung aller GMP-, Sicherheits- und Umweltrichtlinien. About the Role Hauptaufgaben Maschinelles Verpacken von Arzneimitteln (Flaschen und Blister) an modernen, komplexen Verpackungsanlage Führen, Einteilen und Unterstützen des Anlagenteams der zugewiesenen Produktionslinie Umrüsten/ Einrichten und Anfahre/Betreiben der Produktionsanlagen Verantwortung für die Anlagenreinigung und Desinfektion Durchführung von In-Process-Control (IPC)-Kontrollen Auftragsvorbereitung in Zusammenarbeit mit Planung, Lager und Prozessexpert:innen Beheben kleiner technischer Störungen; Unterstützung bei Qualifizierungs- und Instandhaltungsarbeiten nach Bedarf Einarbeitung neuer Mitarbeitender im Bereich Korrekte, vollständige und nachvollziehbare Dokumentation der Tätigkeiten auf Papier und in der elektronischen Chargendokumentation (z. B. SAP) gemäß GMP Fachansprechpartner:in für die zugewiesenen Anlagen und Prozesse bei Audits und Inspektionen Sicherstellung und Durchsetzung von GMP- und HSE-Vorgaben Mitwirkung am Housekeeping (Ordnung, Sauberkeit, 5S) im Produktionsbereich Kontinuierliche Verbesserung: Identifikation von Schwachstellen und Vorschlag von Maßnahmen (Organisation, Prozess, Sicherheit, Hygiene) Teilnahme an allen funktionsrelevanten Schulungen und Sicherstellung des geforderten Trainingsstandes Bereitschaft zu Mehrarbeit bzw. Schichtarbeit (Früh- und Spätschicht), sofern erforderlich Zusammenarbeit mit anderen Einheiten und Einsatz in angrenzenden Bereichen bei Bedarf (z. B. weitere Primärverpackungslinien, Lager, Sekundärverpackung, Manuelle Handverpackung) Erforderliche Fähigkeiten Abgeschlossene Ausbildung im Bereich Chemie / Pharma oder Technik Berufserfahrung als Linienführer:in/Linienleiter:in im GMP-regulierten Umfeld, idealerweise in der Verpackung pharmazeutischer Produkte (Flaschen und Blister)Ausgeprägte technische Kompetenz mit Erfahrung im Einrichten, Bedienen und Störungsbeheben an automatisierten Produktionsanlagen Hohes Pflicht- und Qualitätsbewusstsein; sorgfältige Dokumentations- und Arbeitsweise sowie Ordnung und Sauberkeit am Arbeitsplatz Konstruktiv, lösungsorientiert, verantwortungsbewusst; tiefes Verständnis für Qualität und Compliance Hohe Selbstmotivation und schnelle Auffassungsgabe zur Einarbeitung in neue Tätigkeiten Erfahrung in der Führung kleiner Teams und in der Mitarbeitendenausbildung von Vorteil Gute IT- sowie MS-Office-Kenntnisse (z. B. Erstellung einfacher Arbeits- oder Bedienungsanweisungen) Fundierte Kenntnisse im GMP-Umfeld und in hygienekritischen Bereichen Organisationstalent und Durchsetzungsvermögen Sehr gute Deutschkenntnisse in Wort und Schrift; Englischkenntnisse von Vorteil 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Job ID REQ-10076205 May 07, 2026 Switzerland Summary #LI-Hybrid Internal job title: Director Location: Basel, Switzerland Translational Medicine Discovery & Profiling (TMDP) is a group of physicians and clinical researchers who drive innovative science from discovery to the patient through the selection, profiling, and early clinical development of medicines. Medical directors oversee phase 1 first-in-human (FiH) and phase 2 proof-of-concept (PoC) and dose range finding (DRF) studies in support for Phase 3 development. Medical directors in translational medicine are key and highly visible members of global cross-functional project teams that design and implement early research and discovery projects. Medical directors in translational medicine collaborate with colleagues in biology and chemistry to identify targets in diseases with significant unmet medical needs and provide input on likely clinical development pathways, design clinical development plans in collaboration with late phase development, draft clinical trial protocols and serve as medical leads for these trials. As a Medical Director in Translational Medicine Gastroenterology, you will report to the TM Head. About the Role Key Responsibilities: Lead global clinical trial teams through phase 1 and 2 development Draft the early clinical development plan Act as medical lead for early clinical studies Represent the team in relevant decision boards Serve a primary contact for internal and external key opinion leaders Oversee publication and internal/external presentation of clinical study results Work closely with biomarker experts in implementation Collaborate with research scientists to identify, develop and implement strategy for preclinical support of program related objectives Actively participate in Health Authority interactions Essential Requirements: Medical doctor with board certification in gastroenterology. Several years of clinical experience treating IBD (UC and CD) patients. Ability to learn fast and work independently Ability to lead multidisciplinary teams in a matrix organization. Excellent communication and presentation skills Desirable Requirements: Research experience (e.g., Ph.D.) is a plus but not a strict requirement Drug development experience as trial investigator or pharma experience are a plus but not strict requirements. Publications in the field of IBD are a plus but not a strict requirement 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 Benefits and Rewards: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Biomedical Research Business Unit Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Play Play 00:00 Play Seek 10 seconds backwards Seek 10 seconds forward 00:00 / 01:54 Mute Click to volume controlUse the arrows to control the volume Settings Turn on Picture in picture Show Full screen Research & Development Biomedical Research Switzerland Job ID REQ-10076205 Medical Director, Gastroenterology, Early Clinical Development Apply to Job (link is external)

Summary Location: Basel Switzerland or Cambridge, MA. This role will follow a hybrid working model. If based in the US, please apply to REQ-10076684 LI-#hybrid The Novartis Strategy & Growth Therapeutic Area Strategy team for Cardio, Renal, and Metabolic (CRM) is seeking a Strategy Director. This role will support the development and ongoing evolution of a holistic TA strategy, provide early-phase commercial insights to project teams, and guide TA-specific internal pipeline development as well as external licensing and acquisition opportunities. The role will also support integrated enterprise alignment across Biomedical Research (BR), Development, Strategy & Growth (S&G), and Commercial US and International teams. About the Role Key Responsibilities: Brings external benchmarking, analysis and insights, and judgement to support the TA Strategy Head in developing a holistic Novartis TA strategy that achieves sustainable growth in short, mid and long-term. Brings both understanding of the pharmaceutical industry and the core Therapeutic Areas (TA) and Disease area of CRM to derive insightful and differentiating competitive advantages over our peers. Provides key commercial insights to the R&D project teams, particularly for early phase programs. To do this effectively, in-market experience in the US is critical. Analyses reports and publications to extract key messages, including building product forecasts. Supports development and delivery of TA-specific strategic external insights to support identification of growth opportunities, emerging competitive challenges and support creation of a third-party view around key strategic levers, and commissions targeted primary research. Essential Requirements: Bachelor's degree required. Advanced degree (PhD, MD or other advanced University degree) and / or equivalent experience in life science/healthcare; MBA or consulting or equivalent experience highly preferred. In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) in CRM. Highly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and external Substantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs). At least 5-7 years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary research Experience of strategy development and asset shaping early in lifecycle (any functional perspective) Recent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systems 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Location: Cambridge MA, East Hanover NJ, US or Basel Switzerland. This role will follow a hybrid working model. If based in US, please apply to REQ-10076236 LI-#hybrid The Novartis Strategy & Growth, Therapeutic Area Strategy team for Immunology is seeking a new TA Strategy Director who will support the creation and update of TA strategy; provide early-phase commercial insights to project teams; guide TA-specific internal pipeline development and external licensing / acquisitions opportunities; and support integrated enterprise alignment across Biomedical Research (BR), Development, Strategy & Growth (S&G), and the Commercial US and International units. About the Role Key Responsibilities: Brings external benchmarking, analysis and insights, and judgment to support the TA Strategy Head in developing Immunology therapeutic area strategy Brings both understanding of the pharmaceutical industry and the Immunology to derive insightful and differentiating competitive advantages over our peers Provides key commercial insights to the R&D project teams, particularly for early phase programs. This includes creating product forecasts and assessing competitive landscape and portfolio strategic fit. Analyses reports and publications to extract key messages, including building product forecasts Supports development and delivery of TA-specific strategic external insights to support identification of growth opportunities, emerging competitive challenges and support creation of a third-party view around key strategic levers, and commissions targeted primary research Supports strategy and commercial analysis for business development activities Actively contribute to Global /Unit Strategic Planning process Essential Requirements: Bachelor's degree required. Advanced degree (PhD, MD or other advanced University degree) and / or equivalent experience in life science/healthcare; MBA or consulting or equivalent experience highly preferred. In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) in Immunology. Highly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and external Substantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs). At least 5-7 years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary research Experience of strategy development and asset shaping early in lifecycle (any functional perspective) Recent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systems 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Location: Cambridge MA, East Hanover NJ, US or Basel Switzerland. This role will follow a hybrid working model. If based in US, please apply to REQ-10076159 LI-#hybrid The Novartis Strategy & Growth, Therapeutic Area Strategy team for Oncology & Hematology is seeking a new Executive Director, Therapeutic Area Strategy who will support the creation and update of a holistic TA strategy; provide early-phase commercial insights to project teams; guide TA-specific internal pipeline development and external licensing / acquisitions opportunities; and support integrated enterprise alignment across Biomedical Research (BR), Development, Strategy & Growth (S&G), and the Commercial US and International units. About the Role Key Responsibilities: Brings external benchmarking, analysis and insights, and judgement to support the TA Strategy Head in developing a holistic Novartis TA strategy that achieves sustainable growth in short, mid and long-term. Brings both understanding of the pharmaceutical industry and the core Therapeutic Areas (TA) and Disease area of Oncology & Hematology to derive insightful and differentiating competitive advantages over our peers. Provides key commercial insights to the R&D project teams, particularly for early phase programs. To do this effectively, in-market experience in the US is critical. Analyses reports and publications to extract key messages, including building product forecasts. Supports development and delivery of TA-specific strategic external insights to support identification of growth opportunities, emerging competitive challenges and support creation of a third-party view around key strategic levers, and commissions targeted primary research. Essential Requirements: Bachelor's degree required. Advanced degree (PhD, MD or other advanced University degree) and / or equivalent experience in life science/healthcare; MBA or consulting or equivalent experience highly preferred. In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) in Oncology and/or Hematology. Highly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and external Substantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs). 7-10 years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary research Experience of strategy development and asset shaping early in lifecycle (any functional perspective) Recent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systems 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Location: Basel Switzerland or Cambridge MA, East Hanover NJ, US. This role will follow a hybrid working model. If based in the US, please apply to REQ-10074642 LI-#hybrid The Novartis Strategy & Growth, Therapeutic Area Strategy team for Oncology is seeking a new Therapeutic Area Strategy Director, Oncology & Hematology who will support the creation and update of a holistic TA strategy; provide early-phase commercial insights to project teams; guide TA-specific internal pipeline development and external licensing / acquisitions opportunities; and support integrated enterprise alignment across Biomedical Research (BR), Development, Strategy & Growth (S&G), and the Commercial US and International units. About the Role Key Responsibilities: Brings external benchmarking, analysis and insights, and judgement to support the TA Strategy Head in developing a holistic Novartis TA strategy that achieves sustainable growth in short, mid and long-term. Brings both understanding of the pharmaceutical industry and the core Therapeutic Areas (TA) and Disease area of Oncology & Hematology to derive insightful and differentiating competitive advantages over our peers. Provides key commercial insights to the R&D project teams, particularly for early phase programs. To do this effectively, in-market experience in the US is critical. Analyses reports and publications to extract key messages, including building product forecasts. Supports development and delivery of TA-specific strategic external insights to support identification of growth opportunities, emerging competitive challenges and support creation of a third-party view around key strategic levers, and commissions targeted primary research. Essential Requirements: Bachelor's degree required. Advanced degree (PhD, MD or other advanced University degree) and / or equivalent experience in life science/healthcare; MBA or consulting or equivalent experience highly preferred. In-depth TA knowledge (or track record to acquire required TA expertise effectively and rapidly) in Oncology and Hematology. Highly agile having the capacity to support a number of strategic DAs within a TA and multiple programs internal and external Substantial experience evaluating new product opportunities (through M&A, BD&L and internal re-search programs). At least 5-7 years of Industry pharma and/or medical devices Experience in Research & Development and/or commercial functions with experience conducting, commissioning, analyzing primary research Experience of strategy development and asset shaping early in lifecycle (any functional perspective) Recent (post 2015) local US in-market experience; local US experience includes working within the US market with the local US customers, US health care systems / systems 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary #LI-hybrid Location: Basel, Switzerland Relocation Support: This role is based in Basel, Switzerland. Novartis is unable to offer relocation support: please only apply if accessible. This is one of two job postings a which may be based in either the United States (Cambridge) or Switzerland (Basel) Please ensure you apply for the position in the correct location and that it is is accessible for you Closing date for applications: 2 weeks from initial date of posting Are you excited by the challenge of finding what’s next in biomedical innovation? In this role you will help shape the future of Novartis’ pipeline by identifying, evaluating, and prioritising innovative external opportunities. This is a highly visible role where science, strategy, and partnership come together. In this hybrid role, you will gain breadth by supporting our engagement with venture capital partners and incubators across therapeutic areas, and depth by supporting coverage of one of our therapeutic area pillars. You will work at the forefront of therapeutic discovery and development, engaging with venture capital partners, biotech innovators, and internal experts to ensure Novartis continues to bring transformational medicines to patients worldwide. If you are curious, analytical, and motivated by impact, this is an opportunity to influence decisions that truly matter. About the Role Support search and evaluation initiatives aligned with Novartis strategy Help manage strategic relationships with venture capital firms and external innovation partners, analyze trends across therapeutic areas Identify, screen, and evaluate external programs and technologies across the development value chain, with an initial focus on neuromuscular disease Develop deep expertise in neuromuscular disease trends, science, and emerging technologies Drive proactive opportunity landscaping, catalyst mapping, and best practice sharing Partner closely with Research, Development, Commercial, and Strategy teams Prepare clear, compelling recommendations for senior governance and leadership forums Essential Requirements Advanced degree in life sciences, or a bachelor’s degree in life sciences with a Master of Business Administration Experience in business development, strategy, consulting, or pharmaceutical research and development Strong understanding of drug discovery, clinical development, and commercialisation processes Proven ability to work effectively in a global, matrixed environment Excellent analytical, communication, and stakeholder engagement skills Willingness to travel internationally 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 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Job ID REQ-10076037 May 08, 2026 Switzerland Summary The Biomedical Research (BR) division is the innovation engine of Novartis, focusing on novel approaches to generate therapeutic breakthroughs for patients. The Discovery Sciences department (DSc) at BR drives drug discovery projects and champions innovative novel drug modalities. The DNA-encoded chemical library (DEL) group in DSc Basel/Switzerland, is seeking a highly motivated, curious, and innovative Research Scientist who is eager to make an impact on drug discovery. Our mission is to accelerate the identification and optimization of novel low molecular weight (LMW) drugs, radioligand therapeutics (RLTs), siRNAs and other emerging therapeutic modalities with state-of-the-art technologies. Specifically, we apply and develop DEL technology to discover LMW and peptide binders to disease-relevant targets as a novel path to medicines. Our group is part of the larger Drug Discovery home in DSc, a highly collaborative group working at the interface of biology and chemistry to advance drug discovery. About the Role Position Location: onsite, Basel, CH #LI-onsite The DNA-encoded chemical library (DEL) group in DSc Basel/Switzerland, is seeking a highly motivated, curious, and innovative Research Scientist who is eager to make an impact on drug discovery. Our mission is to accelerate the identification and optimization of novel low molecular weight (LMW) drugs, radioligand therapeutics (RLTs), siRNAs and other emerging therapeutic modalities with state-of-the-art technologies. Specifically, we apply and develop DEL technology to discover LMW and peptide binders to disease-relevant targets as a novel path to medicines. Our group is part of the larger Drug Discovery home in DSc, a highly collaborative group working at the interface of biology and chemistry to advance drug discovery. Key Responsibilities: Conduct all experimental aspects related to DEL screening for early drug discovery projects, including the preparation of key reagents Execute DEL screening campaigns, interpret results, recognize when procedures are not working, and support troubleshooting Experimentally innovate and further develop existing DEL selection methods (e.g. towards emerging modalities) Analyze experimental data and communicate results at internal meetings Closely work within multidisciplinary, collaborative project teams and contribute to a constructive team environment Essential Requirements: MS equivalent (e.g., university degree, etc.) in scientific discipline such as biology, chemistry or pharmacology; or BS/apprenticeship (or equivalent) with appropriate and relevant experience in drug discovery Strong wet-lab experience in molecular biology, biochemistry and/or biophysics with a focus on manipulation and analysis of oligonucleotides and proteins Ability to adapt to scientific challenges and to generate innovative solutions Enthusiasm for exploring novel technologies and approaches to advance drug discovery Collaborative and self-motivated team player, with critical scientific and technical thinking Excellent interpersonal and organizational skills Good communication skills in oral and written English Desirable requirements: Interdisciplinary interest at the interface of chemistry, biology, and technology Practical and/or theoretical knowledge with encoded library screening: e.g. DEL, mRNA- or phage-display Experience with applying and developing computational tools for analyzing large data sets Experience in identifying and characterizing LMW and peptide ligands Programming experience in the areas of lab automation and NGS data analysis Familiarity with working in a highly productive and fast-paced environment *Please note that restrictions on flexible working may apply and will be discussed at interview stage if applicable 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 Benefits and Rewards: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Biomedical Research Business Unit Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Play Play 00:00 Play Seek 10 seconds backwards Seek 10 seconds forward 00:00 / 01:54 Mute Click to volume controlUse the arrows to control the volume Settings Turn on Picture in picture Show Full screen Research & Development Biomedical Research Switzerland Job ID REQ-10076037 Research Scientist, DNA-encoded chemical libraries (DEL) (80-100%*) Apply to Job (link is external)

Summary The Biomedical Research (BR) division is the innovation engine of Novartis, focusing on novel approaches to generate therapeutic breakthroughs for patients. The Discovery Sciences department (DSc) at BR drives drug discovery projects and champions innovative novel drug modalities. The DNA-encoded chemical library (DEL) group in DSc Basel/Switzerland, is seeking a highly motivated, curious, and innovative Research Scientist who is eager to make an impact on drug discovery. Our mission is to accelerate the identification and optimization of novel low molecular weight (LMW) drugs, radioligand therapeutics (RLTs), siRNAs and other emerging therapeutic modalities with state-of-the-art technologies. Specifically, we apply and develop DEL technology to discover LMW and peptide binders to disease-relevant targets as a novel path to medicines. Our group is part of the larger Drug Discovery home in DSc, a highly collaborative group working at the interface of biology and chemistry to advance drug discovery. About the Role Position Location: onsite, Basel, CH #LI-onsite The DNA-encoded chemical library (DEL) group in DSc Basel/Switzerland, is seeking a highly motivated, curious, and innovative Research Scientist who is eager to make an impact on drug discovery. Our mission is to accelerate the identification and optimization of novel low molecular weight (LMW) drugs, radioligand therapeutics (RLTs), siRNAs and other emerging therapeutic modalities with state-of-the-art technologies. Specifically, we apply and develop DEL technology to discover LMW and peptide binders to disease-relevant targets as a novel path to medicines. Our group is part of the larger Drug Discovery home in DSc, a highly collaborative group working at the interface of biology and chemistry to advance drug discovery. Key Responsibilities: Conduct all experimental aspects related to DEL screening for early drug discovery projects, including the preparation of key reagents Execute DEL screening campaigns, interpret results, recognize when procedures are not working, and support troubleshooting Experimentally innovate and further develop existing DEL selection methods (e.g. towards emerging modalities) Analyze experimental data and communicate results at internal meetings Closely work within multidisciplinary, collaborative project teams and contribute to a constructive team environment Essential Requirements: MS equivalent (e.g., university degree, etc.) in scientific discipline such as biology, chemistry or pharmacology; or BS/apprenticeship (or equivalent) with appropriate and relevant experience in drug discovery Strong wet-lab experience in molecular biology, biochemistry and/or biophysics with a focus on manipulation and analysis of oligonucleotides and proteins Ability to adapt to scientific challenges and to generate innovative solutions Enthusiasm for exploring novel technologies and approaches to advance drug discovery Collaborative and self-motivated team player, with critical scientific and technical thinking Excellent interpersonal and organizational skills Good communication skills in oral and written English Desirable requirements: Interdisciplinary interest at the interface of chemistry, biology, and technology Practical and/or theoretical knowledge with encoded library screening: e.g. DEL, mRNA- or phage-display Experience with applying and developing computational tools for analyzing large data sets Experience in identifying and characterizing LMW and peptide ligands Programming experience in the areas of lab automation and NGS data analysis Familiarity with working in a highly productive and fast-paced environment *Please note that restrictions on flexible working may apply and will be discussed at interview stage if applicable 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Location: Basel, Switzerland #onsite Role Purpose: As a Senior Expert Science & Technology in Downstream Process Development, you will play a key role in advancing model‑based development and decision making for biologics purification processes. You will develop, apply, and deploy mechanistic and hybrid models with a strong focus on chromatography, while also covering other downstream unit operations and their interconnection into integrated process flows. This role combines deep scientific expertise, hands‑on experimental work, and digital implementation. You will work closely with project teams, process development scientists, data scientists, and manufacturing stakeholders, and you will be an active member of a global modelling community shaping the future of downstream development at Novartis. About the Role In this role, you will: Develop and apply downstream process models for biologics, with a strong emphasis on chromatography (e.g. IEX, HIC, MMC, affinity) and their underlying physicochemical principles. Extend modelling approaches to other downstream unit operations (e.g. filtration, UF/DF, viral inactivation) and connect individual steps into integrated DSP models to support process understanding and optimization. Design, plan, and execute laboratory experiments to generate high‑quality data for model development, calibration, and validation, working hands‑on in the lab when required. Use modelling to support process design, scale‑up, troubleshooting, robustness studies, and decision making across early and late development. Implement and deploy models using Python, including development of user‑friendly tools or apps that enable broader adoption by project teams and stakeholders. Translate complex modelling results into clear, actionable insights for multidisciplinary audiences, including process scientists, project leaders, and management. Collaborate and communicate effectively with internal and external stakeholders, ensuring alignment between modelling activities, experimental work, and project objectives. Actively contribute to and help shape the global modelling community, sharing best practices, methodologies, and innovations across sites and functions. Contribute to scientific documentation, technical reports, and regulatory‑relevant deliverables as required. What you will bring Education & experience MSc, PhD, or equivalent experience in Biotechnology, Chemical Engineering, Biochemistry, or a related field. Several years of experience in biologics downstream process development, with demonstrated focus on process modelling. Strong, hands‑on expertise in chromatography, including mechanistic understanding of separation phenomena. Technical expertise Proven experience in downstream process modelling, ideally including chromatography modelling, parameter estimation, scale‑down/scale‑up concepts, and integration of multiple unit operations. Ability to design and run experiments to support model development and validation. Strong programming skills in Python, with experience in building reusable tools, workflows, or applications for broader user groups. Familiarity with data analysis, visualization, and model deployment concepts is a strong advantage. 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary #LI-Hybrid Internal job title: Director Location: Basel, Switzerland Translational Medicine Discovery & Profiling (TMDP) is a group of physicians and clinical researchers who drive innovative science from discovery to the patient through the selection, profiling, and early clinical development of medicines. Medical directors oversee phase 1 first-in-human (FiH) and phase 2 proof-of-concept (PoC) and dose range finding (DRF) studies in support for Phase 3 development. Medical directors in translational medicine are key and highly visible members of global cross-functional project teams that design and implement early research and discovery projects. Medical directors in translational medicine collaborate with colleagues in biology and chemistry to identify targets in diseases with significant unmet medical needs and provide input on likely clinical development pathways, design clinical development plans in collaboration with late phase development, draft clinical trial protocols and serve as medical leads for these trials. As a Medical Director in Translational Medicine Gastroenterology, you will report to the TM Head. About the Role Key Responsibilities: Lead global clinical trial teams through phase 1 and 2 development Draft the early clinical development plan Act as medical lead for early clinical studies Represent the team in relevant decision boards Serve a primary contact for internal and external key opinion leaders Oversee publication and internal/external presentation of clinical study results Work closely with biomarker experts in implementation Collaborate with research scientists to identify, develop and implement strategy for preclinical support of program related objectives Actively participate in Health Authority interactions Essential Requirements: Medical doctor with board certification in gastroenterology. Several years of clinical experience treating IBD (UC and CD) patients. Ability to learn fast and work independently Ability to lead multidisciplinary teams in a matrix organization. Excellent communication and presentation skills Desirable Requirements: Research experience (e.g., Ph.D.) is a plus but not a strict requirement Drug development experience as trial investigator or pharma experience are a plus but not strict requirements. Publications in the field of IBD are a plus but not a strict requirement 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary #Hybrid Location: Basel, Switzerland Relocation Support: This role is based in Basel Switzerland. Novartis is unable to offer relocation support: please only apply if accessible. At Novartis, we’re reimagining medicine—and how we protect the innovation behind it. We’re looking for an experienced Patent Litigation Paralegal to play a pivotal role in managing and modernising global patent litigation operations within a dynamic, high impact in house IP team. This is a hands on, senior paralegal role designed for someone who thrives in complex litigation environments, enjoys operational ownership, and wants to influence how litigation is run at scale. You will work closely with in house counsel, external law firms, and global stakeholders—bringing structure, foresight, and operational excellence to critical patent matters worldwide. You will act as the operational backbone of patent litigation matters, ensuring cases run smoothly, data is accurate and actionable, and stakeholders stay aligned. Beyond day to day case support, you’ll help drive smarter, more digital ways of working—using data, systems, and process improvements to enhance litigation quality and decision making. If you’re an experienced paralegal ready to step into a senior, high impact role—we’d love to hear from you. About the Role Independently support in‑house patent litigation counsel on enforcement and defence matters Serve as the operational lead for litigation cases: tracking milestones, maintaining documentation, and driving timely follow‑up on actions Coordinate seamlessly with external counsel, business partners, finance, and global IP stakeholders Maintain accurate, audit‑ready records to support strong reporting, forecasting, and governance Prepare clear meeting summaries, action logs, and status updates to keep matters moving forward Support litigation budget planning and forecasting, working closely with counsel and finance partners Lead and contribute to process improvements, workflows, and templates—including the practical use of digital tools and AI where appropriate Act as a central point of contact for information flow across regions, ensuring effective document and data management Essential Extensive experience as a Patent / IP Litigation Paralegal, either in‑house at a multinational company or within an IP litigation law firm Proven ability to manage complex litigation support work autonomously, with minimal supervision Strong organisational skills with the ability to prioritise across multiple matters and stakeholders Experience preparing schedules, trackers, and supporting documentation for attorney review Confidence communicating with internal business partners and external counsel across multiple countries High integrity, reliability, and a service‑oriented mindset Excellent written and spoken English Desirable Paralegal qualification, certification, or equivalent professional experience Exposure to litigation budgeting, forecasting, or analytics Interest in process improvement, digitalisation, and new ways of working Demonstrated leadership or mentoring capability within a paralegal function Commitment to Diversity & Inclusion: We are 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 any order to receive more detailed information about essential functions of a position, please send an e-mail to E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Job ID REQ-10077055 May 04, 2026 Switzerland Summary Novartis is a place where bright, curious minds combine to solve the world-s toughest healthcare challenges and reimagine medicine together. It-s an inspiring environment for aspiring talent. For those embarking on a career in innovative medicines or moving into the industry it-s an opportunity to gain early exposure, experience and insights that are hard to find anywhere else. Biomedical Research-s global Translational Medicine (TM) group builds on basic research advances to develop new therapies that address unmet medical need. We are the crucial bridge between drug discovery and clinical application. Through our work, we increase the speed, quality and productivity of drug discovery and development by Novartis and play a pivotal role in bringing innovative medicines to patients. Help us to unleash the power of translational safety science for drug discovery and development, bringing innovative medicines to patients, by building on research advances to develop new therapies, and bridging drug discovery and clinical application. The TM Academy is a cross-functional program within TM designed for career starters, career changers, and career relaunchers. If you are ready for two transformative years to gain hands-on experience in a diverse, multicultural, global and inclusive environment in early drug development and clinical trials, contributing to innovative programs and projects that help bring breakthrough treatments closer to patients worldwide, then this is the opportunity for you! About the Role This advert is exclusively f** or Preclinical Safety - Data Science within the TM Academy**. Other TM Academy roles are advertised separately under: REQ-10076855 -TM Academy Clinical Science & Innovation (CS&I) REQ-10077029 - TM Academy Pharmacokinetic Sciences (PKS) Modeling & Simulation REQ-10077246 - TM Academy Fellow in Biomarker Development REQ-10076845 - TM Academy Biomarker Development Laboratory Excellence and Operations (BMD LEO) Location: Basel, Switzerland Duration of program: 24 months Program start: 01 September 2026 Applications are open until 17-May-2026 included. By submitting your application, you confirm that you would be available to begin the program on 01-September, with final selection decisions expected to be communicated by end of June/early July. Please note that we can only accept applicants who are eligible to work in Switzerland. The TM Academy is designed for individuals with diverse backgrounds and experiences: - Career starters: recent university degree graduate within the past 2 years - Career changers: professionals with experience from a different field - Career relaunchers: professionals wanting to return to work after a career break JOB DESCRIPTION Your journey begins with a basecamp: 4-week immersive blended experience designed to introduce you to our organization, the drug development process, the various departments in Translational Medicine, the clinical trial process and the tools and technical platforms needed for your work. Throughout the program, fellows reunite for continuous learning focused on soft skills, cross-functional exposure, and thematic introduction series - broadening your perspective beyond your immediate team and function. As TM Academy fellow in PCS Data Science, you will have the opportunity to gain knowledge and contribute to one or more of our global inter-disciplinary teams including Translational Toxicology, Mechanistic & Predictive Safety, Pathology and Therapeutic Area Safety Assessment. Your contributions will support project teams throughout the Research & Development lifecycle spanning a diverse range of disease areas and therapeutic modalities. During the TM Academy you will- build a strong foundation in translational medicine with support from industry experts embark on a progressive, blended and flexible learning experience covering conceptual, theoretical and experiential techniques be part of a global network of supportive peers and mentors who will guide you to work and collaborate on meaningful projects that shape the future of medicine gain hands-on experience by contributing to and supporting a range of activities in translational safety assessments using computational approaches broaden your professional horizon by doing a deep dive in different areas aligned with your interests and based on open opportunities have the opportunity to teach back and mentor new fellows Role requirements Candidates should have: Demonstrated experience in working with large-scale biological datasets (e.g., genomics, transcriptomics, imaging, preclinical/clinical data) MSc or PhD or equivalent experience in quantitative field (computational sciences, physics, mathematics, economics, computational biology, machine learning, data science or related field) Strong programming skills in python/R, including agentic coding Strong grasp of statistics and machine learning Experience with reproducible data science tools and practices Fluency in business-level English; oral & written Good organizational, interpersonal, collaboration, and communication skills Ability to work in a team and independently, managing multiple priorities with support 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. 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: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Biomedical Research Business Unit Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Others Job Type Full time Employment Type Early Career (Fixed Term) Shift Work No Others Biomedical Research Switzerland Job ID REQ-10077055 Translational Medicine Academy fellow in Preclinical Safety - Data Science Apply to Job (link is external)

Summary Novartis is seeking passionate individuals to join our innovative team. You will work with cutting-edge technology, collaborate with experts, and drive excellence in patient safety. If you're eager to advance your career and be part of a forward-thinking company, we want you on our team! About the Role This is a director level role and can be based in Basel, Switzerland or London, UK (REQ-10077130 ) or Barcelona, Spain (REQ-10077131). Location: Basel, Switzerland Working pattern: Hybrid If you are interested in one of the other locations please apply on the REQ number for that location. Key Responsibilities: Safety Input and Team Participation: Provide expert safety input to the clinical development program for assigned projects/products and actively participate in the Global Program Team (GPT), Global Clinical Team (GCT), and Clinical Trial Team (CTT). Lead the Safety Management Team (SMT). Responsible for managing safety issues from the formation of the GPT through Life Cycle Management. Safety Strategy Preparation: Own the projects/products safety strategy and lead the production of medical safety deliverables. Core Global Labelling: Responsible for initial development and ongoing maintenance of safety information in Core Data Sheet, addressing safety issues in all project/product indications. Signal Detection and Safety Management: Oversee overall signal detection, monitoring, evaluation, interpretation, and appropriate management of safety information, based on data from all relevant sources. Regulatory and Professional Inquiries: Lead the preparation of the safety strategy for health authority responses and collaborate with other project team members. Respond to inquiries from regulatory authorities or healthcare professionals regarding safety issues. Departmental and Functional Goals: Contribute to and often lead the development of departmental and functional/business unit goals and objectives. Proactively engages in the development of competencies across the Medical Safety Function Role Requirements: Medical Degree or equivalent is preferred; PhD, PharmD or equivalent graduate level health care professional degree required 3 years clinical experience postdoctoral At least 5 years’ experience in drug development within a major pharmaceutical company, including: - A minimum of 2 years in a global role, and - At least 2 years’ experience in drug safety in an operational or medical capacity. Experience in clinical trial methodology, regulatory requirements, scientific methodology, statistics and writing of publications Expertise in preparing or contributing to preparation of clinical safety assessments and regulatory reports/submissions involving safety information Experience with (safety or others) issue management Experience in leading cross-functional, multicultural teams Languages : Fluent English (both spoken and written) is mandatory. Additional Desirable Skills: Additional languages are desirable Oncology experience would be an advantage Bring your global safety leadership to an organization where your expertise will directly influence patient safety, regulatory confidence, and successful drug development worldwide—apply now. 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Novartis is a place where bright, curious minds combine to solve the world’s toughest healthcare challenges and reimagine medicine together. It’s an inspiring environment for aspiring talent. For those embarking on a career in innovative medicines or moving into the industry it’s an opportunity to gain early exposure, experience and insights that are hard to find anywhere else. Biomedical Research’s global Translational Medicine (TM) group builds on basic research advances to develop new therapies that address unmet medical need. We are the crucial bridge between drug discovery and clinical application. Through our work, we increase the speed, quality and productivity of drug discovery and development by Novartis and play a pivotal role in bringing innovative medicines to patients. Biomarker solutions are critical in clinical development to: define the stage/subtype of the disease; predict the effect of medication; select a group of patients who would benefit most from a given therapy; and identify opportunities for development of companion diagnostics. Our scientists identify and use a wide range of biomarkers to investigate a disease, profile a compound’s mechanism of action, potency and likely side effects, select patients who may respond to therapy based on their genetic profile; and develop parallel/expanded indications for the compound. The TM Academy is a cross-functional program within TM designed for career starters, career changers, and career relaunchers. If you are ready for two transformative years to gain hands-on experience in a diverse, multicultural, global and inclusive environment in early drug development and clinical trials, contributing to innovative programs and projects that help bring breakthrough treatments closer to patients worldwide, then this is the opportunity for you! About the Role This advert is exclusively for Biomarker Development (BMD) Molecular, Cellular & Soluble Sciences (MCS) within the TM Academy . Other TM Academy roles are advertised separately under: REQ‑10076845 – TM Academy Biomarker Development Laboratory Excellence and Operations (BMD LEO) REQ-10076855 –TM Academy Clinical Science & Innovation (CS&I) REQ‑10077029 – TM Academy Pharmacokinetic Sciences (PKS) Modeling & Simulation REQ‑10077055 – TM Academy Preclinical Safety – Data Science Location : Basel, Switzerland Duration of program : 24 months Program start : 01-September- 2026 Applications are open until 17-May-2026 included. By submitting your application, you confirm that you would be available to begin the program on 01-September, with final selection decisions expected to be communicated by end of June/early July. Please note that we can only accept applicants who are eligible to work in Switzerland. JOB DESCRIPTION Your journey begins with a basecamp: 4-week immersive blended experience designed to introduce you to our organization, the drug development process, the various departments in Translational Medicine, the clinical trial process and the tools and technical platforms needed for your work. Throughout the program, fellows reunite for continuous learning focused on soft skills, cross-functional exposure, and thematic introduction series - broadening your perspective beyond your immediate team and function. As TM Academy fellow in BMD, you will receive training and mentorship, you will be empowered to do and learn and you will work in a diverse, multicultural, global and inclusive environment. Key learning areas include: Work as a tissue biomarker subject matter expert in clinical studies. Work with biomarker and pathologist experts to develop tissue biomarker plans and assays for implementation in clinical studies. Work with internal and external stakeholders to resolve issues related to tissue biomarker assessment in ongoing clinical trials. Learn and contribute to processes tailored to implement tissue biomarkers in clinical trials. Work and collaborate with PCS. Contribute to technology innovation for human tissue protein assessment. During the TM Academy you will… build a strong foundation in translational medicine with support from industry experts embark on a progressive, blended and flexible learning experience covering conceptual, theoretical and experiential techniques be part of a global network of supportive peers and mentors who will guide you to work and collaborate on meaningful projects that shape the future of medicine gain hands-on experience by contributing to and supporting: singleplex and multiplex tissue imaging while contributing to the establishment of critical in‑house capability in spatial data analysis within the BMD‑PCS Tissue Biomarker Laboratory. day‑to‑day implementation of singleplex and multiplex immunohistochemistry and immunofluorescence workflows , from histology/ tissue processing and staining through image acquisition, and will contribute to downstream data analysis and standardization efforts supporting innovative Translational Medicine programs. broaden your professional horizon by doing a deep dive in different areas aligned with your interests and based on open opportunities. have the opportunity to teach back and mentor new fellows Gain broad exposure to translational biomarker science , from experimental execution to data interpretation. Develop technical independence, scientific rigor, and cross‑functional collaboration skills in a real TM program setting. take laboratory‑based responsibilities (70-80% of time): Perform hands‑on singleplex and multiplex immunohistochemistry and immunofluorescence experiments on multiple platforms , including: Tissue preparation and handling Antibody panel application and staining workflows Instrument operation and run QC Support the establishment and optimization of internal laboratory workflows for tissue imaging within the BMD‑PCS lab environment. Work closely with pathologists and histology experts to ensure biological and technical data quality . Contribute to documentation and standardization of laboratory procedures to enable reproducibility and scalability. Contribute to data analysis (20-30% of time): Contribute to downstream image and spatial data analysis , including: Image quality control and preprocessing Cell segmentation and phenotypic annotation Basic spatial analysis and result visualization Translate laboratory outputs into clear, interpretable results for TM project teams. Role requirements Education • PhD in life sciences, biomedical sciences, bioengineering, pathology‑related disciplines , or a related field, completed or close to completion by start date. • Mandatory laboratory expertise: Demonstrated hands‑on laboratory experience with the following: - Single and multiplex immunohistochemistry - Single and multiplex in situ hybridization • Strong interest in experimental method development and laboratory innovation. Data & computational skills: • Mastery of image analysis is expected, using software such as Halo, Visiopharm, etc • Familiarity with image‑based or single‑cell data analysis is desired; deep expertise is not mandatory at entry. • Basic experience with Python and/or R for data exploration or analysis is an advantage. Mindset & working style: • Comfortable working at the bench on a daily basis • Curious, detail‑oriented, and motivated by emerging technologies • Collaborative and open to learning across laboratory, pathology, and data science interfaces 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary We offer two 6-month legal traineeship positions in Legal for Corporate Functions, one starting on January 1, 2027, and one starting on June 1, 2027! About the Role Are you interested in pursuing a career in law? We have the perfect opportunity for you! Our legal trainee position offers excellent hands-on, in-house legal experience within the dynamic and multinational environment of a leading pharmaceutical company. More than 70’000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world. We are seeking a motivated and diligent legal trainee who has the courage to navigate in unknown and ambiguous legal areas and has the curiosity to learn and being exposed to interesting and challenging new legal questions. If you're passionate about making a difference and keen to kickstart your career with our in-house team, this could be the ideal role for you. We offer two 6-month legal traineeship positions in Legal for Corporate Functions, one starting on January 1, 2027, and one starting on June 1, 2027. Your responsibilities include: • You'll be the backbone of our Legal team, offering essential advice in employment law (including questions related to Diversity, Equity & Inclusion), as well as litigation and investigation. You'll have the opportunity to tackle complex global and local issues, transforming challenges into solutions. • You'll get your hands on practical tasks, managing individual legal cases, but also major projects (e.g. related to reorganizations, divestments, implementation of new policies and processes, artificial intelligence, etc.), drafting and reviewing agreements, internal regulations, and templates. This is your chance to shift from theory to practical application, making an immediate impact. • Your role will involve in-depth legal research and the creation of legal memoranda, helping us to break down complex ideas into digestible insights. Here, your knowledge will fuel our mutual success. What you’ll bring to the role: • Swiss Bachelor of Law (BLaw) und Master of Law (MLaw); master degree needs to be completed before start date • Excellent proficiency in English and German, both in verbal and written communication • High motivation and ability to work independently on challenging tasks and projects • Prior legal internship and knowledge in employment law is a plus Are you ready to sharpen your skills and inspire change? If you're excited to contribute and learn, apply now, and submit a cover letter that includes your motivation for the position and your availability regarding the two traineeships (i.e. starting date January 1, 2027 or June 1, 2027). 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 E-Mail schreiben , 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Job ID REQ-10073942 Mar 19, 2026 Switzerland Summary We are seeking an enthusiastic and motivated PK Sciences project team representative to develop and implement translational or clinical pharmacology strategies to support the pursuit of transformative new medicines through late clinical development. Our unique organizational structure enables colleagues to work seamlessly in the translational and/or clinical space, offering opportunities for development and bench-to-bedside-to-bench translation. Experience in late discovery into clinical development is preferred. The scope of the role potentially includes small molecules, biologics/therapeutic proteins, antibody drug-conjugates, radioligand therapies and/or cell therapies across major therapeutic areas in Novartis, including oncology, immunology, cardiovascular renal metabolism, neuroscience, and global health. This position drives close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), and Operations through PK science sub-teams to achieve a holistic and integrative perspective of the ADME/clinical pharmacology properties of candidates and drugs. Collaborates effectively with broader, cross-disciplinary project teams to ensure PKS strategies are well integrated into project plans and scientific discussions. About the Role #LI_Hybrid Location: Basel, Switzerland Key responsibilities: - Represent the PK Sciences function in project teams, interactions with stakeholders within the organization and interactions with regulatory agencies, as appropriate - Proactively contributes to developing drug candidates across Research Development and Commercial continuum, providing expert pharmacokinetic / drug metabolism and clinical pharmacology input - Work with teams to elucidate the understanding of PK/PD relationships and develop dosing strategies and predictions - Develop and execute clinical pharmacology strategies, including input into nonclinical and clinical study design, and analyzing PK and PK/PD data, to support compound development from discovery through late development - Provide PK, dosage, and PK/PD components of study protocols, reports, project summaries and development plans, and author pharmacokinetic/clinical pharmacology/biopharmaceutics sections of IND/IMPDs and NDA/BLAs as well as prepare appropriate responses to Health Authority questions - Drive close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), through PK science sub-teams. - Works in close collaboration with clinicians and clinical development colleagues to integrate PKS insights into study design, data interpretation, and project decision-making - Use of Artificial intelligence (AI) / Machine Learning (ML) approaches to enable model guided molecular design, preclinical and clinical data automation, authoring regulatory documents, and the use of predictive models This role reports to Therapeutic Area group in PK Sciences within Translational Medicine (TM) in Biomedical Research. PKS is a global organization situated within Translational Medicine (TM), the clinical research arm of Biomedical Research within Novartis. PK Sciences plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, bridging drug discovery and clinical application. PK Science is an enterprise-wide organization, working across both Biomedical Research and the Development organizations to advance the scientific knowledge of pharmacokinetics, metabolism and clinical pharmacology. Essential requirements: - Ph.D. / Pharm.D. with relevant experience in clinical pharmacology, drug metabolism and pharmacokinetics or a related background. - A minimum of 0-2 years of experience in drug discovery and/or development in a relevant environment (academia, CRO, biotech or Pharma). 2+ years of experience preferably in a lead role overseeing ADME/DMPK project strategy, either in discovery or clinical development to be considered for Principal Scientist II - Extensive and in-depth knowledge of pharmacokinetics including, drug metabolism and PK/PD evaluation, experience in working in project teams (preferably global) as well as sound awareness of recent developments in drug development and regulatory sciences. - Exposure to working in a cross-functional, matrixed, project-team environment. - Strong oral and written communication skills. Desirable Requirements: - Hands-on project experience with Artificial intelligence (AI) / Machine Learning (ML) approaches is a plus Leadership / Novartis Behaviors in Action - Delivers results through disciplined execution, continuous improvement, and a strong focus on value and outcomes. - Demonstrates an enterprise mindset and strong ownership by prioritizing resources and decisions for maximum Novartis and patient impact. - Role models Novartis leadership behaviors through visible actions, continuous self reflection, and openness to feedback - Builds trust through transparent communication, clear accountability, and consistent delivery against commitments. AI fluency: - Brings strong AI and digital fluency, using enterprise tools to enhance insight generation, decision making, and team productivity. **This is a dual level posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered. 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: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Biomedical Research Business Unit Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Play Play 00:00 Play Seek 10 seconds backwards Seek 10 seconds forward 00:00 / 01:54 Mute Click to volume controlUse the arrows to control the volume Settings Turn on Picture in picture Show Full screen Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Research & Development Biomedical Research Switzerland Job ID REQ-10073942 Principal Scientist I or II**, PK Sciences Therapeutic Areas Apply to Job (link is external)

Job ID REQ-10073941 Mar 19, 2026 Switzerland Summary We are seeking an enthusiastic and motivated PK Sciences project team representative to develop and implement translational or clinical pharmacology strategies to support the pursuit of transformative new medicines through late clinical development. Our unique organizational structure enables colleagues to work seamlessly in the translational and/or clinical space, offering opportunities for development and bench-to-bedside-to-bench translation. Experience in late discovery and/or clinical area is preferred. The scope of the role potentially includes small molecules, biologics/therapeutic proteins, antibody drug-conjugates, radioligand therapies and/or cell therapies across major therapeutic areas in Novartis, including oncology, immunology, cardiovascular renal metabolism, neuroscience, and global health. This position drives close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), and Operations through PK science sub-teams to achieve a holistic and integrative perspective of the ADME/clinical pharmacology properties of candidates and drugs About the Role #LI_Hybrid Location: Basel, Switzerland Key Responsibilities: - Independently represent the PK Sciences function in cross-functional project teams, interactions with stakeholders within the organization and interactions with regulatory agencies, as appropriate - Lead a PK Science Subteam with interdisciplinary representation of the major functions from within PK Science and beyond - Ensures implementation of project strategies and monitors timelines, objectives, and budgets for assigned projects - Present projects at various institutional review and approval boards - Proactively contributes to developing drug candidates across Research Development and Commercial continuum, providing expert pharmacokinetic / drug metabolism and clinical pharmacology input - Develop and execute clinical pharmacology strategies, including input into nonclinical and clinical study design, and analyzing PK and PK/PD data, to support compound development from discovery through late development - Provide PK, dosage, PK/PD and M&S component of study protocols, reports, project summaries and development plans, and author pharmacokinetic/clinical pharmacology/biopharmaceutics sections/radiation dosimetry of IND/IMPDs and NDA/BLAs as well as prepare appropriate responses to global Health Authority questions - Use of Artificial intelligence (AI) / Machine Learning (ML) approaches to enable model guided molecular design, preclinical and clinical data automation, authoring regulatory documents, and the use of predictive models - Is a mentor to or manages junior associates in the organization This role reports to Therapeutic Area Head in PK Sciences within Translational Medicine (TM) in Biomedical Research. PKS is a global organization situated within Translational Medicine (TM), the clinical research arm of Biomedical Research within Novartis. PK Sciences plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, bridging drug discovery and clinical application. PK Science is an enterprise-wide organization, working across both Biomedical Research and the Development organizations to advance the scientific knowledge of pharmacokinetics, metabolism and clinical pharmacology. Essential Requirements: - Ph.D. / Pharm.D. with relevant experience - Preferred candidates will have a minimum of 5+ yrs at the Senior Principal Scientist Level and 8+ years at the Associate Director level) in clinical pharmacology, drug metabolism and pharmacokinetics or a related background in an industry setting. - Extensive and in-depth knowledge of pharmacokinetics including, drug metabolism and PK/PD evaluation, experience in working in project teams (preferably global) as well as sound awareness of recent developments in drug development and regulatory sciences. - Demonstrated success in working in a cross-functional, matrixed, project-team environment. - An influential Team player and talented negotiator with strong oral and written communication skills. - Proven record of mentorship and/or people management Desirable Requirements: - Hands-on project experience with Artificial intelligence (AI) / Machine Learning (ML) approaches is a plus Leadership / Novartis Behaviors in Action - Delivers results through disciplined execution, continuous improvement, and a strong focus on value and outcomes. - Demonstrates an enterprise mindset and strong ownership by prioritizing resources and decisions for maximum Novartis and patient impact. - Role models Novartis leadership behaviors through visible actions, continuous self reflection, and openness to feedback - Builds trust through transparent communication, clear accountability, and consistent delivery against commitments. - Empowers others to innovate and improve while maintaining high scientific, ethical, and operational standards. AI fluency: - Brings strong AI and digital fluency, using enterprise tools to enhance insight generation, decision making, and team productivity. - Accountable for the ethical, transparent, and compliant use of AI in line with Novartis AI governance and data protection standards. External eminence: - Acts as an external thought leader, advancing Novartis- reputation in translational science and innovation. Operational excellence: - Drives operational excellence through disciplined execution, continuous improvement, and effective use of resources to maximize PKS and enterprise value. - Acts as a responsible steward of people, data, and digital capabilities, leveraging AI and automation to improve efficiency, quality, and decision speed. *This is a dual level posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered. 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: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Biomedical Research Business Unit Research Location Switzerland Site Basel (City) Company / Legal Entity C028 (FCRS = CH028) Novartis Pharma AG Functional Area Research & Development Job Type Full time Employment Type Regular Shift Work No Play Play 00:00 Play Seek 10 seconds backwards Seek 10 seconds forward 00:00 / 01:54 Mute Click to volume controlUse the arrows to control the volume Settings Turn on Picture in picture Show Full screen Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve. Research & Development Biomedical Research Switzerland Job ID REQ-10073941 Senior Principal Scientist/Associate Director* PK Sciences Apply to Job (link is external)

Summary #LI-Hybrid Location: Basel, Switzerland The Executive Director Pricing & Contracting (EDPC) will work on CRM portfolio and is a partner/subject matter expert who is a reliable and visible contact point for priority countries. The EDPC is expected to drive strategic initiatives which position International Pricing as a key collaborator through partnership with relevant functions (TA, S&G, Access, HEOR, Policy, Finance, etc.). The EDPC will act as an advisor to other functions and senior management teams on specific pricing-related topics. Lead a team of pricing & contracting professionals, act as a role model by further strengthening the organizational culture, and by mentoring other talent within and outside of pricing. The EDPC will drive development of launch and in-market pricing strategies and contracting solutions for selected brands that enable access for our products in partnership with the TA teams, other partner functions and regions/key countries. The position is reporting to the Head of Pricing. About the Role Key Responsibilities: Leads a Pricing & Contracting team with a disruptive mindset to tackle competitive environments and develop innovative pricing strategies and tactics to support regions/countries in delivering expected results. Provides effective and inspiring team leadership, actively works on career development, and focuses on retaining and attracting top talent Work effectively across functions and geographies with a focus on customer needs to achieve goals and ensure key stakeholder alignment. A thought partner/subject matter expert who is a reliable and visible contact point for priority countries to provide active, effective key country-level support. Interact regularly with priority countries. Facilitate operational pricing scenario analysis on local price and innovative contract proposals for consultation and decision-making. Share overall pricing approach and strategies, as necessary, with the US organization. Educate senior leadership on the pricing and reimbursement landscape developments of priority countries as appropriate. In partnership with Policy and Healthcare Systems leads, identify pricing policy barriers/opportunities and develop strategic and operational plans to address the pricing components of key policy issues (e.g., global price transparency, EU co-operation initiatives). Provide/withhold endorsement of price proposals consistent with international governance at launch and any list & net price changes post-launch for assigned countries. Monitor local pricing implementation. Oversee vendor/consulting/internal projects aimed at answering strategic pricing and business questions. Executive Director Pricing & Contracting will partner with the TAs, HEOR, Access, Finance and other teams to: Develop, review, and execute pricing and innovative contracting strategies for key compounds/indications within assigned areas. Responsible for ensuring alignment with program and brand strategies to optimize brand value and market access. Collaborate on pricing research with other international functions, key countries/regions (as needed). Identify competitive trends, synthesize competitor price information (including biosimilars and generics), and trigger actions as required. Design and oversee international launch sequence optimization for assigned assets/indications. Coordinate with key countries and regions and other international functions to ensure pricing and access are optimized as impact is felt globally across markets. Develop and co-create models to optimize pricing and access and recommend adaptations where appropriate. Coordinates, as needed, input into the price assessment of early-stage products and due diligence projects to validate price, dosing, endpoint, and comparator selection from a price implementation and realization point of view. Essential Requirements: At least 7 years of relevant senior level experience at pharmaceutical companies, HTA or health care consultancy companies; pricing, access and commercial experience across multiple brands and multiple therapeutic areas. Excellent analytical skills and ability to extract and quickly process key information, summarize key needs, and provide targeted and appropriate insights and recommendations. Previous team management experience. Strategic thinker with strong business and finance acumen. Recent experience in above country (regional or global) role preferred. Experience or strong exposure to some of our priority markets (US, EU5, China, Japan) and preferably also to emerging key markets in LaCan and APMA. Track record of successfully working across functions (especially TAs, S&G, V&A, Finance). Experience in preparation and negotiating reimbursement and HTA submissions with payers in major markets. Desirable Requirements: 10+ years of relevant senior level experience Advanced degree (e.g. PhD, Masters) in Math, Economics, Business Administration, Finance, Marketing, Health Policy, Health Economics, or related fields. Accessibility statement for Switzerland Yes/No, If Yes: Yes Switzerland 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 E-Mail schreiben and let us know the nature of your request and your contact information. Please include the job requisition number in your message. Benefits: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: Novartis Life Handbook Commitment to Diversity & Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve. 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary At Translational Medicine (TM), we are committed to bringing breakthrough medicines to patients and bridging the gap between research and clinical application. TM plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, and bridging drug discovery and clinical application. At TM, our work directly impacts patients worldwide. During this intense 2-year program, you will receive training and mentorship, with the empowerment to learn and work in a diverse, multicultural, global and inclusive environment where innovation and revolution in medicine become a reality. If you are ready for a transformative experience and want to make a real impact on the lives of millions, then this is the opportunity for you! About the Role This advert is exclusively for Pharmacokinetics Sciences Modeling & Simulaton within the TM Academy . Other TM Academy roles are advertised separately under: REQ-10076855 –TM Academy Clinical Science & Innovation (CS&I) REQ‑10077055 – TM Academy Preclinical Safety – Data Science REQ‑10077246 – TM Academy Fellow in Biomarker Development REQ‑10076845 – TM Academy Biomarker Development Laboratory Excellence and Operations (BMD LEO) Location: Basel, Switzerland Duration of program: 24 months Program start: 01 September 2026 Applications are open until May 17 2026 included. By submitting your application, you confirm that you would be available to begin the program on 01-September, with final selection decisions expected to be communicated by end of June. Please note that we can only accept applicants who are eligible to work in Switzerland. TM Academy is designed for individuals with diverse backgrounds and experiences: Career starters: recent university degree graduate within the past 2 years Career changers: professionals with experience from a different field Career relaunches: professionals wanting to return to work after a career break JOB DESCRIPTION Your journey begins with a basecamp: 4-week immersive blended experience designed to introduce you to our organization, the drug development process, the various departments in Translational Medicine, the clinical trial process and the tools and technical platforms needed for your work. Throughout the program, fellows reunite for continuous learning focused on soft skills, cross-functional exposure, and thematic introduction series - broadening your perspective beyond your immediate team and function. As a TM Academy fellow in PKS Modeling & Simulation , you will apply your quantitative modeling expertise to advancing translational immunology. In this position, you will join our translational modeling & simulation team to develop a mechanistic, quantitative framework for B cell driven indications. With state-of-the-art mechanistic modeling, including physiologically-based pharmacokinetic (PBPK) and quantitative systems pharmacology (QSP) methods, you will help generate actionable insights for immune reset diseases, inform dose/schedule optimization, and translation from preclinical systems to patients. During the TM Academy you will Develop and implement a physiology-based PK/PD modeling framework that links drug exposure and target engagement to B-cell and plasma cell differentiation, trafficking, and turnover kinetics across blood, lymphoid tissues, and disease-relevant tissues Integrate translational evidence from in vitro / in vivo /early clinical data to estimate parameters and quantify uncertainty, and to connect tissue depletion depth/duration/recovery kinetics to immune-reset biomarkers to enable decision making across B-cell depleting modalities Communicate results in cross-functional settings through presentations, reports, and manuscripts; partner closely with immunology, translational, and modeling stakeholders Own an end-to-end, production-ready modeling platform and expand expertise at the interface of quantitative pharmacology and immunology, with opportunities for strong internal and external visibility Experience the impact of translational modeling for drug development in an industrial setting by inform dose and schedule optimization across a large portfolio of B-cell depleting therapies and indications Role requirements Candidates should have: PhD in quantitative pharmacology/pharmacometrics, bioengineering, systems biology, applied mathematics, biostatistics, computational biology, or a related discipline Hands‑on experience in building and evaluating mechanistic models (e.g., ODE/PDE, compartmental, systems pharmacology, PK/PD) Programming proficiency in at least one scientific language (e.g., Python, R, MATLAB SimBiology); ability to write reproducible, modular, well‑documented code Experience working with biological datasets (preclinical and/or clinical) including data cleaning, visualization, model fitting, and interpretation Strong communication and collaboration skills; ability to translate complex quantitative findings into clear biological and project implications These additional skills would be a plus: Background in immunology, particularly B‑cell biology, lymphoid tissue organization, or immune cell trafficking Experience modeling biologics and/or cell therapies, including target engagement and cell‑killing dynamics Familiarity with physiology‑based or multi‑compartment modeling of immune-cell dynamics in cell-based and T‑cell–redirecting therapies (CAR‑T cell therapy / T-cell engaging antibodies) Familiarity with PBPK concepts and software (e.g., mrgsolve, nlmixr2, NONMEM, Monolix, SimBiology, Stan, or comparable platforms) Coding portfolio related to mechanistic modelling or systems biology 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 E-Mail schreiben , 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Novartis is a place where bright, curious minds combine to solve the world’s toughest healthcare challenges and reimagine medicine together. It’s an inspiring environment for aspiring talent. For those embarking on a career in innovative medicines or moving into the industry it’s an opportunity to gain early exposure, experience and insights that are hard to find anywhere else. Biomedical Research’s global Translational Medicine (TM) group builds on basic research advances to develop new therapies that address unmet medical need. We are the crucial bridge between drug discovery and clinical application. Through our work, we increase the speed, quality and productivity of drug discovery and development by Novartis and play a pivotal role in bringing innovative medicines to patients. Biomarker solutions are critical in clinical development to: define the stage/subtype of the disease; predict the effect of medication; select a group of patients who would benefit most from a given therapy; and identify opportunities for development of companion diagnostics. Our scientists identify and use a wide range of biomarkers to investigate a disease, profile a compound’s mechanism of action, potency and likely side effects, select patients who may respond to therapy based on their genetic profile; and develop parallel/expanded indications for the compound. The TM Academy is a cross-functional program within TM designed for career starters, career changers, and career relaunchers. If you are ready for two transformative years to gain hands-on experience in a diverse, multicultural, global and inclusive environment in early drug development and clinical trials, contributing to innovative programs and projects that help bring breakthrough treatments closer to patients worldwide, then this is the opportunity for you! About the Role This advert is exclusively f or Biomarker Development Laboratory Excellence and Operations (BMD LEO) within the TM Academy . Other TM Academy roles are advertised separately under: REQ‑10077246 – TM Academy Fellow in Biomarker Development REQ-10076855 –TM Academy Clinical Science & Innovation (CS&I) REQ‑10077029 – TM Academy Pharmacokinetic Sciences (PKS) Modeling & Simulation REQ‑10077055 – TM Academy Preclinical Safety – Data Science Location: Basel, Switzerland Duration of program: 24 months Program start: 01 September 2026 Applications are open until 17-May-2026 included. By submitting your application, you confirm that you would be available to begin the program on 01-September, with final selection decisions expected to be communicated by end of June/early July. Please note that we can only accept applicants who are eligible to work in Switzerland. The TM Academy is designed for individuals with diverse backgrounds and experiences: Career starters: recent university degree graduate within the past 2 years Career changers: professionals with experience from a different field Career relaunchers: professionals wanting to return to work after a career break JOB DESCRIPTION Your journey begins with a basecamp: 4-week immersive blended experience designed to introduce you to our organization, the drug development process, the various departments in Translational Medicine, the clinical trial process and the tools and technical platforms needed for your work. Throughout the program, fellows reunite for continuous learning focused on soft skills, cross-functional exposure, and thematic introduction series - broadening your perspective beyond your immediate team and function. As TM Academy fellow in BMD LEO, you will receive training and mentorship, you will be empowered to do and learn and you will work in a diverse, multicultural, global and inclusive environment. Key learning areas include: Represent BMD on clinical trial teams; work with biomarker experts and clinical trial leaders to develop biomarker plans for implementation in clinical studies. Gain familiarity with innovative biomarker technologies used in clinical research. Develop relevant study documentation, including clinical protocol biomarker sections, lab manuals, informed consent forms and biomarker study budgets. Work with internal and external stakeholders to resolve issues related to biomarker samples in ongoing clinical trials. Acquire knowledge of potential ethical issues related to biomarker sample collection and analysis, and devise solutions that satisfy both ethical concerns and study objectives. Learning to perform logistical and operational activities for innovative biomarkers, coordinating with clinical sites, managing and tracking material supply and sample at sites, central lab, and external service providers. Monitor and provide oversight of biomarkers and laboratory assays (e.g. flow cytometry, Immunoassays) at external partners (CRO). Lead and contribute to process improvement projects, technology evaluation operational innovation and initiatives across BR sites During the TM Academy you will… build a strong foundation in translational medicine with support from industry experts embark on a progressive, blended and flexible learning experience covering conceptual, theoretical and experiential techniques be part of a global network of supportive peers and mentors who will guide you to work and collaborate on meaningful projects that shape the future of medicine gain hands-on experience by contributing to and supporting a biomarker plan execution in clinical studies broaden your professional horizon by doing a deep dive in different areas aligned with your interests and based on open opportunities have the opportunity to teach back and mentor new fellows ​ Role requirements Demonstrated interest in biomarker development and clinical research University degree (BA; BSc, MA, MSc, PharmD or PhD) or relevant professional experience Fluency in business-level English; oral & written Good organizational, interpersonal, collaboration, and communication skills Ability to work in a team and independently, managing multiple priorities with support Candidates should have: Good Office IT skills 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Novartis is a place where bright, curious minds combine to solve the world’s toughest healthcare challenges and reimagine medicine together. It’s an inspiring environment for aspiring talent. For those embarking on a career in innovative medicines or moving into the industry it’s an opportunity to gain early exposure, experience and insights that are hard to find anywhere else. Biomedical Research’s global Translational Medicine (TM) group builds on basic research advances to develop new therapies that address unmet medical need. We are the crucial bridge between drug discovery and clinical application. Through our work, we increase the speed, quality and productivity of drug discovery and development by Novartis and play a pivotal role in bringing innovative medicines to patients. Clinical Sciences & Innovation (CS&I) plans, designs and manages the clinical TM portfolio and partners with Global Clinical Operations to execute the TM clinical portfolio worldwide. Our associates strive to support a smooth transition from discovery research to clinical practice – driven by a strong focus on clinical & data sciences, clinical innovation, patient centricity and strategic planning. The TM Academy is a cross-functional program within TM designed for career starters, career changers, and career relaunchers. If you are ready for two transformative years to gain hands-on experience in a diverse, multicultural, global and inclusive environment in early drug development and clinical trials, contributing to innovative programs and projects that help bring breakthrough treatments closer to patients worldwide, then this is the opportunity for you! About the Role This advert is exclusively for Clinical Sciences & Innovation (CS&I) within the TM Academy . Other TM Academy roles are advertised separately under: REQ‑10077029 – TM Academy Pharmacokinetic Sciences (PKS) Modeling & Simulation REQ‑10077055 – TM Academy Preclinical Safety – Data Science REQ‑10077246 – TM Academy Fellow in Biomarker Development REQ‑10076845 – TM Academy Biomarker Development Laboratory Excellence and Operations (BMD LEO) Location : Basel, Switzerland Duration of program : 24 months Program start : 01-September- 2026 Applications are open until 17-May-2026 included. By submitting your application, you confirm that you would be available to begin the program on 01-September, with final selection decisions expected to be communicated by end of June/early July. Please note that we can only accept applicants who are eligible to work in Switzerland. The TM Academy is designed for individuals with diverse backgrounds and experiences: • Career starters: recent university degree graduate within the past 2 years • Career changers: professionals with experience from a different field • Career relaunchers: professionals wanting to return to work after a career break Your journey begins with a basecamp: 4-week immersive blended experience designed to introduce you to our organization, the drug development process, the various departments in Translational Medicine, the clinical trial process and the tools and technical platforms needed for your work. Throughout the program, fellows reunite for continuous learning focused on soft skills, cross-functional exposure, and thematic introduction series - broadening your perspective beyond your immediate team and function. As a TM Academy fellow in CS&I, you will have the opportunity to gain knowledge and contribute to the operational and logistical aspects of early phase clinical trials in TM across different therapeutic areas. In parallel to your Academy learning, your focus will be to provide support to the various CS&I groups and the clinical teams throughout the trial lifecycle – from set-up, through maintenance, and reporting. During the TM Academy you will… build a strong foundation in translational medicine with support from industry experts embark on a progressive, blended and flexible learning experience covering conceptual, theoretical and experiential techniques be part of a global network of supportive peers and mentors who will guide you to work and collaborate on meaningful projects that shape the future of medicine gain hands-on experience by contributing to and supporting a range of clinical trial operations activities such as: play a key role in shaping the quality of clinical, regulatory, and trial documents by ensuring that they are complete, accurate, consistent, and ready for submission support creating and refining important clinical documents - working closely with experienced colleagues who will guide you as you grow bring energy to team communications by crafting trial newsletters and helping organize engaging investigator and study‑related meetings learn the ins and outs of clinical trial documentation by supporting the setup and oversight of the Trial Master File facilitate communication and collaboration across global teams, investigator sites, and vendors by helping gather information and keeping activities moving smoothly build hands‑on experience with key clinical trial systems (CTMS, risk/issue tracking, site‑engagement tools), ensuring data is accurate and up to date support day‑to‑day trial operations - coordinating meetings, tracking materials, and keeping signatures and documentation flowing broaden your professional horizon by doing a deep-dive within one of the CS&I groups aligned with your interests and based on open opportunities, such as e.g. trial management, feasibility, study budget, data visualizations, clinical pharmacology, clinical innovation have the opportunity to teach back and help welcome new fellows by contributing to their onboarding and sharing what you’ve learned along the way Role requirements Candidates should have: Demonstrated interest in clinical research and drug development and curious to engage in a scientific environment focused on clinical trial operations enablement, documentation, and cross-functional coordination University degree (BA; BSc, MA, MSc, PharmD or PhD) or relevant professional experience Fluency in business-level English; oral & written Good organizational, interpersonal, collaboration, and communication skills ability to work in a team and independently, managing multiple priorities with support Good Office IT skills 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Novartis is a place where bright, curious minds combine to solve the world’s toughest healthcare challenges and reimagine medicine together. It’s an inspiring environment for aspiring talent. For those embarking on a career in innovative medicines or moving into the industry it’s an opportunity to gain early exposure, experience and insights that are hard to find anywhere else. Biomedical Research’s global Translational Medicine (TM) group builds on basic research advances to develop new therapies that address unmet medical need. We are the crucial bridge between drug discovery and clinical application. Through our work, we increase the speed, quality and productivity of drug discovery and development by Novartis and play a pivotal role in bringing innovative medicines to patients. Help us to unleash the power of translational safety science for drug discovery and development, bringing innovative medicines to patients, by building on research advances to develop new therapies, and bridging drug discovery and clinical application. The TM Academy is a cross-functional program within TM designed for career starters, career changers, and career relaunchers. If you are ready for two transformative years to gain hands-on experience in a diverse, multicultural, global and inclusive environment in early drug development and clinical trials, contributing to innovative programs and projects that help bring breakthrough treatments closer to patients worldwide, then this is the opportunity for you! About the Role This advert is exclusively f or Preclinical Safety – Data Science within the TM Academy . Other TM Academy roles are advertised separately under: REQ-10076855 –TM Academy Clinical Science & Innovation (CS&I) REQ‑10077029 – TM Academy Pharmacokinetic Sciences (PKS) Modeling & Simulation REQ‑10077246 – TM Academy Fellow in Biomarker Development REQ‑10076845 – TM Academy Biomarker Development Laboratory Excellence and Operations (BMD LEO) Location: Basel, Switzerland Duration of program: 24 months Program start: 01 September 2026 Applications are open until 17-May-2026 included. By submitting your application, you confirm that you would be available to begin the program on 01-September, with final selection decisions expected to be communicated by end of June/early July. Please note that we can only accept applicants who are eligible to work in Switzerland. The TM Academy is designed for individuals with diverse backgrounds and experiences: • Career starters: recent university degree graduate within the past 2 years • Career changers: professionals with experience from a different field • Career relaunchers: professionals wanting to return to work after a career break JOB DESCRIPTION Your journey begins with a basecamp: 4-week immersive blended experience designed to introduce you to our organization, the drug development process, the various departments in Translational Medicine, the clinical trial process and the tools and technical platforms needed for your work. Throughout the program, fellows reunite for continuous learning focused on soft skills, cross-functional exposure, and thematic introduction series - broadening your perspective beyond your immediate team and function. As TM Academy fellow in PCS Data Science, you will have the opportunity to gain knowledge and contribute to one or more of our global inter-disciplinary teams including Translational Toxicology, Mechanistic & Predictive Safety, Pathology and Therapeutic Area Safety Assessment. Your contributions will support project teams throughout the Research & Development lifecycle spanning a diverse range of disease areas and therapeutic modalities. During the TM Academy you will… build a strong foundation in translational medicine with support from industry experts embark on a progressive, blended and flexible learning experience covering conceptual, theoretical and experiential techniques be part of a global network of supportive peers and mentors who will guide you to work and collaborate on meaningful projects that shape the future of medicine gain hands-on experience by contributing to and supporting a range of activities in translational safety assessments using computational approaches broaden your professional horizon by doing a deep dive in different areas aligned with your interests and based on open opportunities have the opportunity to teach back and mentor new fellows Role requirements Candidates should have: Demonstrated experience in working with large-scale biological datasets (e.g., genomics, transcriptomics, imaging, preclinical/clinical data) MSc or PhD or equivalent experience in quantitative field (computational sciences, physics, mathematics, economics, computational biology, machine learning, data science or related field) Strong programming skills in python/R, including agentic coding Strong grasp of statistics and machine learning Experience with reproducible data science tools and practices Fluency in business-level English; oral & written Good organizational, interpersonal, collaboration, and communication skills Ability to work in a team and independently, managing multiple priorities with support 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Provide overall leadership, management, and strategic planning for the management of third-party service providers for the delivery of facility services at Campus Basel incl. Rotkreuz and Geneva. Fully support facility services within both direct contract and integrated facility management (IFM) models. Responsibilities include facility management of the overall buildings, grounds, cleaning, food services, infrastructure and site maintenance operations. Develop strategic relationships with third-party service providers and Novartis business stakeholders. Recognized as competent in evolving facilities management and strategic planning to build and sustain competitive advantage. Facilitate and participate in the development of change management approaches required to implement them. Ensure close coordination with, and actively participate in, REFS initiatives to maximize enterprise-wide opportunities Location: Basel, Switzerland #LI-Hybrid About the Role Key Responsibilities: Lead the region FM Team and govern third party service providers providing facility services to make sure that they adhere to baseline budgets, work to develop new scope of work, and maintain site operations 24/7 as necessary Conceptualize, develop, and implement innovative short- and long-term business strategies to improve quality, productivity, customer service levels and cost efficiency. Ensure the facility services meet end user requirements stakeholder customer satisfaction. Alignment with the Novartis Design & Construction Management (DCM) team on CODB plans prior to the DCM team executing the project plans. Partner with Novartis Procurement, e.g. to participate in the request for proposal process when evaluating new suppliers. Partner with HSE and QA teams for safety and compliance management to ensure proper compliance via third party service provider and all contracted vendors. Ensure effective third-party contract management and governance incl. service provider ratings for monthly/quarterly financial and operational performance indicators. Provide oversight and take corrective action quickly and decisively as required Demonstrate company values on a consistent basis. Drive culture within organization that retains and develops talent to create a pipeline for organizational growth, as well as one which values diversity and embraces inclusive behaviors. Essential Requirements: 5+ years of experience in a facility management/ maintenance environment Strong financial competency with budgeting, capital planning and maintenance Extensive pharmaceutical facility operation experience Strong knowledge of facility/ building/ utility operations and services, and the ability to understand corporate perspective, strategic and financial incl. regulatory knowledge as related to pharmaceutical industry Strong stakeholder management and influencing without formal authority skills Ability to manage ambiguity and complexity in evolving environments Strong communication skills in English/German, both written and verbal 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary We are seeking an enthusiastic and motivated PK Sciences project team representative to develop and implement translational or clinical pharmacology strategies to support the pursuit of transformative new medicines through late clinical development. Our unique organizational structure enables colleagues to work seamlessly in the translational and/or clinical space, offering opportunities for development and bench-to-bedside-to-bench translation. Experience in late discovery into clinical development is preferred. The scope of the role potentially includes small molecules, biologics/therapeutic proteins, antibody drug-conjugates, radioligand therapies and/or cell therapies across major therapeutic areas in Novartis, including oncology, immunology, cardiovascular renal metabolism, neuroscience, and global health. This position drives close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), and Operations through PK science sub-teams to achieve a holistic and integrative perspective of the ADME/clinical pharmacology properties of candidates and drugs. Collaborates effectively with broader, cross‑disciplinary project teams to ensure PKS strategies are well integrated into project plans and scientific discussions. About the Role #LI_Hybrid Location: Basel, Switzerland Key responsibilities: • Represent the PK Sciences function in project teams, interactions with stakeholders within the organization and interactions with regulatory agencies, as appropriate • Proactively contributes to developing drug candidates across Research Development and Commercial continuum, providing expert pharmacokinetic / drug metabolism and clinical pharmacology input • Work with teams to elucidate the understanding of PK/PD relationships and develop dosing strategies and predictions • Develop and execute clinical pharmacology strategies, including input into nonclinical and clinical study design, and analyzing PK and PK/PD data, to support compound development from discovery through late development • Provide PK, dosage, and PK/PD components of study protocols, reports, project summaries and development plans, and author pharmacokinetic/clinical pharmacology/biopharmaceutics sections of IND/IMPDs and NDA/BLAs as well as prepare appropriate responses to Health Authority questions • Drive close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), through PK science sub-teams. • Works in close collaboration with clinicians and clinical development colleagues to integrate PKS insights into study design, data interpretation, and project decision‑making • Use of Artificial intelligence (AI) / Machine Learning (ML) approaches to enable model guided molecular design, preclinical and clinical data automation, authoring regulatory documents, and the use of predictive models This role reports to Therapeutic Area group in PK Sciences within Translational Medicine (TM) in Biomedical Research. PKS is a global organization situated within Translational Medicine (TM), the clinical research arm of Biomedical Research within Novartis. PK Sciences plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, bridging drug discovery and clinical application. PK Science is an enterprise-wide organization, working across both Biomedical Research and the Development organizations to advance the scientific knowledge of pharmacokinetics, metabolism and clinical pharmacology. Essential requirements: • Ph.D. / Pharm.D. with relevant experience in clinical pharmacology, drug metabolism and pharmacokinetics or a related background. • A minimum of 0-2 years of experience in drug discovery and/or development in a relevant environment (academia, CRO, biotech or Pharma). 2+ years of experience preferably in a lead role overseeing ADME/DMPK project strategy, either in discovery or clinical development to be considered for Principal Scientist II • Extensive and in-depth knowledge of pharmacokinetics including, drug metabolism and PK/PD evaluation, experience in working in project teams (preferably global) as well as sound awareness of recent developments in drug development and regulatory sciences. • Exposure to working in a cross-functional, matrixed, project-team environment. • Strong oral and written communication skills. Desirable Requirements: • Hands-on project experience with Artificial intelligence (AI) / Machine Learning (ML) approaches is a plus Leadership / Novartis Behaviors in Action • Delivers results through disciplined execution, continuous improvement, and a strong focus on value and outcomes. • Demonstrates an enterprise mindset and strong ownership by prioritizing resources and decisions for maximum Novartis and patient impact. • Role models Novartis leadership behaviors through visible actions, continuous self reflection, and openness to feedback • Builds trust through transparent communication, clear accountability, and consistent delivery against commitments. AI fluency: • Brings strong AI and digital fluency, using enterprise tools to enhance insight generation, decision making, and team productivity. **This is a dual level posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered. 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary We are seeking an enthusiastic and motivated PK Sciences project team representative to develop and implement translational or clinical pharmacology strategies to support the pursuit of transformative new medicines through late clinical development. Our unique organizational structure enables colleagues to work seamlessly in the translational and/or clinical space, offering opportunities for development and bench-to-bedside-to-bench translation. Experience in late discovery and/or clinical area is preferred. The scope of the role potentially includes small molecules, biologics/therapeutic proteins, antibody drug-conjugates, radioligand therapies and/or cell therapies across major therapeutic areas in Novartis, including oncology, immunology, cardiovascular renal metabolism, neuroscience, and global health. This position drives close interdisciplinary collaboration among the PK Science disciplines, Drug Disposition (ADME, BA), Modeling & Simulation (M&S), and Operations through PK science sub-teams to achieve a holistic and integrative perspective of the ADME/clinical pharmacology properties of candidates and drugs About the Role #LI_Hybrid Location: Basel, Switzerland Key Responsibilities: • Independently represent the PK Sciences function in cross-functional project teams, interactions with stakeholders within the organization and interactions with regulatory agencies, as appropriate • Lead a PK Science Subteam with interdisciplinary representation of the major functions from within PK Science and beyond • Ensures implementation of project strategies and monitors timelines, objectives, and budgets for assigned projects • Present projects at various institutional review and approval boards • Proactively contributes to developing drug candidates across Research Development and Commercial continuum, providing expert pharmacokinetic / drug metabolism and clinical pharmacology input • Develop and execute clinical pharmacology strategies, including input into nonclinical and clinical study design, and analyzing PK and PK/PD data, to support compound development from discovery through late development • Provide PK, dosage, PK/PD and M&S component of study protocols, reports, project summaries and development plans, and author pharmacokinetic/clinical pharmacology/biopharmaceutics sections/radiation dosimetry of IND/IMPDs and NDA/BLAs as well as prepare appropriate responses to global Health Authority questions • Use of Artificial intelligence (AI) / Machine Learning (ML) approaches to enable model guided molecular design, preclinical and clinical data automation, authoring regulatory documents, and the use of predictive models • Is a mentor to or manages junior associates in the organization This role reports to Therapeutic Area Head in PK Sciences within Translational Medicine (TM) in Biomedical Research. PKS is a global organization situated within Translational Medicine (TM), the clinical research arm of Biomedical Research within Novartis. PK Sciences plays a pivotal role in bringing innovative medicines to patients, by building on research advances to develop new therapies, bridging drug discovery and clinical application. PK Science is an enterprise-wide organization, working across both Biomedical Research and the Development organizations to advance the scientific knowledge of pharmacokinetics, metabolism and clinical pharmacology. Essential Requirements: • Ph.D. / Pharm.D. with relevant experience • Preferred candidates will have a minimum of 5+ yrs at the Senior Principal Scientist Level and 8+ years at the Associate Director level) in clinical pharmacology, drug metabolism and pharmacokinetics or a related background in an industry setting. • Extensive and in-depth knowledge of pharmacokinetics including, drug metabolism and PK/PD evaluation, experience in working in project teams (preferably global) as well as sound awareness of recent developments in drug development and regulatory sciences. • Demonstrated success in working in a cross-functional, matrixed, project-team environment. • An influential Team player and talented negotiator with strong oral and written communication skills. • Proven record of mentorship and/or people management Desirable Requirements: • Hands-on project experience with Artificial intelligence (AI) / Machine Learning (ML) approaches is a plus Leadership / Novartis Behaviors in Action • Delivers results through disciplined execution, continuous improvement, and a strong focus on value and outcomes. • Demonstrates an enterprise mindset and strong ownership by prioritizing resources and decisions for maximum Novartis and patient impact. • Role models Novartis leadership behaviors through visible actions, continuous self reflection, and openness to feedback • Builds trust through transparent communication, clear accountability, and consistent delivery against commitments. • Empowers others to innovate and improve while maintaining high scientific, ethical, and operational standards. AI fluency: • Brings strong AI and digital fluency, using enterprise tools to enhance insight generation, decision making, and team productivity. • Accountable for the ethical, transparent, and compliant use of AI in line with Novartis AI governance and data protection standards. External eminence: • Acts as an external thought leader, advancing Novartis’ reputation in translational science and innovation. Operational excellence: • Drives operational excellence through disciplined execution, continuous improvement, and effective use of resources to maximize PKS and enterprise value. • Acts as a responsible steward of people, data, and digital capabilities, leveraging AI and automation to improve efficiency, quality, and decision speed. *This is a dual level posting. The final level & title of the offer role would be determined by the hiring team based on the skills, experience & capabilities required to perform the role at the level the role has been offered. 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary Location: Basel, Switzerland #onsite Role Purpose: We are seeking a highly motivated Senior Expert Analytical Scientist with extensive experience in mass spectrometry to join our Analytical Research & Development (ARD) team. ARD is part of the Technical R&D Department within Development and plays a pivotal role in the characterization and analysis of Drug Substances and Drug Products throughout the transition from discovery to commercial production. About the Role Responsibilities include designing, executing, and planning scientific experiments, and reporting results in line with the ARD Oligonucleotides Analytics project. Ensure timely, high-quality delivery of supplies and knowledge generation. Lead, manage, and support project and team activities, contribute to analytical strategy, and promote scientific and operational excellence within the TRD-NCE goals. This role is part of the ARD Science & Operation - Oligonucleotides Analytics Team. Major accountabilities: Independently design, plan, execute, interpret, and report analytical activities for Oligonucleotides (DS and DP) utilizing cutting-edge analytical sciences and technologies (such as analytical method development, validation, transfer, stability, release testing, and formulation development analytics) in accordance with established timelines and quality standards. This position also requires active participation in laboratory operations. Develop and apply mass spectrometry methods for oligonucleotides. Foster and share best practices, provide robust scientific and technical expertise within the analytical project sub-team, among analytical scientists, and throughout the organization. Create analytical documents that align with global project strategies by phase. Assist in strategic planning, design, and execution. Participate to the planning and implementation of laboratory experiments for designated projects, including activity scheduling, experiment monitoring, and data analysis. Main contact for science and technical issues with internal stakeholders. Offer scientific guidance and mentorship to laboratory associates. Oversee technical analytical deviations and recommend appropriate corrective and preventive actions (CAPAs). Assist with audits and health authority inspections, making sure there are no major findings in the areas assigned. Follow SOPs, GMP, GLP, QM, HSE, ISRM, and Novartis Guidelines. Demonstrate excellent collaboration and encourage sharing of expertise. Minimum Requirements: PhD with a minimum of 3 years’s experience or Master degree in analytical chemistry with a minimum of 10 years’ experience in the pharmaceutical industry. Proficiency in using hyphenated analytical separation and detection techniques including mass spectrometry. Excellent knowledge of general laboratory management and analytical techniques. , e.g. HPLC, UV-spectrometry, titration. Proven experience in quality principles driving drug development such as GMP; understanding of general regulatory and quality expectations. Ability to perform in a highly dynamic environment Key qualities include strong coordination, clear communication, teamwork, self-motivation, and quick learning. 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 E-Mail schreiben 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 Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Summary The Head DCM leads the Design & Construction Management function, accountable for end to end governance, delivery, financial performance, and strategic development of all capital projects within the region. The Head DCM ensures Novartis can plan, design, authorize, execute, and govern major capital investments with transparency, compliance, and strategic alignment. About the Role Major Accountabilities but not limited to Lead the regional DCM team and govern third party service providers in DCM project management Oversee the entire capital appropriation request lifecycle, including ensuring high‑quality project options analysis, feasibility assessments, and scope validation, reviewing and approving ECAR/PCAR deliverables, financial assumptions, cost estimates, and risk assessments Ensuring compliance with local frameworks (e.g., Swiss SIA standards for CH). Financial Management & Savings Delivery accountable for annual capital spend of >100mUSD Spend Lead financial forecasting, cost controls, capitalization alignment, and savings commitments Act as senior interface to Real Estate Heads, Finance controllers, Procurement, HSE, Business units, External partners, authorities, and planners Demonstrate company values on a consistent basis Drive culture within organization that retains and develops talent to create a pipeline for organizational growth, as well as one which values diversity and embraces inclusive behaviors. Minimum Requirements Extensive experience in capital project management, engineering, construction, or real estate within regulated environments Deep knowledge of CAR/ECAR processes, financial modelling, cost control, and project governance structures Strong leadership capability in matrix organizations, navigating suppliers, authorities, and technical teams Understanding of local regulatory frameworks (e.g., Swiss SIA norms for CH, Knowledge of GxP standards) Strategic mindset with ability to lead organizational transformation (e.g., DCM carve‑outs, NOCC integration) Strong communication skills, both written and verbal Languages English/German 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) 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: Learn about all the ways we’ll help you thrive personally and professionally. Read our handbook (PDF 30 MB)

Job ID REQ-10074716 Mar 25, 2026 Switzerland Summary We offer two 6-month legal traineeship positions in Legal for Corporate Functions, one starting on January 1, 2027, and one starting on June 1, 2027! About the Role Are you interested in pursuing a career in law? We have the perfect opportunity for you! Our legal trainee position offers excellent hands-on, in-house legal experience within the dynamic and multinational environment of a leading pharmaceutical company. More than 70-000 unique individuals work at Novartis, all with different needs and aspirations, aligned to a single inspirational purpose: to Reimagine Medicine for millions of patients around the world. We are seeking a motivated and diligent legal trainee who has the courage to navigate in unknown and ambiguous legal areas and has the curiosity to learn and being exposed to interesting and challenging new legal questions. If you're passionate about making a difference and keen to kickstart your career with our in-house team, this could be the ideal role for you. We offer two 6-month legal traineeship positions in Legal for Corporate Functions, one starting on January 1, 2027, and one starting on June 1, 2027. Your responsibilities include: You'll be the backbone of our Legal team, offering essential advice in employment law (including questions related to Diversity, Equity & Inclusion), as well as litigation and investigation. You'll have the opportunity to tackle complex global and local issues, transforming challenges into solutions. You'll get your hands on practical tasks, managing individual legal cases, but also major projects (e.g. related to reorganizations, divestments, implementation of new policies and processes, artificial intelligence, etc.), drafting and reviewing agreements, internal regulations, and templates. This is your chance to shift from theory to practical application, making an immediate impact. Your role will involve in-depth legal research and the creation of legal memoranda, helping us to break down complex ideas into digestible insights. Here, your knowledge will fuel our mutual success. What you-ll bring to the role: Swiss Bachelor of Law (BLaw) und Master of Law (MLaw); master degree needs to be completed before start date Excellent proficiency in English and German, both in verbal and written communication High motivation and ability to work independently on challenging tasks and projects Prior legal internship and knowledge in employment law is a plus Are you ready to sharpen your skills and inspire change? If you're excited to contribute and learn, apply now, and submit a cover letter that includes your motivation for the position and your availability regarding the two traineeships (i.e. starting date January 1, 2027 or June 1, 2027). 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. 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: Learn about all the ways we-ll help you thrive personally and professionally. Read our handbook (PDF 30 MB) Division Legal Business Unit Legal Location Switzerland Site Basel (City) Company / Legal Entity C010 (FCRS = CH010) Novartis International AG Functional Area Others Job Type Full time Employment Type Early Career (Befristet) Shift Work No Others Legal Switzerland Job ID REQ-10074716 Legal Trainee - Novartis Corporate Functions Apply to Job (link is external)