R&D
Là où votre curiosité fait avancer les miracles de la science
Senior Capability Analyst
Marcy-l'Étoile, France Salary Range EUR 54,400.00 - 72,533.33
En bref
Mettez votre curiosité au service d’une équipe où l’immunoscience de pointe rencontre l’innovation la plus avancée. Dans les domaines de l’oncologie, des maladies rares, de la neurologie et des vaccins, vous travaillerez à l’intersection entre la recherche en laboratoire et la découverte boostée par l’IA, tout en collaborant au-delà des frontières pour transformer des idées novatrices en impacts concrets. Que vous souhaitiez approfondir votre expertise scientifique ou évoluer en tant que leader, vous trouverez ici l’opportunité de le faire.
Global Regulatory Operations - Regulatory Digital Data & AI
Job title: Senior Capability Analyst
• Grade: 3.1
• Location: Gentilly, FR
• Job type: Permanent, Full time
About Sanofi
At Sanofi, we chase the miracles of science to improve people's lives. We are committed to transforming the practice of medicine through scientific breakthroughs that benefit society. Our Regulatory Affairs function plays a critical role in this mission, ensuring that our innovations reach patients safely and efficiently.
Our Team:
GRO Regulatory Data Digital & AI enables GRA to be a digital savvy and agile organization by fostering innovation, maximizing value, and driving simplification across process, data, and digital. As a key component of Sanofi's global regulatory strategy, we ensure that regulatory information is managed efficiently and effectively throughout the product lifecycle. The team are change agents that engage across GRA, partnering functions and external partners to enhance GRA's capabilities.
About the job
Sanofi is committed to creating an inclusive workplace that embraces diversity of thought, background, and experience. We believe that a diverse team strengthens our ability to innovate and better serve our patients worldwide.
Main responsibilities:
This role drives strategic execution and transformation of regulatory content management by leading compliance initiatives, enhancing user experience, and promoting process consistency—while actively driving innovation, digital transformation, and operational excellence. As a Senior Capability Analyst, you will lead development and execution of capability roadmaps within your domain, serve as a key bridge between regulatory subject matter experts, business process owners, and digital product teams, and develop scalable and compliant solutions.
Key responsibilities include:
• Lead development and execution of capability roadmaps within domain
• Design and optimize process and information architecture, balancing standardization and innovation needs
• Lead workshops, design sessions, and business testing activities to support solution development and validation
• Establish compliance frameworks and audit protocols by maintaining accurate records and documentation
• Conduct comprehensive analysis and translate into business solutions
• Develop and implement process improvements with measurable impact across end-to-end regulatory capabilities
• Lead preparation for audits and inspections for the capability
• Work with Digital Product Owners, Business Process Owners, and SMEs to drive capability adoption
• Drive capability adoption and change management strategies with the Training/Development and Communication teams
• Research and recommend emerging technologies and trends in regulatory capability development, digital adoption, and AI in life sciences
• Mentor junior team members
• Uphold Sanofi's Code of Ethics and integrity standards in all activities, ensuring compliance with global and local regulatory requirements and company policies
Team scope specific:
• Focuses on the end-to-end management of documents intended for submission, submission data, publishing activities, and content planning across the application lifecycle. This includes the orchestration of structured and unstructured content required for global regulatory submissions, ensuring consistency, traceability, and compliance. The team enables strategic capacity for content planning and execution of submission content, supporting timely and high-quality regulatory interactions.
• Publishing activities encompass the preparation, validation, and dispatch of regulatory submissions to health authorities, ensuring alignment with regional requirements and technical standards. The team ensures that publishing processes are integrated with content and data management workflows, enabling efficient and compliant submission delivery.
• Operating within the GxP-regulated environment for GRA Applications, the team acts as the Business System Owner (BSO) under the Agile framework. It ensures robust governance, alignment with regulatory requirements, and continuous improvement of processes and tools related to document, content, and publishing management. This capability also supports lifecycle management of regulatory applications
About you
• Experience:
• Grade 3.1: 5-7 years with demonstrated expertise in regulatory operations
• Soft Skills:
• Advanced communication and collaboration skills within a matrixed organization
• Ability to lead and influence in a fast-paced, cross-functional environment
• Technical skills:
• Advanced knowledge of document management systems and submission processes and RIM systems (experience with Veeva Vault, IDMP standards, or similar platforms is required)
• Expert understanding in business process analysis in regulatory affairs
• Advanced understanding of capability-based planning, agile delivery, or digital product lifecycles
• Proficiency with digital tools, automation, or AI
• Education:
• Grade 3.1: Bachelor's degree required, Master's preferred
• Languages: Fluent in English, both spoken and written
• Certifications:
• Grade 3.1: LEAN, Agile, BPMN or equivalent certifications preferred
-------------------------------------------------------------------------------------------------------------------------
Skills:
Technical Functional Transversal Other
International
Regulatory
Compliance
(Experienced),
Business Technology
(Advanced),
Artificial Intelligence
(AI) (Advanced),
Digital Adoption
(Advanced) Technology
Implementations
(Advanced),
Project Management
(Advanced),
Operational
Efficiency
(Experienced), Data
Analytics
(Experienced),
Design Thinking
(Advanced) Cross-Functional
Teamwork
(Experienced) Stakeholder
Relationship
Management
(Experienced)
About you
Experience:
- 7-10 years with demonstrated leadership in regulatory operations
Soft Skills:
- Expert communication and collaboration skills within a matrixed organization
- Ability to lead, influence, and drive change in a fast-paced, cross-functional environment
Technical skills:
- Expert knowledge of document management systems and submission processes and RIM systems (experience with Veeva Vault, IDMP standards, or similar platforms is required)
- Recognized authority in business process optimization in regulatory affairs
- Expert understanding of capability-based planning, agile delivery, or digital product lifecycles
- Strategic vision for digital tools, automation, or AI implementation
Education:
- Master's preferred plus specialized training
Languages:
- Fluent in English, both spoken and written
Certifications:
- Advanced certifications plus demonstrated application in LEAN, Agile, BPMN or equivalent
Why choose us?
- Bring the miracles of science to life alongside a supportive, future-focused team
- Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or lateral move, at home or internationally
- Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact
- Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high-quality healthcare, prevention and wellness programs and at least 14 weeks’ gender-neutral parental leave
Pursue Progress. Discover Extraordinary.
Join Sanofi and step into a new era of science - where your growth can be just as transformative as the work we do. We invest in you to reach further, think faster, and do what’s never-been-done-before. You’ll help push boundaries, challenge convention, and build smarter solutions that reach the communities we serve. Ready to chase the miracles of science and improve people’s lives? Let’s Pursue Progress and Discover Extraordinary – together.
At Sanofi, we provide equal opportunities to all regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity, protected veteran status or other characteristics protected by law.
#LI-FRA
#LI-Hybrid
Toujours Progresser. Découvrir l’Extraordinaire.
Rejoignez Sanofi et entrez dans une nouvelle ère de la science – où votre parcours peut être aussi transformateur que le travail que nous accomplissons. Nous investissons en vous pour que vous alliez plus loin, accélériez votre réflexion et accomplissiez ce qui n’a jamais été fait auparavant. Vous contribuerez à repousser les limites, à bousculer les conventions et à concevoir des solutions plus intelligentes pour les communautés que nous servons. Prêt·e à poursuivre les miracles de la science et à améliorer la vie des gens ? Poursuivons le progrès et découvrons l’extraordinaire – ensemble.
Chez Sanofi, nous croyons dans l’égalité des chances, sans distinction de race, de couleur, d’ascendance, de religion, de sexe, d’origine, d’orientation sexuelle, d’âge, de citoyenneté, d’état civil, de handicap, d’identité de genre ou de tout autre critère protégé par la loi.
La rémunération finale sera déterminée en fonction de l'expérience démontrée, des compétences, et autres facteurs objectifs. Les employés seront également éligibles aux programmes d'avantages sociaux de l'entreprise.
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sur ce site
Pourquoi nous rejoindre ?
- Élargissez vos horizons. Grandissez grâce à votre curiosité, avec le soutien nécessaire pour évoluer, apprendre et progresser dans une culture qui valorise le mentorat, la mobilité et le développement ambitieux.
- Accélérez les résultats grâce à la technologie. Exploitez la puissance de l'IA et de l'automatisation pour repousser les frontières de la science et réinventer ce qui est possible en matière de découverte de médicaments.
- Agissez grâce à une innovation inclusive. Contribuez à une science meilleure et à des résultats plus équitables en favorisant une recherche inclusive qui touche plus de personnes, de manière plus significative.
- Transformez les besoins des patients en avancées scientifiques. Faites naître des percées scientifiques qui partent des besoins des patients, et aboutissent à des traitements qui changent des vies.
Rencontrez Nils Libert, Associate Scientist
Faites la connaissance de Nils Libert, Associate Scientist en Belgique, où il joue un rôle clé dans l’avancement de recherches de pointe. Découvrez comment son travail contribue à faire progresser l’innovation, à ouvrir de nouvelles perspectives scientifiques et à développer des traitements qui changent la vie des patients partout dans le monde.
"Chez Sanofi, nous construisons un véritable accélérateur de R&D alimenté par la science la plus performante, l’innovation digitale et la volonté de transformer la vie des patients dans le monde entier."
Houman Ashrafian
Vice-Président Exécutif & Responsable R&D
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Nos domaines de recherche prioritaires
Découvrez comment nous réinventons l’avenir de la médecine grâce à l'immunologie, ouvrant la voie à des avancées transversales audacieuses, encore inimaginables il y a dix ans.
Rencontrez nos équipes dans les laboratoires
Poussez les portes de nos labos et écoutez les témoignages scientifiques qui transforment une science de pointe en impact réel, guidés par la curiosité, la collaboration et le sens du collectif.
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de talents
Que pourrions-nous accomplir ensemble ? Chaque Sanofien travaille sur des projets qui ont un véritable impact sur la vie des gens.
Inscrivez-vous dès aujourd'hui et découvrez nos dernières opportunités dès qu'elles seront disponibles.