
Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
Cadre assurance quality - R&D CMC Synthetics
At a glance
Our teams produce and deliver over 4 billion units of medicines and vaccines every year, ensuring every breakthrough gets to the people who need it most.
Our state-of-the-art facilities, AI-powered smart factories, and cutting-edge automation are redefining what’s possible: ensuring treatments reach patients faster, safer, and more sustainably than ever before. This is where your skills, ambition, and passion can shape the future of healthcare.
Le contenu du poste est libellé en anglais car il nécessite de nombreuses interactions avec nos filiales à l’international, l'anglais étant la langue de travail.
This job offer is accessible to all, regardless of gender.
Job title:Cadre Assurance Quality - R&D CMC Synthetics
- Location: Sisteron, France
- Remote working: Up to 20% remote working possible
- Travel expected: 5-10%
About the job
Ready to shape the future of medicine? Join our R&D GQO team in Sisteron where we implement a quality management system adapted to early development phases. As a Cadre Assurance Quality - R&D CMC Synthetics, you'll make critical quality decisions based on scientific approach and rigorous risk assessment, balancing compliance requirements with necessary agility. Your expertise will be instrumental in ensuring our R&D CMC activities meet the highest quality standards while maintaining the flexibility needed for innovation.
About Sanofi:
We’re an R&D-driven, AI-powered biopharma company committed to improving people’s lives and delivering compelling growth. Our deep understanding of the immune system – and innovative pipeline – enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve people’s lives.
Key responsibilities:
- Manage Quality Assurance withint he R&D CMC Synthetics Sisteron
- Maintain R&D quality management system processes within &D CMC Synthetics scope (compliance with regulatory requirements and internal standards, quality procedures and documents, Conducts self-inspections and monitors corrective actions implementation)
- Coordinates investigations following deviations and non-conformities
- Manage Change control
- Review Clinical batch manufacturing records, Manufacturing Master Records or Technical Conditions
- Performs Quality Agreements for subcontractors; Manages supplier quality issues and monitors corrective actions; Conducts supplier audits
- Supervise analytical activities for R&D products: reviews and approves analytical methods and specifications; Participates in out-of-specification results and deviation investigations; Supports analytical method transfers
- Prepares and participates in internal and external audits or regulatory inspection preparation
- Conducts quality training
- Applies group HSE policy within scope of activity; Promotes HSE best practices
About you
Experience:
- 3-5 years experience in quality assurance in pharmaceutical industry, particularly in clinical API manufacturing
- In-depth knowledge of GxPs applicable to clinical API manufacturing and analysis
Education:
- Mastery of quality processes and continuous improvement tools
- Educational Background: Master's degree in scientific field (pharmacy or chemistry) or equivalent
Soft and technical skills:
- Knowledge of pharmaceutical regulations
- Analysis and problem-solving capability
- Strong communication and project management skills
- Rigor and organizational skills
- Ability to work in multidisciplinary teams
- Proficiency in quality IT tools
Languages:
- Good level of English (B2/C1)
Why choose us?
- Give life to science miracles as part of a forward-thinking, supportive team
- Discover countless opportunities to develop your talents and advance your career through promotion or cross-organizational assignments
- Benefit from a well-thought-out package of benefits that recognize your contribution and amplify your impact
- Take good care of yourself and your family with comprehensive health and wellness benefits, including high-quality healthcare, wellness programs, and parental leave of at least 14 weeks regardless of gender
- Play a key role in establishing best practices within our production unit
PursueProgress. 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
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.
Watch 'One day at Sanofi' and check out our Diversity Equity and Inclusion initiatives at sanofi.com
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Why work with us
- We’re problem-solvers and pioneers. United by the belief that everyone deserves a healthier future. We create best-in-class vaccines that prevent disease and protect lives.
- Innovation drives us. From AI and mRNA to next-gen science, we push the boundaries to deliver first- and best-in-class vaccines for infectious diseases worldwide.
- Growth happens here. With bold investments in R&D and world-class facilities, Sanofians across the entire vaccine lifecycle are shaping the future of global health.
- We do what’s right. Sustainability and DE&I drive our positive global impact—because the diverse communities Sanofians represent are the patients we serve.
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"Manufacturing and Supply is the bridge between the science that happens in research laboratories and the people and communities we serve."

Brendan O’Callaghan
Executive Vice President of Manufacturing and Supply
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