Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
Cadre Assurance Qualité BPF
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.
About the Role
This position is responsible for implementing and monitoring the quality assurance system within the GMP Operations sectors of the Synthetics Scientific Platform and Quality Control in Montpellier, ensuring compliance with current regulatory standards including Good Manufacturing Practices (GMP).
Key Responsibilities:
Operational Quality Assurance
Represent Quality Assurance within:
- Analytical Sciences Department
- Physico-chemical laboratories (Quality Control)
- Pharmaceutical Sciences Department
Audit and approve:
- Manufacturing Masters and Technical Conditions
- Manufacturing batch records for GMP Operations sector
- Oversee bulk product manufacturing (primarily oral forms) conducted internally or externally
- Draft Quality Agreements for manufacturing subcontractors
- Participate in preparing regulatory authority inspections
- Coordinate and evaluate investigations following anomalies and/or process deviations
- Approve Change Controls in dedicated IT applications
- Draft, review and approve operating procedures
- Conduct self-inspections and external audits
- Deliver Quality training
- Initiate and/or participate in quality improvement projects
- Participate in lot recalls in collaboration with involved departments
QP Release
- Perform release of investigational medicinal products (bulk products)
Project Support
- Serve as Quality representative in CMC Synthetics project teams for assigned projects
About you
Qualifications:
Education
- Doctorate in Pharmacy required
Experience
Experience in pharmaceutical development and/or Quality Assurance, including:
- Operational Quality Assurance
- Project Quality representative
- Batch release
- CMC activity or CMC quality monitoring
Required Skills
- Mandatory Qualification: Doctor of Pharmacy degree
- Proficiency with IT tools
- Experience working in cross-functional projects or missions
- Fluency in both written and spoken English necessary for the role
Knowledge Areas
- Good understanding of GxP regulations
- Knowledge of Pharmaceutical Development processes
- Experience with subcontracting management
PursueProgress. Discover Extraordinary.
Progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. You can be one of those people. Chasing change, embracing new ideas and exploring all the opportunities we have to offer. Let’s pursue Progress. And let’s 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, or gender identity.
Watch our ALL IN videoand check out our Diversity Equity and Inclusion actions 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.
All-in on diversity
At Sanofi, diverse perspectives fuel the best solutions for patients. Hear from Monique Vessey, our Supply Chain Transformation Leader, on how her background shapes her approach to delivering life-changing medicines.
"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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