Manufacturing and Supply
Where the
miracles of
science are made
a reality for patients
Regulatory Site Officer - all genders - Fixed-term contract until 26.02.2027
Frankfurt am Main, Germany
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.
About the job
External Manufacturing and Supply Large Molecule Specialty Care (EM&S LM SC) is responsible for GxP oversight of Contract Manufacturing Organizations (CMOs), Contract Laboratory Operations (CLOs), Distribution Centers and business partners involved in the manufacture, testing, storage and transport of Sanofi products. EM&S LM SC staff interact with functional units within other Sanofi sites, and other organizations within the External Manufacturing and Supply and Specialty Care network (e.g. procurement, supply chain, finance) to ensure compliance with internal and regulatory requirements, and to disposition intermediates (e.g. API, drug substance) and finished products with minimal risk to quality or product supply.
EM&S LM SC has responsibility for CMO and CLO and distribution activities related to products treating Rare Diseases and Rare Blood Disorders, Multiple Sclerosis (MS), and Oncology.
EM&S LM SC has offices based in Northborough and Cambridge, MA US; Frankfurt Germany; Ghent and Geel, Belgium and Amsterdam, the Netherlands
Main responsibilities:
This function can also support to other EM&S entities than EM&S LM SC.
Acts as a local regulatory interface between the external and internal manufacturing sites, quality units, MSAT, Global Regulatory Affairs and Sanofi affiliates
Collaborates closely with EM&S LM SC personnel in order to ensure compliant manufacturing and release operations
Manages and reviews CMC (Chemistry, Manufacturing and Controls) dossiers, variations, renewals, annual reports, site registrations and territory extensions as part of regulatory product lifecycle management responsibility
Reviews and approves cGMP or regulatory reports / change controls / protocols/ submissions and associated action plans in order to ensure regulatory and cGMP compliance
Analyses complex regulatory issues and processes, supports to build regulatory strategic plans and applies own professional knowledge to identify key areas of risk to compliance with registered details
Acts as a source of regulatory expertise for others and gives advice on own area to other functions and employees
Supports and ensures GMP and regulatory compliance and inspection readiness for products under ownership of EM&S LM SC
Supports dossier Compliance program in compliance to Sanofi Global Procedures.
Support for Deviation and CAPA
Additional Responsibilities
Support the Qualified Person in any GMP and regulatory aspects related to batch release of product, as applicable
May support internal regulatory assessment of information to support internal or external audits and supplier qualification as required
Support CMO compliance via GxP and regulatory documentation review and on-site visits/Person in Plant/audits if applicable.
Frequent inter-departmental, inter-organizational and external interactions
Support the development and management of quality agreements between Sanofi and the contractor
Support program for maintaining performance metrics
About you
Education
Bachelor’s degree with scientific background or equivalent and 5+ years of experience in a GxP or regulatory affairs environment. OR
Master’s degree with scientific background and 3 years of experience in a GxP or regulatory affairs environment
Experience
A working knowledge of conventional and biotechnological and small molecule manufacturing operations, aseptic processing, validation principles, quality control techniques and testing methodologies of drug substances and drug products is beneficial.
Experience within EM&S environment and/or as regulatory compliance responsible is an asset.
Knowledge and experience with regulatory database system (Veeva RIM) is an asset.
Soft and technical skills:
Good understanding of quality and regulatory systems and management tools.
Knowledge and experience of EU/US GMPs for the biotech/pharmaceutical industry, with an understanding of worldwide regulatory affairs.
Demonstrated ability to perform work that consistently requires independent decision making and the exercise of independent judgment and discretion.
Problem solving and technical writing skills.
Ability to multitask effectively
Willingness to travel
Languages: Good written and verbal communication in English
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.
Benefit from a well-thought-out benefits package that rewards your contribution and commitment.
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. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
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. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!
nullPursue 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
Find out more about this location
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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