Opportunities · Internship
Regulatory Site Compliance Intern
Sanofi
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- When
- Summer 2027
- Where
- Marcy-l'Etoile, France
- Apply by
- Feb 8, 2027
What you'll do
- Participate in identifying relevant documents and scientific information required to support regulatory submissions
- Contribue to the analysis and synthesis of scientific data from various sources to support the preparation of robust and well-structured regulatory dossiers
- Support the coordination of regulatory writing activites to ensure alignement across contributors and adherence to timelines
- Take part in organizing meetings with subject matter experts to review, validate and aligne on scientific content and editorial choices
- Collaborate with the team to support the overall regulatory writing strategy within the department
- Help drafting responses to questions raised by health authorities to ensure accuray, consistency and regulatory compliance
What they want
- Soft and technical skills: autonmy, rigor, analytical mindset. Knowledge of regulatory affairs. Proficiency in Microsoft Office.
- Education: bac + 5 in pharmacy, life sciences or regulatory affairs
- Languages: English fluent
- Why choose us?
- Launch your career with a company that invests in you — and empowers you to reimagine what’s possible.
- Build your future with access to the latest tools, digital innovation, and continuous learning that keep you ahead of the curve.
Full posting
Job title: internship 6 months regulatory site compliance
- Location: Marcy L’Etoile
- Until: january 2027
About the job
As an intern within our Site Quality Operations teams, you’ll contribute to the preparation and maintenance of regulatory dossiers for vaccines. Ready to get started?
Ready to grow your skills while helping shape the future of healthcare? At Sanofi, you’ll be empowered to learn, ask questions, and bring your ideas to life – all while supported by inspiring mentors and collaborative teams.
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.
Main responsibilities
- Participate in identifying relevant documents and scientific information required to support regulatory submissions
- Contribue to the analysis and synthesis of scientific data from various sources to support the preparation of robust and well-structured regulatory dossiers
- Support the coordination of regulatory writing activites to ensure alignement across contributors and adherence to timelines
- Take part in organizing meetings with subject matter experts to review, validate and aligne on scientific content and editorial choices
- Collaborate with the team to support the overall regulatory writing strategy within the department
- Help drafting responses to questions raised by health authorities to ensure accuray, consistency and regulatory compliance
About you
- Soft and technical skills: autonmy, rigor, analytical mindset. Knowledge of regulatory affairs. Proficiency in Microsoft Office.
- Education: bac + 5 in pharmacy, life sciences or regulatory affairs
- Languages: English fluent
Why choose us?
- Launch your career with a company that invests in you — and empowers you to reimagine what’s possible.
- Build your future with access to the latest tools, digital innovation, and continuous learning that keep you ahead of the curve.
- Grow in a purpose-driven company where your voice matters and your work helps improve millions of lives.
- Thrive in inclusive, flexible workplaces that support your personal and professional well-being.
- An attractive internship bonus.
- Depending on your location, access to a company restaurant with a contribution from Sanofi.
- Our recruitment process is designed to be fast and efficient. If your application is accepted, you will receive a call from our recruiter for an initial telephone interview, followed by a quick meeting with the manager.
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.
Pursue progress, discover extraordinary
Better is out there. Better medications, better outcomes, better science. But 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. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com !
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Posted
Oct 8, 2026
Applications close
Feb 8, 2027
124 days left
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