internship 6 months regulatory site compliance

Sanofi

Marcy-l'Étoile

On-site

EUR 10,000 - 15,000

Full time

5 days ago
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Benefits offered by this job

Internship bonus
Company restaurant access
Fast recruitment process

Job summary

Sanofi in Marcy L’Etoile is offering a 6-month internship within Site Quality Operations to contribute to preparing and maintaining regulatory dossiers for vaccines. You will gain hands-on experience in regulatory submissions and collaborate across teams under the guidance of mentors.

The role requires bac+5 in pharmacy or life sciences, fluent English, and a proactive, rigorous approach. You’ll develop skills in regulatory writing, data synthesis, and project coordination while working in a

Qualifications

  • Enrolment in bac+5 in pharmacy, life sciences or regulatory affairs.
  • Fluent English; knowledge of regulatory affairs.

Responsibilities

  • Identify documents for regulatory submissions.
  • Assist analysis and synthesis of scientific data for dossiers.
  • Support coordination of regulatory writing to meet timelines.
  • Organize meetings with experts to align content and editorial choices.
  • Support regulatory writing strategy within the department.
  • Draft responses to health authorities ensuring accuracy and compliance.

Skills

Autonomy
Rigor
Analytical mindset
Regulatory affairs knowledge
MS Office

Education

Bac+5 in pharmacy, life sciences or regulatory affairs

Tools

Microsoft Office

Job description

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
  • Participatein 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.

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