6-Month Regulatory Site Compliance Intern

Sanofi; Marcy-l'Étoile; On-site; EUR 10,000 - 15,000; Full time

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

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