Knowledge of french and european regulatory affairs
You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the lifecycle of medicines
Job Summary
You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the lifecycle of medicines.
The role involves participating in the preparation and submission of marketing authorization variation dossiers and following up with health authorities like ANSM and EMA.
This is a 12-month minimum internship starting in September 2026, supervised by Célia CHIKHI.
Matching Summary
You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the lifecycle of medicines.
Skills & Requirements
Must-have
Master 2 in Regulatory Affairs or Pharmacy
Professional English proficiency written and oral
Knowledge of French and European regulatory affairs