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.
Your mission includes participating in the preparation and submission of marketing authorization variation dossiers and tracking ongoing evaluations by ANSM and EMA.
This 12-month apprenticeship starting in September 2026 offers a chance to collaborate with pharmacists and regulatory managers on packaging modifications and RCP updates.
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
Nice-to-have
Strong analytical and synthesis skills
Excellent interpersonal and teamwork abilities
Curiosity and results-oriented mindset
Key Requirements
Student in Pharmacy or Scientific profile preparing Master 2
Minimum 12 months duration commitment
Proficiency in Outlook, Teams, Word, Excel, PowerPoint