You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the regulatory lifecycle of medicines
Job Summary
You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the regulatory 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 internship requires a student in Pharmacy or a scientific profile preparing for a Master 2 in Regulatory Affairs.
Matching Summary
You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to work on the regulatory lifecycle of medicines.
Skills & Requirements
Must-have
Master 2 degree in Regulatory Affairs
Professional English proficiency
Knowledge of French and European regulations
Familiarity with health authority structures
Proficiency in Office tools and databases
Nice-to-have
Strong analytical and synthesis skills
Excellent interpersonal abilities
Team-oriented mindset
Client-focused approach
Curiosity and openness to new tasks
Key Requirements
Enrolled in Pharmacy or Scientific Master 2 program
Minimum 12 months contract duration
No visa sponsorship available
Work Rights
Must be eligible to work in France (Internship status)