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.
The role involves collaborating with pharmacists to prepare and submit variation dossiers for marketing authorizations while tracking evaluations by ANSM and EMA.
Candidates must demonstrate rigor, organization, and a results-oriented approach within a team environment.
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 in Regulatory Affairs
Professional English proficiency
Knowledge of French and European regulations
Nice-to-have
Strong analytical and synthesis skills
Excellent organizational abilities
Teamwork and relationship building
Key Requirements
Student in Pharmacy or Scientific Master 2
Minimum 12-month contract duration
Proficiency in Outlook, Teams, Word, Excel, PowerPoint