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.
Key responsibilities include participating in the preparation and submission of marketing authorization variation dossiers and tracking ongoing evaluations by ANSM and EMA.
The role requires close collaboration with pharmacists and regulatory managers to manage packaging modifications, RCP updates, and internal coordination processes.
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 or Pharmacy
Professional English proficiency required
Knowledge of French and European regulations
Nice-to-have
Strong analytical and synthesis skills
Excellent interpersonal relationship abilities
Curious and results-oriented mindset
Key Requirements
Student in Pharmacy or Scientific Master 2
Minimum 12-month contract duration
Proficiency in Outlook, Teams, Word, Excel, PowerPoint