Knowledge of french and european regulatory affairs
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 files with health authorities.
This 12-month apprenticeship requires close collaboration with pharmacists and regulatory managers to manage packaging modifications and update product information.
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 written and oral
Knowledge of French and European regulatory affairs
Nice-to-have
Rigorous organizational skills
Strong analytical and synthesis abilities
Excellent interpersonal and team collaboration skills
Key Requirements
Student in Pharmacy or Scientific Master 2 degree
Minimum 12 months contract duration
Proficiency in Outlook, Teams, Word, Excel, PowerPoint