You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to support the regulatory lifecycle of medicines
Job Summary
You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to support the regulatory lifecycle of medicines.
Key responsibilities include participating in the preparation and submission of marketing authorization variation dossiers and tracking files with health authorities like ANSM and EMA.
The role requires close collaboration with pharmacists and regulatory managers while ensuring strict adherence to timelines and internal processes.
Matching Summary
You will join the Regulatory Affairs Department at the France Headquarters in Puteaux to support the regulatory lifecycle of medicines.
Skills & Requirements
Must-have
Master 2 degree in Regulatory Affairs
Professional English proficiency
Knowledge of French and European regulations
Nice-to-have
Strong analytical and synthesis skills
Excellent interpersonal abilities
Results-oriented mindset
Key Requirements
Student in Pharmacy or Scientific Master 2
Minimum 12-month internship duration
Proficiency in Outlook, Teams, Word, Excel, PowerPoint