The intern will work on a wide variety of topics related to drug regulation within the French affiliate's regulatory team
Job Summary
The intern will work on a wide variety of topics related to drug regulation within the French affiliate's regulatory team.
Key activities include participating in the preparation and submission of MA variations, monitoring dossiers under evaluation, and controlling packaging artwork.
The role involves close collaboration with various departments and the European regulatory team, as well as participating in regulatory intelligence and departmental meetings.
Matching Summary
The intern will work on a wide variety of topics related to drug regulation within the French affiliate's regulatory team.
Skills & Requirements
Must-have
Regulatory Affairs France and Europe
Regulatory dossier preparation
Packaging artwork control
Regulatory intelligence
English proficiency
Nice-to-have
Analytical and synthesis skills
Team player
Open-minded and curious
Key Requirements
Master 2 in Regulatory Affairs/Registration
Knowledge of health authorities structure
Knowledge of pharmaceutical laboratory organization
Proficiency in Outlook, Word, Excel, PowerPoint, Internet