The intern will work on a wide variety of topics related to drug regulation within the French subsidiary's regulatory team
Job Summary
The intern will work on a wide variety of topics related to drug regulation within the French subsidiary's regulatory team.
Key activities include participating in the preparation and submission of MA variations, monitoring ongoing dossiers with authorities, and regulatory control of packaging materials.
The role involves close collaboration with various departments such as pharmacovigilance, medical information, quality, and supply chain, as well as the European regulatory team.
Matching Summary
The intern will work on a wide variety of topics related to drug regulation within the French subsidiary's regulatory team.
Skills & Requirements
Must-have
Regulatory Affairs France and Europe
ANSM and EMA authorities
Regulatory monitoring of packaging
Regulatory watch national and European
English (oral and written)
Nice-to-have
Good analytical and synthesis skills
Sociable, good contact and team spirit
Open and curious
Proactive and process-oriented
Key Requirements
Master 2 in Regulatory Affairs / Registration
Knowledge of health authorities structure
Knowledge of pharmaceutical laboratory organization