You will join the Regulatory Affairs Department based at the French Headquarters in Puteaux – Paris La Défense
Job Summary
You will join the Regulatory Affairs Department based at the French Headquarters in Puteaux – Paris La Défense.
You will work on a range of products and participate in various regulatory activities throughout the drug lifecycle.
This role involves participating in the preparation and submission of variation dossiers for Marketing Authorizations and monitoring dossiers under evaluation by authorities.
Matching Summary
You will join the Regulatory Affairs Department based at the French Headquarters in Puteaux – Paris La Défense.
Skills & Requirements
Must-have
Regulatory Affairs France and Europe
Drug lifecycle regulatory activities
Submission dossier preparation
Authority evaluation monitoring
Nice-to-have
Open and curious mindset
Client-oriented internal results
Key Requirements
Master 2 in Regulatory Affairs / Registration
Scientific or Pharmacy background
Professional English proficiency
Proficiency in Outlook, Teams, Word, Excel, PowerPoint, Internet