Job description

Type of contract: Permanent contract

Mission: You are responsible for regulatory affairs in the pharmaceutical field / medical devices. In particular, you carry out one or more of these activities:

  • Preparation of specific regulatory applications (applications for clinical trials, temporary use authorization (ATU), import applications, etc.)
  • Release of batches
  • Preparation, validation and dissemination of the texts relating to packaging articles and product information
  • Drafting of the procedures inherent in the regulatory activity
  • Checking promotional items
  • Drafting of CE marking dossiers


Pharmacist or scientific training (Master level), you have a first experience in pharmaceutical or medical industry and especially in regulatory affairs.

For agap2, all talents count. If you have a disability, do not hesitate to ask us your questions and to apply.