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

Profile

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.