You will work on a range of products and participate in various regulatory activities throughout the drug lifecycle
Job Summary
You will work on a range of products and participate in various regulatory activities throughout the drug lifecycle.
You will participate in the preparation and submission of MA variations, monitor ongoing evaluations by authorities (ANSM and EMA), and manage packaging modifications, RCPs, and legal notices.
This role is for a student in Pharmacy or a scientific Master 2 program with a focus on Regulatory Affairs/Registration, starting in September 2026.
Matching Summary
You will work on a range of products and participate in various regulatory activities throughout the drug lifecycle.