The role involves participating in registration activities including reviewing and validating translations of SmPCs, labels, and patient information leaflets
Job Summary
The role involves participating in registration activities including reviewing and validating translations of SmPCs, labels, and patient information leaflets.
Candidates will coordinate regulatory submissions for clinical studies and in vitro medical devices with the ANSM and international teams.
Amgen offers a dynamic collaborative environment with daily mentorship from a Regulatory Manager to support professional development.
Matching Summary
The role involves participating in registration activities including reviewing and validating translations of SmPCs, labels, and patient information leaflets.
Skills & Requirements
Must-have
French language proficiency required
English reading and writing skills
Office software (Pack Office) familiarity
Nice-to-have
Strong communication and proactivity
Synthesis and analytical thinking
Collaborative team spirit
Key Requirements
Bac+6 Pharmacy degree in Regulatory Affairs or Health Law
Alternance contract availability starting September 2026
12-month internship duration commitment
Work Rights
Must have right to work in France for apprenticeship