Job Description
Join our Regulatory Affairs team for an internship that provides structured exposure to the regulatory management of therapeutic products across their lifecycle. In this role,
What you’ll d
- oDossier preparation support: Assist the RA team with product life cycle submissions, including post‑approval variations, ensuring completeness and accuracy
- .Artwork review: Perform artwork proof‑reading prior to implementation to ensure regulatory conformity and version control
- .Project assistance: Contribute to product divestment activities (if applicable), following internal procedures and timelines
- .Document management: Maintain and organize regulatory files (electronic and paper) for reliable tracking, retrieval, and archiving of controlled documents
- .Good Regulatory Practice (GRP): Support GRP activiti...