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 suppor t: Assist the RA team with product life cycle submissions, including post‑approval variations, ensuring completeness and accuracy .Artwork revie w: Perform artwork proof‑reading prior to implementation to ensure regulatory conformity and version control .Project assistanc e: Contribute to product divestment activities (if applicable), following internal procedures and timelines .Document managemen t: Maintain and organize regulatory files (electronic and paper) for reliable tracking, retrieval, and archiving of controlled documents .Good Regulatory Practice (GRP ): Support GRP activities and routine compliance checks to align with internal SOPs and HSA expectations .Operations and admi n: Provide operational and administrative support for assigned RA projects and...