Regulatory Affairs Postgraduate Program Switzerland

The Regulatory Affairs Postgraduate Training Program provides an immersive 2‑year training experience across two rotational assignments that cover Regulatory Affairs and Regulatory Chemistry, Manufacturing and Controls. The program offers 1year rotations in two distinct RA functions, starting in January2027.

Responsibilities

• Interact with global interdisciplinary project teams to provide strategic regulatory input on development, submission planning, documentation requirements, timelines, and strategic risks.
• Prepare high‑quality dossiers, drug substance and drug product quality documentation to support global regulatory submissions (e.g., Clinical Trial Applications, Market Authorization Applications, post‑approval variations).
• Adapt dossiers to specific national and regional regulatory requirements.
• Support submission and response activities, including planning, preparation, review, coordination, and submission.
• Ensure re...