GMP Quality Lead — Deviations, CAPAs & Change Control

CSL is seeking a Senior Quality Associate in Bern, Switzerland, responsible for managing deviations, investigations, and change controls within the Clinical Development portfolio. This role ensures compliance with GMP regulations while providing support across Technical Product Development.

The ideal candidate will have a degree in a biological science and at least 3 years of experience in GMP manufacturing, Quality Assurance, or Regulatory Affairs.