Job Description

MSD Switzerland is seeking an Associate Director for GxP Compliance and Documentation to oversee Quality Assurance for laboratory functions. In this role, you will manage a team dedicated to maintaining compliance standards, documentation, and SOPs within the GMP environment.

The ideal candidate will have at least 5 years of experience in the pharmaceutical industry, proven leadership skills, and the ability to effectively communicate in a multidisciplinary team setting. This full-time position is based in Luzern, Switzerland.

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