Associate Director, Lead of Laboratory Compliance, Metrology, and Validation (m/f/d)

MSD Switzerland • ruswil, luzern • Posted July 08, 2026

About the Role

Associate Director – GxP Compliance and Documentation

The Pharmaceutical Analysis & Digital Technologies (PADT) department of our Company’s Research Laboratories Division is seeking applicants for an Associate Director position in the GxP compliance and documentation team to support the global analytical organization. The position will be based at the Schachen, Switzerland research facility.

Responsibilities

  • Manage a team of metrology and validation specialists supporting the maintenance and qualification of analytical equipment and instrumentation within the GMP environment.
  • Management and oversight of Good Manufacturing Practices (GMP) documentation, training, and standard operating procedures (SOPs) for the global network.
  • Originate and own investigations and change records related to laboratory instruments.
  • Drive harmonization of analytical procedures across the global network. Manage and contribute to SOPs relat...