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

Position Overview

The Pharmaceutical Analysis & Digital Technologies (PADT) department of our Company’s Research Laboratories Division is seeking an Associate Director for the GxP compliance and documentation team. The role will be based at the Schachen, Switzerland research facility and will drive a culture of quality and operational excellence across a global analytical network.

Key Responsibilities

• Manage a team of metrology and validation specialists supporting the maintenance and qualification of analytical equipment and instrumentation within the GMP environment.
• Oversee 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.
• Contribute to SOPs related to metrology and validation.