Associate Director, Quality - Validation

The Associate Director, Quality - Validation leads a team to perform commissioning, qualification, and validation activities for GMP manufacturing facilities, utilities, equipment, and computerized systems within a fast-paced CDMO environment. This role supports multiple client programs across clinical and commercial manufacturing, ensuring compliance with cGMP, FDA, and EU GMP standards. The position involves cross-functional collaboration, managing validation documentation, and driving continuous improvement in validation processes.