Sr. Validation Engineer

The Sr. Validation Engineer supports commissioning, qualification, and validation (CQV) activities for GMP manufacturing facilities, utilities, equipment, computerized systems, and manufacturing processes within a fast-paced CDMO environment. This role plays a key part in supporting multiple client programs across clinical and commercial manufacturing, ensuring compliance with cGMP, FDA, and EU GMP standards. The position involves developing and executing validation protocols, coordinating with cross-functional teams, and maintaining data integrity throughout the validation lifecycle.