Validation Manager

This role oversees and manages all commissioning, qualification, and validation (CQV) processes for drug products, medical devices, and manufacturing processes at the Irvine site. The position is responsible for developing the site validation strategy, managing the Site Validation Master Plan, and leading cross-functional teams to ensure compliance with GMP regulations. The role also involves supervising validation activities, managing consultants, and representing the site during regulatory inspections and audits.