We are seeking a CQV Lead (OSD Manufacturing) with strong engineering fundamentals and hands-on experience in commissioning, qualification, and validation within a GMP-regulated Oral Solid Dose (OSD) environment. This role involves leading end-to-end CQV activities for manufacturing equipment, packaging systems, utilities, facilities, and computerized systems. The ideal candidate will combine deep technical expertise with a modern, digital-first approach to validation, ensuring systems are compliant, reliable, and inspection-ready. The CQV Lead will collaborate closely with cross-functional teams including QA, Automation, Engineering, and Manufacturing to deliver validated systems aligned with FDA, cGMP, and data integrity standards.

• Lead commissioning, qual...