CQV Engineer

About The Role:We are seeking a CQV Engineer to support commissioning, qualification, and validation activities within a pharmaceutical manufacturing environment. The ideal candidate will have experience supporting sterile and non-sterile equipment qualification projects and working closely with vendors and cross-functional teams. Responsibilities:• Support CQV activities for pharmaceutical manufacturing equipment• Perform temperature mapping and equipment qualification activities• Work with autoclaves, freezers, washers, and fillers• Write, review, and execute qualification protocols and documentation• Participate in vendor meetings and support project coordination• Ensure compliance with GMP and validation requirements Qualifications:• Experience in CQV within pharmaceutical or biotech environments• Strong knowledge of sterile & non-sterile processes• Hands-on experience with equipment qualification and temp mapping• Experience writing and reviewing validation protocols• Strong communication and documentation skills