Sacramento, California
•
Yesterday
Onsite Role Position Summary The selected candidate will be responsible for commissioning, qualification, and validation activities related to GMP utilities, manufacturing equipment, process systems, and supporting infrastructure within a regulated biotech environment. The role requires strong expertise in qualification lifecycle management, GMP compliance, equipment validation, and cross-functional collaboration with Engineering, Manufacturing, Quality Assurance, and Validation teams. Key Resp
Easy Apply
Contract, Third Party
Depends on Experience
