CQV Specialist I — Cell Therapy Manufacturing (Contract)
Legendcareers
Legend Biotech in New Jersey is seeking a CQV Specialist I (Contractor) for the Technical Operations team in Raritan. You will provide commissioning, qualification and validation support for the cell therapy manufacturing facility, ensuring cGMP compliance and data integrity across systems and equipment. The role requires a bachelor’s degree in science or engineering, at least four years of relevant experience, knowledge of cGMP/ICH, and proficiency with TrackWise, CMMS and Maximo. #J-18808-Ljbffr Legendcareers
Vacancy posted 4 days ago
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