Katalyst CRO in New Jersey seeks a senior CQV professional to support commissioning, qualification and validation for our cell therapy manufacturing plant, ensuring compliant operations and data integrity. You will lead CQV protocols, summary reports, CAPAs and investigations, mentor junior staff, and coordinate with QA, manufacturing and regulatory teams for audits and product release.
Candidates should have 8+ years of CQV experience in aseptic cell therapy environments, with strong
#J-18808-LjbffrCell Therapy CQV Engineer — GMP Validation Lead in raritan at Unknown Company
This position is listed as full time and onsite.