JobDiva, Inc. is seeking a CQV Specialist to lead commissioning, qualification, and validation activities for facility, equipment, and computerized systems supporting GMP cell therapy manufacturing.
This role owns qualification strategy and execution, ensuring compliant, risk-based validation aligned with USP <1058>, GAMP 5, and industry best practices. You will drive execution, manage deviations, and represent CQV in inspections.
#J-18808-LjbffrSenior CQV Specialist for GMP Cell Therapy Validation in new york at Unknown Company
This position is listed as full time and onsite.