Katalyst CRO is seeking a Quality Engineering and Validation Consultant to coordinate GMP activities for Cell & Gene Therapy operations. This onsite role reports to the GMP Quality group and supports clinical and commercial Drug Product manufacture.
The candidate will lead QA oversight of calibration programs, change controls, investigations and CAPAs, while collaborating across facilities, engineering, and analytical labs to ensure high-quality, compliant results.
#J-18808-LjbffrGMP Quality Engineer & Validation Consultant in boston at Unknown Company
This position is listed as full time and onsite.