CRISPR Therapeutics, Inc. is recruiting a Quality Site Head to oversee the Quality function at its internal manufacturing site. You will drive a culture of quality, oversee GMP-compliant operations, and prepare for Health Authority inspections to ensure product disposition and compliant manufacturing processes.
The role requires 15-20+ years in biopharma QA, deep regulatory knowledge, and a proven track record in leading high-performing QA teams in GMP environments. On-site presence in the U.S.
#J-18808-LjbffrQuality Site Leader — GMP & Compliance in framingham at Unknown Company
This position is listed as full time and onsite.