MMR Consulting is seeking a CQV Manager to lead commissioning, qualification, and validation activities for pharmaceutical manufacturing capital projects. You will oversee cross‑functional CQV execution across GMP facilities, utilities, equipment, automation, and processes while ensuring FDA and global regulatory compliance.
Travel to client sites throughout Raleigh, NC, will be required. The ideal candidate has 8+ years in pharma/biotech, 5+ years CQV PM experience in GMP environments, and
#J-18808-LjbffrPharma CQV Program Manager in greenville at Unknown Company
This position is listed as full time and onsite.