Pharma CQV Program Manager
Listed on 2026-10-13
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Pharmaceutical
Regulatory Compliance Specialist -
Management
Regulatory Compliance Specialist, Project & Program Management
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
The Pharma CQV Program Manager role at MMR Consulting is now open for applications in Greenville, SC, United States.
The advertised compensation is 120..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Pharma CQV Program Manager role in the description above.
We appreciate your interest in this position.
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