MMR Consulting is seeking a Lead CQV Specialist to validate upstream/downstream bioprocess systems and process equipment in pharma/biotech settings. The role requires leadership to guide intermediate and junior specialists, and will involve working at client facilities in the Raleigh-Durham-Chapel Hill region.
Responsibilities include steering commissioning/qualification across DQ to PQ, developing PVPs, coordinating with cross-functional teams, and mentoring a team of validation staff.
#J-18808-LjbffrLead CQV Specialist - Biopharma Systems Validation in nc at Unknown Company
This position is listed as full time and onsite.