On-Site Senior CQV Engineer — GMP Validation Lead
Visium Resources, Inc.
Visium Resources, Inc. seeks an experienced Senior CQV Engineer to lead commissioning, qualification, and validation activities for pharmaceutical and biotechnology facilities in Raleigh, NC. The role involves hands-on CQV work across process equipment, utilities, HVAC, cleanrooms, and automation systems, with cross-functional collaboration to ensure regulatory readiness. The ideal candidate has 5–10+ years in CQV/validation within GMP environments, strong knowledge of cGMP, FDA validation, and #J-18808-Ljbffr Visium Resources, Inc.
Vacancy posted 3 days ago
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