CQV project manager
Job in
Raleigh, Wake County, North Carolina, 27601, USA
Listed on 2026-06-16
Listing for:
vTek Systems Inc
Full Time
position Listed on 2026-06-16
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Regulatory Compliance Specialist
Job Description & How to Apply Below
We are hiring a CQV Project Manager to lead commissioning, qualification, and validation projects within pharmaceutical and biotech manufacturing environments.
This role combines hands-on CQV knowledge with project leadership—owning validation execution, managing timelines, and ensuring systems are ready for GMP production.
Key Responsibilities- Lead CQV execution across equipment, utilities, and facility systems
- Oversee IQ/OQ/PQ planning, execution, and closeout
- Manage project schedules, milestones, and deliverables
- Drive startup, system turnover, and validation readiness activities
- Coordinate with engineering, QA, operations, and vendors
- Oversee validation documentation (protocols, reports, deviations, risk assessments)
- Identify risks and ensure projects stay on track
- 5–10+ years of experience in CQV, validation, or CQV project management
- Strong background in GMP environments + IQ/OQ/PQ
- Experience with:
- Utilities (WFI, clean steam, process gases)
- Facility systems (HVAC, clean rooms)
- Ability to lead on‑site CQV execution and cross‑functional teams
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