CQV project manager
vTek Systems Inc
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 Requirements 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, cleanrooms) Ability to lead on‑site CQV execution and cross‑functional teams #J-18808-Ljbffr vTek Systems Inc
Vacancy posted 1 day ago
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