Valpro
Life Sciences
CQVProjectManager–LifeSciences
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“CQV Project Manager – Life Sciences at Valpro. Skills: CQV Project Management, GMP Environments, Validation Execution. Lead CQV execution. Oversee IQ/OQ/PQ planning”
What You'll Achieve.
Ensure systems are ready for GMP production
Industry & Context.
Risk identification
What They're Looking For.
Must Have
5-10+ years of experience in CQV, Validation or CQV project management background, Experience in GMP environments, IQ/OQ/PQ experience, Ability to lead on-site CQV execution, Ability to lead cross-functional teams
Nice to Have
Startup experience, Large capital project experience, Exposure to CSV, Exposure to MES, Exposure to automation systems
What You'll Do.
Oversee IQ/OQ/PQ planning
Oversee IQ/OQ/PQ execution
Oversee IQ/OQ/PQ closeout
Manage project schedules
Manage project milestones
Manage project deliverables
Drive startup activities
Drive system turnover
Drive validation readiness activities
Coordinate with engineering
Coordinate with operations
Coordinate with vendors
Oversee validation documentation
Identify project risks
Ensure projects stay on track
How You'll Work.
Team & Collaboration
Cross-functional teams
Process & Methodology
Project management, Timeline management, Milestone management, Deliverable management
Full Job Description
Valpro has several available opportunities supporting our world-class client sites or partner organizations. Whether you are an independent consultant or a potential employee looking for your next project, learn more about what we have to offer. View our open positions below. CQV Project Manager – Life Sciences (NC) 📍 Raleigh–Durham, NC About the Role 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: Process equipment (CIP/SIP, fill/finish, upstream/downstream, etc.) Utilities (WFI, clean steam, process gases) Facility systems (HVAC, cleanrooms) Ability to lead on-site CQV execution and cross-functional teams Nice to Have Startup or large capital project experience Exposure to CSV, MES, or automation systems Apply today to learn more about this exciting new life sciences project management opportunity! Valpro offers flexible career options that includes benefits such as paid time off, paid holidays, medical, 401K match, and other unique incentives. When receiving e-mails from a Proconex or Valspec recruiter, you will only receive e-mails from addresses ending in @proconexdirect.com, @proconex.net or @
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