Valspec
Life Sciences
CQVProjectManager–LifeSciences
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optimal for Manager candidates.
“CQV Project Manager – Life Sciences at Valspec. 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, CSV exposure, MES exposure, Automation systems exposure
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
Coordinate with engineering
Coordinate with operations
Coordinate with vendors
Oversee validation documentation
How You'll Work.
Team & Collaboration
Cross-functional teams
Process & Methodology
Project leadership, Schedule management, Milestone management, Deliverable management
Full Job Description
Valspec—a global provider of system validation and lifecycle services—provides commissioning and qualification of computerized systems for clients in the Life Sciences industry. Established in 1999, Valspec’s mission is to provide a wide spectrum of services that help its clients meet their capital project and lifecycle maintenance goals. Valspec’s projects are critical to the industry, and to the people who rely on its products. Many projects ensure that life-changing drugs are available to those who need them; others streamline production to meet demand at a lower cost, allowing for the discovery of new and innovative therapies. 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 e
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