CQV Lead, Capital Projects

Veg Group; North Carolina; On-site; USD 120,000 - 180,000; Full time

Job summary

Pinnaql seeks an experienced Commissioning, Qualification & Validation (CQV) Lead to support GMP-regulated biopharmaceutical capital projects in North Carolina. The ideal candidate will guide CQV activities from design through turnover, ensuring compliance with GMP requirements, and on-time delivery of qualification packages.

You will lead technical teams, manage schedules and vendors, review P&IDs and equipment specs, and collaborate across Engineering, QA, Manufacturing, and Operations to

Qualifications

• Bachelor's degree in Engineering, Life Sciences, or related technical discipline.
• 8–10+ years of experience in Commissioning, Qualification, and Validation within GMP-regulated pharmaceutical or biotechnology manufacturing.
• Demonstrated experience leading CQV execution for capital projects, including equipment installations, facility expansions, or manufacturing upgrades.
• Strong knowledge of FAT, SAT, IQ, OQ, PQ, and risk-based qualification methodologies.
• Experience qualifying manufacturing equipment, process systems, critical utilities, and facility infrastructure.
• Proven ability to lead technical teams, manage contractors, and coordinate multiple projects simultaneously.
• Knowledge of FDA regulations, cGMP requirements, and industry commissioning and qualification practices.
• Ability to work on-site in North Carolina.

Responsibilities

• Lead CQV activities for capital projects from design review through qualification, system turnover, and operational handover.
• Develop, review, and approve CQV plans, protocols, reports, risk assessments, and supporting documentation.
• Oversee commissioning and qualification of manufacturing equipment, process systems, clean utilities, and facility infrastructure.
• Coordinate and oversee FAT, SAT, IQ, OQ, and PQ activities, as applicable.
• Manage CQV execution schedules, deliverables, resources, and priorities to support capital project milestones.
• Provide technical leadership and direction to CQV engineers, validation specialists, contractors, and vendors.
• Collaborate with Capital Projects, Engineering, Automation, Quality Assurance, Manufacturing, and Operations.
• Review technical documentation, including P&IDs, equipment specifications, design drawings, and vendor documentation.
• Lead resolution of commissioning and qualification discrepancies, deviations, and change controls.
• Ensure CQV documentation meets GMP requirements, applicable regulatory standards, and established site procedures.
• Track project progress, identify risks, implement mitigation plans, and communicate status to stakeholders.
• Ensure timely completion of qualification packages, system turnover, and readiness for GMP operations.

Skills

CQV leadership

GMP compliance

Project management

Regulatory knowledge

Team leadership

Documentation

Education

Bachelor's degree in Engineering

Life Sciences background

Tools

P&ID reviews

Job description

Pinnaql is a trusted consulting partner to regulated life sciences companies, providing deep technical, validation, and quality expertise across every stage of the product lifecycle. We partner with pharmaceutical, biotech, and medical device organizations to navigate complexity, accelerate project timelines, and maintain a strong state of compliance and audit readiness.

We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:

Position Summary

Pinnaql is seeking an experienced Commissioning, Qualification & Validation (CQV) Lead to support capital projects at a GMP-regulated biopharmaceutical manufacturing facility in North Carolina.

The ideal candidate will have extensive experience leading CQV activities for capital equipment, manufacturing systems, utilities, and facility infrastructure, ensuring compliance with GMP requirements, project deliverables, and execution schedules.

Previous experience with capital projects, engineering standards, and CQV procedures is highly preferred.

Key Responsibilities

• Lead CQV activities for capital projects from design review and commissioning through qualification, system turnover, and operational handover.
• Develop, review, and approve CQV plans, protocols, reports, risk assessments, and supporting documentation.
• Oversee commissioning and qualification of manufacturing equipment, process systems, clean utilities, and facility infrastructure.
• Coordinate and oversee FAT, SAT, IQ, OQ, and PQ activities, as applicable.
• Manage CQV execution schedules, deliverables, resources, and priorities to support capital project milestones.
• Provide technical leadership and direction to CQV engineers, validation specialists, contractors, and vendors.
• Collaborate with Capital Projects, Engineering, Automation, Quality Assurance, Manufacturing, and Operations.
• Review technical documentation, including P&IDs, equipment specifications, design drawings, and vendor documentation.
• Lead resolution of commissioning and qualification discrepancies, deviations, and change controls.
• Ensure CQV documentation meets GMP requirements, applicable regulatory standards, and established site procedures.
• Track project progress, identify risks, implement mitigation plans, and communicate status to stakeholders.
• Ensure timely completion of qualification packages, system turnover, and readiness for GMP operations.

Required Qualifications

• Bachelor's degree in Engineering, Life Sciences, or a related technical discipline.
• 8–10+ years of experience in Commissioning, Qualification, and Validation within GMP-regulated pharmaceutical or biotechnology manufacturing.
• Demonstrated experience leading CQV execution for capital projects, including equipment installations, facility expansions, or manufacturing upgrades.
• Strong knowledge of FAT, SAT, IQ, OQ, PQ, and risk-based qualification methodologies.
• Experience qualifying manufacturing equipment, process systems, critical utilities, and facility infrastructure.
• Proven ability to lead technical teams, manage contractors, and coordinate multiple projects simultaneously.
• Knowledge of FDA regulations, cGMP requirements, and industry commissioning and qualification practices.
• Strong technical documentation, troubleshooting, communication, and stakeholder management skills.
• Ability to work on-site in North Carolina.

Preferred Qualifications

• Experience supporting large-scale biologics manufacturing or fill-finish operations.
• Experience with greenfield or brownfield capital projects.
• Familiarity with ASTM E2500, ISPE Baseline Guides, and risk-based commissioning and qualification approaches.
• Experience managing multidisciplinary CQV teams and external service providers.
• PMP certification or equivalent project leadership experience.

Ideal Candidate Profile

• A proactive, hands‑on CQV leader capable of independently managing commissioning and qualification workstreams, leading technical teams, resolving execution challenges, and ensuring capital projects meet quality, compliance, and schedule expectations.
• Candidates with previous Amgen experience and a proven track record delivering CQV activities for capital projects are strongly preferred.

At Pinnaql, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose‑driven, supportive team.

Pinnaql is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.