About this role
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 @valspec.net. Any other domains are impersonations and should be ignored.
Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time.
Any third-party unsolicited resume submission(s) will immediately become the property of Valpro. Valpro will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.
Valpro is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.
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 @valspec.net. Any other domains are impersonations and should be ignored.
Candidates must be legally eligible to work in the United States without company sponsorship. Also, we are not interested in working on a corp-to-corp basis with other companies at this time.
Any third-party unsolicited resume submission(s) will immediately become the property of Valpro. Valpro will not pay any fee to a submitting employment agency, person, or entity unless a signed agreement is established.
Valpro is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to sex, race, color, religion, national origin, age, sexual orientation, gender identity, disability, protected veteran status or any other protected class. We are committed to providing a professional environment free of any discrimination or harassment, and we are proud to be a Drug-Free Workplace.
About Valpro Resourcing
Valpro Resourcing is hiring for the project manager – north carolina role. NewJob aggregates active openings directly from Valpro Resourcing's applicant tracking system, so this listing is current.
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