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Cqv Jobs in Raleigh, NC (NOW HIRING)

CRB

CQV Engineer III

Raleigh, NC · On-site

The CQV Engineer II will develop and implement commissioning strategies, lead verification activities, and manage deliverables in alignment with project timelines and quality standards. The position ...

Stellent IT LLC

CQV Lead, Upstream

Holly Springs, NC · On-site

$88K - $116K/yr

Title - CQV Lead, Upstream Location: Holly Springs, North Carolina Visa - OPEN NEED LEAD CANDIDATE ONLY WITH LINKEDIN PROFILE seeking a highly experienced CQV (Commissioning, Qualification, and ...

CRB

CQV Engineer III

Raleigh, NC

The CQV Engineer II will develop and implement commissioning strategies, lead verification activities, and manage deliverables in alignment with project timelines and quality standards. The position ...

Zifo

Principal CQV Consultant

Cary, NC · On-site

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / Pre‑Sales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight ...

Zifo

Principal CQV Consultant

Cary, NC · On-site

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / Pre-Sales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight to ...

Zifo

Principal CQV Consultant

Cary, NC · Hybrid

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / PreSales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight to ...

CAI

CQV Senior Project Manager

Raleigh, NC

$120K - $175K/yr

The CQV Senior Project Manager is responsible for leading services delivered to life sciences clients in all aspects of CQV-project execution and capital project Operational Readiness. Skills and ...

CAI

CQV Senior Project Manager

Raleigh, NC · On-site

The CQV Senior Project Manager is responsible for leading services delivered to life sciences clients in all aspects of CQV-project execution and capital project Operational Readiness. Skills and ...

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Cqv information

See Raleigh, NC salary details

$87.2K

$115K

$140.9K

How much do cqv jobs pay per year?

As of Aug 28, 2026, the average yearly pay for cqv in Raleigh, NC is $115,026.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,500.00 and $126,000.00 per year, depending on experience, location, and employer.

What is a CQV?

A CQV (Commissioning, Qualification, and Validation) job involves ensuring that equipment, systems, and processes in industries like pharmaceuticals and biotechnology meet regulatory and operational requirements. CQV professionals develop protocols, execute tests, and document compliance to ensure that facilities maintain safety and efficacy standards. They work closely with engineers, quality teams, and regulatory bodies to achieve validated systems.

What are the key skills and qualifications needed to thrive in the CQV position, and why are they important?

To thrive as a CQV (Commissioning, Qualification, and Validation) specialist, you need a strong background in engineering or life sciences, along with expertise in equipment qualification, validation protocols, and regulatory compliance. Familiarity with industry standards such as cGMP, FDA, and tools like validation software and document management systems is highly valuable. Strong analytical thinking, attention to detail, communication, and teamwork skills are crucial for ensuring project success and regulatory adherence. These skills ensure that pharmaceutical and biotech manufacturing processes meet rigorous quality standards and regulatory requirements.

What are the most common challenges faced by CQV specialists in the pharmaceutical industry?

CQV specialists in the pharmaceutical industry frequently encounter challenges such as managing tight project deadlines, adapting to evolving regulatory requirements, and coordinating across multi-disciplinary teams. Balancing compliance with operational efficiency demands a thorough understanding of documentation and attention to detail. Working with new or complex equipment can also present learning curves that require problem-solving and collaboration with engineering, production, and quality assurance teams. However, overcoming these challenges offers valuable experience and opportunities to build a robust skill set highly regarded in regulated industries.

What does a CQV engineer do?

A CQV (Commissioning, Qualification, and Validation) engineer is responsible for ensuring that manufacturing equipment, systems, and processes meet regulatory standards and quality requirements. They develop and execute validation protocols, perform testing, and document compliance to support product quality and safety in industries like pharmaceuticals and biotech.

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Cqv jobs near you
Infographic showing various Cqv job openings in Raleigh, NC as of August 2026, with employment types broken down into 89% Full Time, 3% Part Time, 5% Contract, and 3% Nights. Highlights an 91% Physical, 2% Hybrid, and 7% Remote job distribution, with an average salary of $115,026 per year, or $55.3 per hour.

CQV Engineer III

Raleigh, NC • On-site

CRB
Construction • 1 - 5K employees
Learn more about CRBexternal

Full-time

Re-posted 18 days ago

Job description

Company Description
CRB is a leading provider of sustainable Engineering, Architecture, Construction and Consulting solutions to the global life sciences and food and beverage industries. Our 1,200 employees provide best-in-class solutions that drive success and positive change for our clients, our people and our communities. CRB is a privately held company with a rich history of serving clients throughout the world, consistently striving for the highest standard of technical knowledge, creativity and execution.
Job Description
CRB is seeking a highly motivated and self-driven CQV Engineer III to support the delivery and execution of Commissioning, Qualification, and Validation (CQV) services across Life Sciences projects. The ideal candidate will provide technical leadership and field execution support for equipment and utility systems from design through facility turnover.
This role involves guiding internal and external CQV resources, coordinating with multi-disciplinary project teams, and ensuring compliance with client and global regulatory requirements. The CQV Engineer II will develop and implement commissioning strategies, lead verification activities, and manage deliverables in alignment with project timelines and quality standards.
The position requires excellent organization, communication, and leadership skills, as well as the ability to work collaboratively across engineering, QA, and construction teams in a dynamic project environment.
  • Define and document client requirements and develop project-specific CQV plans
  • Review and approve commissioning and qualification strategies for equipment and utilities
  • Provide input on operability, maintainability, and reliability considerations during design
  • Lead or support execution of commissioning, qualification, and validation activities
  • Witness and verify FAT/SAT, test protocols, and qualification execution
  • Provide independent verification and quality oversight of CQV deliverables
  • Act as the primary interface between CQV, engineering, and construction teams
  • Develop and manage CQV schedules, ensuring alignment with project milestones
  • Support risk assessments and ensure compliance with regulatory expectations
  • Mentor and train junior engineers and project team members on CQV best practices
  • Track, report, and communicate CQV progress and issues to project and regional leadership
  • Support lessons learned and continuous improvement initiatives within the CQV organization

Qualifications
  • Master's Degree in Engineering, Life Sciences, or related field with minimum 5 years of CQV experience, OR
  • Bachelor's Degree in Engineering, Architecture, or Construction Management with minimum 5+ years of CQV experience in the Life Sciences industry
  • Technical Experience:
  • Proven experience with commissioning and qualifications of life sciences equipment and utility systems (e.g., process equipment, clean utilities, HVAC, WFI, CIP/SIP, nitrogen, compressed air, etc.)
  • Working knowledge of cGMP, FDA, EU, and ISPE guidelines, including ISPE Baseline Guide 5 and Risk-Based Approach to Commissioning and Qualification
  • Familiarity with URS, FAT, SAT, IQ, OQ, PQ documentation and execution
  • Proficiency in risk assessment methodologies, root cause analysis, and continuous improvement tools

Skills & Attributes:
  • Strong interpersonal, communication, and presentation skills
  • Demonstrated leadership in coordinating cross-functional CQV efforts
  • Excellent technical writing and document review capability
  • Flexible and willing to travel as needed (50% or more)

Additional Information
All your information will be kept confidential according to EEO guidelines.
CRB is committed to hiring and retaining a diverse workforce. We are proud to be an Equal Opportunity Employer and it is our policy to provide equal opportunity to all people without regard to race, color, religion, national origin, ancestry, marital status, veteran status, age, disability, pregnancy, genetic information, citizenship status, sex, sexual orientation, gender identity or any other legally protected category. Employment is contingent on background screening.
CRB does not accept unsolicited resumes from search firms or agencies. Any resume submitted to any employee of CRB without a prior written search agreement will be considered unsolicited and the property of CRB. Please, no phone calls or emails.
CRB offers a complete and competitive benefit package designed to meet individual and family needs.
If you are unable to complete this application due to a disability, contact this employer to ask for an accommodation or an alternative application process.

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