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Cqv Jobs in Raleigh, NC (NOW HIRING)

CQV Engineer Location: Holly Springs, NC Duration: Long-Term Contract Summary: We are hiring experienced CQV Engineers for a large greenfield biopharmaceutical manufacturing project in Holly Springs ...

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 ...

CQV Engineer Location: Holly Springs, NC We are seeking an experienced CQV Engineer to support a large greenfield biopharmaceutical manufacturing project. The ideal candidate will have strong hands ...

Apply Early

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 ...

CQV Engineer Location: Holly Springs, NC Job Summary Seeking experienced CQV Engineers to support a large greenfield biopharmaceutical manufacturing project. Candidates should have strong hands-on ...

Apply Early

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 ...

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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 ...

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 ...

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 ...

Apply Early

CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...

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Showing results 1-20

Cqv information

See Raleigh, NC salary details

$87.2K

$115K

$140.9K

How much do cqv jobs pay per year?

As of Jul 2, 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 job?

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 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 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 popular job titles related to Cqv jobs in Raleigh, NC? For Cqv jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Cqv jobs in Raleigh, NC look for? The top searched job categories for Cqv jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Cqv jobs? Cities near Raleigh, NC with the most Cqv job openings:
Infographic showing various Cqv job openings in Raleigh, NC as of June 2026, with employment types broken down into 84% Full Time, and 16% Contract. Highlights an 95% In-person, and 5% Hybrid job distribution, with an average salary of $115,026 per year, or $55.3 per hour.
CQV Engineer

CQV Engineer

Intellectt INC

Holly Springs, NC • On-site

Contractor

Posted 12 days ago


Job description

Hello,
I hope you’re doing well.

My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for a CQV Engineer based in Holly Springs, NC with one of our prestigious clients.

I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com

Job Title: CQV Engineer 
Location: Holly Springs, NC
Duration: Long-Term Contract
Summary:

We are hiring experienced CQV Engineers for a large greenfield biopharmaceutical manufacturing project in Holly Springs, NC. Candidates should have strong experience in commissioning, qualification, validation, and startup activities within GMP-regulated pharma or biotech environments.

Key Responsibilities

  • Execute CQV and startup activities for GMP equipment and critical utilities.
  • Develop and execute IQ/OQ protocols, test plans, and turnover documentation.
  • Support startup, troubleshooting, FAT/SAT, walkdowns, and mechanical completion.
  • Review P&IDs, vendor documents, and system assessments.
  • Collaborate with engineering, automation, quality, and operations teams.
  • Ensure compliance with GMP/GDP standards and support CAPA, deviations, and change controls.

Required Skills

  • 5+ years of CQV/startup/validation experience in pharma, biotech, or life sciences.
  • Experience with greenfield projects and upstream/downstream equipment.
  • Hands-on experience with utilities: WFI, Clean Steam, HVAC, Compressed Air, Purified Water, CIP/SIP.
  • Strong GMP documentation and protocol execution experience.
  • Ability to work independently in fast-paced startup environments.

Preferred

  • Experience with DeltaV, Rockwell, Kneat, or ValGenesis.
  • Biologics or sterile manufacturing experience.
  • Bachelor’s degree in Engineering or related field.

Thanks & Regards,
Vyshnavi
Recruiter
Intellectt Inc 
vyshnavi.t@intellectt.com
Direct: 732 204 6550
Desk number: 732 412 6999 - Ext: 225