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Cqv Jobs in Raleigh, NC (NOW HIRING)

Visium Resources, Inc.

Pharmaceutical Engineer

Raleigh, NC · On-site

$120K - $145K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Summary We are seeking a highly motivated Senior CQV Engineer to support commissioning, qualification, and validation activities for pharmaceutical and biotechnology manufacturing facilities. The ...

CRB

Walkdown / Turnover Lead

Raleigh, NC · On-site

This role works closely with the Construction, CQV, and Quality teams to support field walkdowns on active construction sites and drive multi-discipline systems through mechanical completion and ...

CAI

Senior Validation Engineer

Raleigh, NC · On-site

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

CRB

Walkdown / Turnover Lead

Raleigh, NC · On-site

This role works closely with the Construction, CQV, and Quality teams to support field walkdowns on active construction sites and drive multi-discipline systems through mechanical completion and ...

CAI

Senior Validation Engineer

Raleigh, NC · On-site

$87K - $120K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation (CQV) activities with a strong focus on safety - Deliver C&Q activities in alignment with project ...

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Showing results 21-40

All JobsCqv JobsCqv Jobs in Raleigh, NC

Cqv information

See Raleigh, NC salary details

$87.2K

$115K

$140.9K

How much do cqv jobs pay per year?

As of Aug 17, 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 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:

Cqv jobs near you
Infographic showing various Cqv job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 73% In-person, and 27% Remote job distribution, with an average salary of $115,026 per year, or $55.3 per hour.

6460 - Senior CQV Engineer / Senior Validation Engineer

Verista, Inc.

Durham, NC • On-site

$101K - $138K/yr

Full-time

Posted 25 days ago

Job description

Senior CQV Engineer Responsibilities:

  • Designing validation plans
  • Conducting and documenting impact and risk assessments with a full understanding of equipment/system/software operation and ability to assess direct, indirect, and no impact systems and functions within complex processes
  • Maintaining (and ensuring the team maintains) clear, detailed records of qualification and validation, and change control activities for future compliance audits
  • Designing and executing engineering studies for critical process parameter definition and verification prior to validation
  • Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader
  • Running test scripts and documenting results
  • Adherence with project schedule for all assigned activities
  • Maintaining clear, detailed records qualification and validation
  • Documenting impact and risk assessments as part of a team
  • Completing user interface testing, software verification, and complete alarm testing on automated systems
  • Developing, reviewing, and executing testing documentation
  • Making recommendations for design or process modification based on test results when executing test scripts
  • General understanding of capital equipment implementation and process knowledge
  • Understanding validation documents, URS, IQ, OQ, PQ

Requirements:

  • Must be able/willing to work onsite in the Raleigh/Durham metropolitan area
  • Must be willing to meet potential future travel requirements (10-50%)
  • Bachelor's Degree or equivalent required
  • Ability to mentor and guide less experienced team members
  • Ability to communicate effectively with clients
  • Proven ability to identify areas of business expansion and report to management team for follow-up
  • Obvious business maturity and interpersonal skills to be able to effectively communicate and collaborate
  • Experience and capability of effectively communicating requirements (written and orally) with rationale to different levels of the client's organization
  • 4 - 6 years of demonstrated role relevant experience
  • Demonstrated experience in leading CQV activities specific to pharmaceutical manufacturing requirements
  • Proficiency using PC and Microsoft Office tools
  • Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
  • Ability to work as part of a team
  • Strong problem-solving and critical thinking skills
  • Excellent organizational and time management skills
  • Strong attention to detail
  • GMP and Good Documentation Practice
  • Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes)
  • Basic skills with EXCEL and PowerPoint
  • Strong interpersonal skills and clear communication capabilities
  • Experience with and tolerance for high levels of challenge and change
  • Experience in GMP regulated environment
  • Proven attention to detail and organization in project work
  • Capable of working on assigned tasks without mentorship

Apply