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Cqv Jobs in Raleigh, NC (NOW HIRING)

Eupry

Validation Team Manager (Raleigh, NC)

Raleigh, NC · On-site

Join us at Eupry and take the helm of a talented group of validation engineers who are delivering industry-leading CQV (Commissioning, Qualification, and Validation) services to global pharmaceutical ...

Eupry

Validation Team Manager (Raleigh, NC)

Raleigh, NC · On-site

Join us at Eupry and take the helm of a talented group of validation engineers who are delivering industry-leading CQV (Commissioning, Qualification, and Validation) services to global pharmaceutical ...

MedPharm

Cleaning Validation Engineer

Durham, NC · On-site

Lead CQV activities for CIP, COP, parts washers, and manual cleaning systems Cleaning Optimization & Troubleshooting * Optimize cleaning cycles using key parameters (flow, temperature, detergent ...

MedPharm

Cleaning Validation Engineer

Durham, NC · On-site

Lead CQV activities for CIP, COP, parts washers, and manual cleaning systems Cleaning Optimization & Troubleshooting * Optimize cleaning cycles using key parameters (flow, temperature, detergent ...

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Showing results 41-60

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.

Validation Project Lead / Documentation Audit Lead

FST Technical Services

Durham, NC • On-site

Full-time

Posted 18 days ago

Job description

Validation Project Lead / Documentation Audit Lead
Major Pharmaceutical Facility Construction Project
Location: Durham, NC - FST Life Science office
FST Technical Services is seeking an experienced Validation Project Lead / Documentation Audit Lead to support a large pharmaceutical manufacturing facility construction project.
This role is responsible for establishing a standardized process for the validation of hygienic welding documentation (Isometrics) to ensure compliance with project specifications, applicable codes (e.g., ASME BPE), and industry best practices to support full traceability for hygienic systems..
Responsibilities
  • Lead documentation audit activities to ensure full traceability of hygienic piping systems.
  • Manage schedule, priorities, milestones, and deliverables.
  • Audit weld documentation packages for GMP and Good Documentation Practices (GDP) compliance.
  • Ensure document traceability.
  • Coordinate resolution of documentation deficiencies and quality observations.
  • Partner with Construction Management, Fabricators and Client representatives.
  • Maintain validation metrics and documentation status reports.
  • Mentor junior validation specialists and documentation specialists.
Required Qualifications
  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related technical discipline (or equivalent experience).
  • 8+ years of pharmaceutical validation, CQV, QA, or GMP documentation experience.
  • 3+ years leading validation documentation or CQV teams on large pharmaceutical capital projects.
  • Strong knowledge of FDA cGMP regulations (21 CFR Parts 210 & 211).
  • Thorough understanding of Good Documentation Practices (GDP).
  • Experience supporting Commissioning, Qualification & Validation activities.
  • Experience preparing projects for client and regulatory audits.
  • Excellent project management, organization, and communication skills.
Preferred Qualifications
  • Experience with Traceability Matrices, ALCOA+, Equipment & Utilities Installation Qualification,
Experience with EIDA, Bluebeam, Microsoft Office and SharePoint.

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