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Cqv Engineer Jobs in Boston, MA (NOW HIRING)

Summary DPS is looking for a CQV Engineer to work for a client in New Bedford, MA Key Responsibilities * Become familiar with the user, functional, installation, operation and performance ...

CQV Engineer

Boston, MA ยท On-site

CQV Location : Boston, MA General position summary: The Engineer is actively involved in Commissioning, Qualification, Validation, and Requalification activities for Cell and Gene Therapy facilities.

CQV/Validation Engineer

Holbrook, MA ยท On-site

$33 - $43/hr

The CQV/Validation Engineer is responsible for supporting the activities required to implement the Holbrook site's validation plan in compliance with current industry and regulatory expectations.

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Showing results 1-20

Cqv Engineer information

See Boston, MA salary details

$35.8K

$96.9K

$154.3K

How much do cqv engineer jobs pay per year?

As of Aug 21, 2026, the average yearly pay for cqv engineer in Boston, MA is $96,884.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,200.00 and $118,400.00 per year, depending on experience, location, and employer.

What is a CQV engineer?

A CQV (Commissioning, Qualification, and Validation) Engineer is responsible for ensuring that equipment, systems, and processes within regulated industries, such as pharmaceuticals or biotechnology, meet regulatory and operational requirements. They develop and execute test protocols, troubleshoot issues, and document compliance with industry standards (e.g., FDA, GMP). Their role ensures that manufacturing facilities produce safe and effective products. CQV Engineers often collaborate with cross-functional teams, including quality, engineering, and operations.

What are the key skills and qualifications needed to thrive as a CQV engineer?

To thrive as a CQV (Commissioning, Qualification, and Validation) Engineer, you need a solid background in engineering principles, GMP regulations, and life sciences or pharmaceutical processes, often supported by a relevant degree. Familiarity with quality management systems, risk assessment tools, and software for documentation and validation such as TrackWise or Veeva is commonly required, and certifications like Six Sigma or CQV-specific credentials are valuable. Strong analytical thinking, attention to detail, effective communication, and collaboration skills set top performers apart. These competencies are essential to ensure compliance, project success, and seamless interaction with cross-functional teams in highly regulated environments.

What are some common challenges faced by CQV engineers in the pharmaceutical industry?

CQV Engineers in the pharmaceutical industry often encounter challenges such as managing strict timelines while ensuring full compliance with regulatory standards and adapting to evolving project requirements. They must coordinate with multiple departments including QA, production, and engineering to align project goals and documentation. Additionally, troubleshooting unexpected technical issues and staying updated with the latest industry guidelines can be demanding. However, overcoming these challenges is rewarding, as it directly contributes to the safe and effective delivery of life-saving products.

How much do CQV engineers make in the US?

CQV (Commissioning, Qualification, and Validation) engineers in the US typically earn between $80,000 and $130,000 annually, depending on experience, location, and industry. Senior or specialized engineers with certifications and extensive expertise can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory standards and validation tools.
Infographic showing various Cqv Engineer job openings in Boston, MA as of August 2026, with employment types broken down into 80% Full Time, and 20% Contract. Highlights an 100% In-person job distribution, with an average salary of $96,884 per year, or $46.6 per hour.

Equipment CQV Engineer

Stark Pharma Solutions Inc

Boston, MA โ€ข On-site

Contractor

Posted yesterday

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Job description

Equipment CQV Engineer 

Role: 

Seeking experienced Equipment CQV Engineers to support an onsite GMP equipment qualification program at a biopharmaceutical manufacturing facility. The role focuses on hands-on execution of equipment commissioning and qualification activities across manufacturing, laboratory, and support of equipment in a regulated GMP environment. 

Key Responsibilities: 

  • Review and execute established equipment qualification protocols (IQ/OQ). 

  • Document test results and identify/resolve execution issues. 

  • Support equipment readiness for manufacturing and engineering activities. 

  • Qualify various manufacturing, laboratory, and support equipment. 

  • Partner with Engineering, Validation, Manufacturing, Quality, and equipment vendors. 

  • Work independently, moving quickly through multiple equipment packages. 

Required: 

  • 5–10 years of CQV, equipment validation, or equipment qualification experience. 

  • Strong hands-on experience executing IQ/OQ and other equipment qualification protocols. 

  • Pharmaceutical, biotechnology, biopharmaceutical, cell therapy, or other GMP-regulated manufacturing experience. 

  • Experience qualifying for manufacturing and/or laboratory equipment. 

  • Ability to review protocols, execute testing, document results, and address discrepancies/deviations. 

  • Understanding GMP documentation and good documentation practices.