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Cqv Engineer Jobs in Boston, MA (NOW HIRING)

Fusion Life Sciences

CQV Engineer

Boston, MA · 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.

DPS Group

CQV Engineer

Framingham, MA · On-site

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 ...

Sebela Pharma

CQV/Validation Engineer

Holbrook, MA · 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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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 20, 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.

What are popular job titles related to Cqv Engineer jobs in Boston, MA?

For Cqv Engineer jobs in Boston, MA, the most frequently searched job titles are:

What job categories do people searching Cqv Engineer jobs in Boston, MA look for?

The top searched job categories for Cqv Engineer jobs in Boston, MA are:

Cqv Engineer jobs near you
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.

CQV Engineer

Fusion Life Sciences

Boston, MA • On-site

Contractor

Re-posted 11 days ago

Job description

Job Title : 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. The individual is responsible for executing qualification protocols facilities and collaborate with Global Engineering, Facilities Operations, GIS, QA and PMO throughout the life cycle of the project.
Key Responsibilities:
The responsibilities of this position may include, but are not limited to, the following:

  • Develops and executes qualification and validation test plans and protocols.
  • Ensures that all validation documents align with the current client SOPs, global standards and cGMP guidelines.
  • Coordinates with personnel onsite and other vendors to schedule and execute test plans.
  • If required, coordinates with the construction team and Vertex operations teams to schedule execution of validation activities, safely and effectively.
  • Effectively works with cross functional departmental stakeholders, PMO, GIS, EH&S, Global Security, design teams, EHS and QA.
  • Completes Vertex assigned training and ensures that they are 100% compliant 100% of the time.
  • Supports right-the-first time culture for all documents distributed across the organization.
  • Ensures the Global Engineering reputation and partnership is flourished with the cross-functional teams. 

Minimum qualifications:

  • Receptive to change – Adapts (quickly) to changing circumstances.
  • Minimum Bachelor’s degree in an Engineering (Chemical, Biomedical, Industrial, Biotechnology) or related discipline with 2-4 years of CQV experience or equivalent professional experience.
  • Self-motivated and must be able to work independently with minimal supervision and direction.
  • Experience in developing and executing protocols in GMP industry.
  • Experience using Kaye Validator and Data loggers.
  • Understanding and application of technical principles, theories, and concepts in the field, GMP, ISO, GAMP, ANSI.
  • Ability to learn and demonstrate technical problem solving and troubleshooting skills