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Cqv Engineer Jobs in Massachusetts (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.

CAI

Senior Validation Engineer

Boston, MA · On-site

$102K - $111K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Boston, MA

$102K - $111K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

CAI

Senior Validation Engineer

Boston, MA · On-site

$102K - $111K/yr

Key Responsibilities CQV Execution & Safety - Perform Commissioning, Qualification, and Validation ... (BS/BA) in Engineering, Chemistry, or Life Sciences (relevant experience can substitute for ...

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All JobsCqv Engineer JobsCqv Engineer Jobs in Massachusetts

Cqv Engineer information

See Massachusetts salary details

$36K

$97.4K

$155.1K

How much do cqv engineer jobs pay per year?

As of Sep 6, 2026, the average yearly pay for cqv engineer in Massachusetts is $97,399.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,600.00 and $119,000.00 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 Massachusetts?

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

What job categories do people searching Cqv Engineer jobs in Massachusetts look for?

The top searched job categories for Cqv Engineer jobs in Massachusetts are:

What cities in Massachusetts are hiring for Cqv Engineer jobs?

Cities in Massachusetts with the most Cqv Engineer job openings:

Cqv Engineer jobs near you
Infographic showing various Cqv Engineer job openings in Massachusetts as of August 2026, with employment types broken down into 74% Full Time, and 26% Contract. Highlights an 100% In-person job distribution, with an average salary of $97,399 per year, or $46.8 per hour.

CQV Engineer Trainee

Stark Pharma Solutions Inc

Springfield, MA • On-site

Contractor

Re-posted 4 hours ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are currently inviting applications for our CQV Engineer Trainee (FREE Training Program). If you are interested in building a career in the Pharmaceutical, Biotechnology, or Medical Device industry, please send me your updated resume. The program details are as follows.

Job Title: CQV Engineer Trainee (FREE Training Program)
Location: USA
Training Fee: 100% FREE
Experience: Freshers & 0–1 Years (OPT Candidates Welcome)

Position Overview

Stark Pharma Solutions Inc. is offering a FREE industry-focused CQV Engineer Trainee Program for candidates aspiring to build a career in the Pharmaceutical, Biotechnology, and Medical Device industries. This program is designed to provide comprehensive knowledge of Commissioning, Qualification & Validation (CQV), FDA regulations, GMP compliance, and industry best practices to prepare participants for real-world CQV Engineer opportunities.

Key Learning Areas

• Fundamentals of Commissioning, Qualification & Validation (CQV).
• GMP, cGMP, FDA, and regulatory compliance requirements.
• Equipment Qualification – Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ).
• Validation documentation, protocols, reports, and Good Documentation Practices (GDP).
• Qualification of manufacturing equipment, cleanrooms, HVAC systems, utilities, and process equipment.
• Risk Assessment, Change Control, Deviations, and CAPA.
• Validation lifecycle and pharmaceutical industry best practices.
• Resume preparation and interview guidance for CQV Engineer roles.

Program Benefits

• 100% FREE Training – No Registration Fee.
• Industry-focused curriculum delivered by experienced CQV professionals.
• Real-world validation documentation and practical learning.
• Hands-on exposure to CQV concepts and industry standards.
• Resume building and mock interview preparation.
• Career guidance for Pharmaceutical, Biotechnology, and Medical Device industries.
• Opportunity to work on real-time CQV projects after successful completion (based on performance and project availability).
• Potential opportunities for W-2 employment and future visa sponsorship based on performance, business requirements, and eligibility.

Eligibility

• Bachelor's or Master's Degree in Mechanical Engineering, Chemical Engineering, Biotechnology, Biomedical Engineering, Pharmaceutical Sciences, Life Sciences, Biology, Chemistry, or a related discipline.
• Freshers and candidates with 0–1 years of experience.
• OPT/CPT candidates are encouraged to apply.
• Strong communication, analytical, and problem-solving skills.
• Passion to build a career in Commissioning, Qualification & Validation (CQV).

I am actively connecting with aspiring CQV professionals for current and upcoming opportunities. If you are interested in joining this FREE CQV Engineer Training Program, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest training programs and career opportunities:

https://www.linkedin.com/company/99455976/