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Cqv Engineer Jobs (NOW HIRING)

Lonza

CQV Engineer

Bend, OR

CQV Engineer Bend, OR The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed. Today, Lonza is a global ...

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 ...

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.

Fujifilm

CQV Engineer 2

Holly Springs, NC · On-site

Position Overview The CQV Engineer 2 supports the commissioning and qualification of equipment and systems for the site. This role coordinates with the CQV team to perform validation activities to ...

Fujifilm

CQV Engineer 2

Holly Springs, NC

The CQV Engineer 2 supports the commissioning and qualification of equipment and systems for the site. This role coordinates with the CQV team to perform validation activities to include but not ...

PM Group

CQV Engineer III

Oceanside, CA

$100K - $130K/yr

Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team near Oceanside, CA . Outsourced Technical Services (OTS ...

New

FUJIFILM Biotechnologies

Position OverviewThe CQV Engineer 2 supports the commissioning and qualification of equipment and systems for the site. This role coordinates with the CQV team to perform validation activities to ...

Fujifilm

CQV Engineer 2

Holly Springs, NC · On-site

Position Overview The CQV Engineer 2 supports the commissioning and qualification of equipment and systems for the site. This role coordinates with the CQV team to perform validation activities to ...

PM Group

CQV Engineer III

San Diego, CA · On-site

$100K - $130K/yr

Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Outsourced Technical Services(OTS) team near San Diego, CA . Outsourced Technical Services (OTS ...

PSC Biotech

CQV Engineer

Los Angeles, CA · On-site

$85K - $100K/yr

Our engineers play a critical role in driving project success, while supporting validation planning ... Identify and assess risks associated with CQV activities and develop effective mitigation ...

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CQV Engineer information

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$33K

$89.2K

$142K

How much do cqv engineer jobs pay per year?

As of Aug 7, 2026, the average yearly pay for cqv engineer in the United States is $89,183.00, according to ZipRecruiter salary data. Most workers in this role earn between $66,500.00 and $109,000.00 per year, depending on experience, location, and employer.

What does a CQV engineer do?

A CQV (Commissioning, Qualification, and Validation) engineer is responsible for ensuring that manufacturing equipment, systems, and processes in industries like pharmaceuticals and biotech meet regulatory standards and quality requirements. They develop protocols, perform testing, and document procedures to verify that systems operate correctly and consistently. CQV engineers often work with validation tools, follow strict compliance guidelines, and collaborate with cross-functional teams during project execution.

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 sector. 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 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 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?

CQV (Commissioning, Qualification, and Validation) engineers in Ireland typically earn between €40,000 and €70,000 annually, depending on experience, qualifications, and the industry sector. Senior or specialized engineers with certifications such as PMP or ISA may earn higher salaries, especially in pharmaceutical or biotech manufacturing environments.

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.

More about CQV Engineer jobs
What cities are hiring for Cqv Engineer jobs? Cities with the most Cqv Engineer job openings:
What states have the most Cqv Engineer jobs? States with the most job openings for Cqv Engineer jobs include:
What job categories do people searching Cqv Engineer jobs look for? The top searched job categories for Cqv Engineer jobs are:
CQV Engineer jobs near you
Infographic showing various Cqv Engineer job openings in the United States as of August 2026, with employment types broken down into 92% Full Time, 2% Part Time, and 6% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $89,183 per year, or $42.9 per hour.

CQV Engineer

Lonza

Bend, OR

Full-time

Medical, Dental, Vision

Re-posted 27 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

24th of 86 rated pharmaceutical

Job description

CQV Engineer

Bend, OR

The actual location of this job is in Bend, Oregon (USA). Relocation assistance is available for eligible candidates and their families, if needed.

Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there's no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that's the kind of work we want to be part of.

What you will get:

  • An agile career and dynamic working culture.

  • An inclusive and ethical workplace.

  • Compensation programs that recognize high performance.

  • Medical, dental, and vision insurance.

  • Access to Lonza's global benefits program.

What you will do:

  • Partner with engineering, QA, and manufacturing teams to support smooth project execution.

  • Troubleshoot and improve equipment, processes, and systems.

  • Write, review, and execute qualification protocols (IQ/OQ/PQ) for new and existing equipment.

  • Identify risks to product quality and apply mitigation strategies.

  • Generate validation reports and maintain compliant documentation following FDA and cGMP guidelines.

  • Manage and close deviations or nonconformances identified during testing.

  • Support engineering documentation such as user requirements and design qualification materials.

What we are looking for:

  • High School Diploma or GED required; engineering degree preferred.

  • 3-5 years of experience

  • Experience in CQV and temperature mapping.

  • Experience in Operational and Performance qualification testing

  • Understanding of FDA, ICH, ISPE, and ISO guidelines.

  • Proficiency with Microsoft Word and Excel.

  • Ability to solve problems and work crossfunctionally.

  • Strong communication and documentation skills.

  • Interest in improving systems and supporting safe, effective drug development.

About Lonza

At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we offer equal employment opportunities to all qualified applicants regardless of race, religion, color, national origin, sex, sexual orientation, gender identity, age, disability, veteran status, or any other characteristic protected by law. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

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