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Cqv Engineer Jobs (NOW HIRING)

Lonza

CQV Engineer

Bend, OR

High School Diploma or GED required; engineering degree preferred. * Experience in CQV and temperature mapping. * Understanding of FDA, ICH, ISPE, and ISO guidelines. * Proficiency with Microsoft ...

Veg Group

$90 - $130/hr

Summary We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in multiple bottle and cap ...

New

Veg Group

Senior Packaging CQV Engineer

Greenville, SC · On-site

$90 - $130/hr

Summary We are seeking a Senior CQV / Packaging Validation Engineer to lead qualification and validation activities for a new packaging line handling liquid products in multiple bottle and cap ...

New

Verista, Inc.

CQV Engineer (New Grad)

Portland, ME · On-site

We constantly acquire new skills and learn from our experiences to enhance our collective expertise CQV Engineer Responsibilities: * New or recent graduates are encouraged to apply * Authoring ...

Eliquent Life Sciences, Inc

CQV Engineer

Indianapolis, IN · On-site

$80K - $95K/yr

The Validation Engineer is an FTE project based role. The Validation Engineer is responsible for the theory and content of validation documents for new cleanrooms and packaging equipment, including ...

Verista, Inc.

CQV Engineer (New Grad)

Columbus, OH · On-site

We constantly acquire new skills and learn from our experiences to enhance our collective expertise CQV Engineer Responsibilities: * Authoring, editing, and executing technical commissioning ...

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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 22, 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 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.
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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 67% Full Time, and 33% Contract. Highlights an 100% In-person 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 12 days ago

Lonza rating

8.3

Company rating: 8.3 out of 10

Based on 42 frontline employees who took The Breakroom Quiz

25th of 86 rated pharmaceutical

Job description

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.
  • Experience in CQV and temperature mapping.
  • 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.

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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