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Cqv Engineer Jobs in California (NOW HIRING)

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 ...

PM Group

CQV Engineer III

Oceanside, 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 Oceanside, CA . Outsourced Technical Services (OTS ...

Inc. (Vti)

Sr CQV Engineer (TCU & HVAC)

Oceanside, CA · On-site

$130 - $170/hr

Sr. Commissioning, Qualification and Validation (CQV) Engineer Location: Oceanside, California -- On-site 40 Hours a week Assignment Duration: September 2026 through March 2027 Extension Potential:

Moderna Therapeutics

$130K - $209K/yr

... and Validation (CQV) scope, and manage contractor priorities. * Drive results by owning and ... Engineer, CQV Engineer or related position in a cGMP manufacturing environment. * 5 years of ...

PSC Biotech

CQV Project Manager

Oceanside, CA · On-site

$115K - $140K/yr

Requirements Bachelor's degree in related engineering discipline. 5+ years of experience managing end-to-end CQV activities for capital projects, including URS development, FAT/SAT execution, and ...

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Cqv Engineer information

See California salary details

$32.6K

$88K

$140.1K

How much do cqv engineer jobs pay per year?

As of Aug 23, 2026, the average yearly pay for cqv engineer in California is $88,015.00, according to ZipRecruiter salary data. Most workers in this role earn between $65,600.00 and $107,600.00 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 California?

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

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

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

What cities in California are hiring for Cqv Engineer jobs?

Cities in California with the most Cqv Engineer job openings:

Cqv Engineer jobs near you
Infographic showing various Cqv Engineer job openings in California 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 $88,015 per year, or $42.3 per hour.

Lead CQV Engineer - Pharmaceutical Manufacturing - Major CAPEX Projects

The International Society for Pharmaceutical Engineering, Inc.

Sonoma, CA • On-site

$140 - $190/hr

Other

Posted 2 days ago

New

Job description

Lead CQV Engineer - Pharmaceutical Manufacturing - Major CAPEX Projects

A global pharmaceutical manufacturer is looking for an experienced Lead CQV Engineer to play a key role in the delivery of major capital investment projects across a flagship GMP manufacturing site.

Working as part of a high-performing engineering team, you'll lead all CQV activities, ensuring new facilities, utilities, equipment and processes are successfully brought into GMP-compliant operation.

What you'll be doing
  • Lead the full CQV lifecycle across major pharmaceutical CAPEX projects.
  • Develop and execute Commissioning & Qualification strategies, plans and protocols.
  • Manage FAT, SAT, IQ, OQ and support PQ activities for manufacturing equipment, clean utilities and facilities.
  • Coordinate with Engineering, Quality, Validation, Operations and project teams to ensure successful project delivery.
  • Ensure all commissioning and qualification activities comply with GMP, FDA and global regulatory requirements.
  • Support project schedules, technical issue resolution, risk management and operational handover.
Experience
  • Proven experience leading CQV activities within pharmaceutical, biotech or other GMP-regulated manufacturing environments.
  • Strong knowledge of GMP, validation, cleanrooms, process equipment and utilities.
  • Experience delivering CQV on large CAPEX or facility expansion projects.
  • Excellent stakeholder management and leadership skills with the ability to coordinate multidisciplinary teams.
  • A structured, quality-focused approach with a strong understanding of regulatory compliance.

This is an excellent opportunity to join a global pharmaceutical organisation at the forefront of major manufacturing investment, where you'll play a key role in delivering cutting-edge GMP facilities and shaping the successful completion of high-value CAPEX programmes.

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