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Cqv Engineer Jobs (NOW HIRING)

Moderna, Inc.

CQV Engineer II

Norwood, MA · On-site

$74K - $118K/yr

S. in Engineering (Chemical or Mechanical preferred; other related scientific disciplines will be considered). * 2-5 years of CQV or validation experience in cGMP manufacturing environments.

PSC Biotech

CQV Engineer

Los Angeles, CA

$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 ...

PSC Biotech

CQV Engineer

Los Angeles, CA

$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 ...

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 ...

PSC Biotech

CQV Engineer

Los Angeles, CA · On-site

$85K - $100K/yr

Your Role We are hiringexperiencedvalidation engineers responsible for thecommissioning ... Identify and assessrisks associated with CQV activities and develop effectivemitigation strategies.

Moderna Therapeutics

CQV Engineer II

Norwood, MA · Hybrid

$74K - $118K/yr

S. in Engineering (Chemical or Mechanical preferred; other related scientific disciplines will be considered). * 2-5 years of CQV or validation experience in cGMP manufacturing environments.

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How much do cqv engineer jobs pay per year?

As of Jun 19, 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. 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 engineers make $300,000 a year?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $300,000 or more annually, especially with extensive experience, advanced skills, and leadership roles. High-paying engineering positions often require advanced degrees, certifications, and working in high-demand industries or executive-level positions.

What is a CQV Engineer job?

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.

What are the key skills and qualifications needed to thrive in the Cqv Engineer position, and why are they important?

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 engineer makes $500,000 a year?

Highly experienced engineers in specialized fields such as petroleum engineering, aerospace engineering, or certain senior roles in software engineering can earn $500,000 or more annually, often including bonuses and stock options. These positions typically require advanced skills, extensive experience, and often involve leadership or executive responsibilities.
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Cqv Engineer jobs near you
Infographic showing various Cqv Engineer job openings in the United States as of June 2026, with employment types broken down into 100% Contract. Highlights an 87% Physical, 5% Hybrid, and 8% Remote job distribution, with an average salary of $89,183 per year, or $42.9 per hour.

Senior CQV Engineer/Manager

IT Minds LLC

Indianapolis, IN • Hybrid

Other

Posted 3 days ago

Job description

Job Title: Senior CQV Engineer/Manager

Location: Remote / Hybrid / Onsite (Depending on Project Requirements)

Duration: Long-Term Contract

Position Overview

We are seeking an experienced CQV (Commissioning, Qualification & Validation) professional to support and lead validation activities within highly regulated pharmaceutical, biotechnology, and life sciences environments. This role will be responsible for ensuring GMP compliance across facilities, utilities, equipment, manufacturing processes, and computerized systems while driving validation strategies and project execution.

Key Responsibilities

  • Lead and support Commissioning, Qualification, and Validation (CQV) activities for facilities, utilities, equipment, laboratory systems, and manufacturing processes.
  • Develop and execute Validation Master Plans (VMPs), risk assessments, traceability matrices, and validation protocols.
  • Author, review, and approve IQ/OQ/PQ protocols and validation summary reports.
  • Coordinate commissioning and qualification activities for cleanrooms, HVAC systems, water systems (PW/WFI), clean steam, compressed gases, and manufacturing equipment.
  • Support FAT, SAT, startup, and operational readiness activities.
  • Manage deviations, investigations, CAPAs, and change controls.
  • Ensure compliance with FDA, EMA, MHRA, GAMP 5, Annex 11, 21 CFR Part 11, and Data Integrity requirements.
  • Collaborate with Engineering, Manufacturing, Quality Assurance, Automation, Regulatory Affairs, and Validation teams.
  • Support regulatory inspections, audits, and remediation activities.
  • Provide leadership and mentoring to validation engineers and CQV team members.

Required Qualifications

  • Bachelor's degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related field.
  • 10+ years of CQV / Validation experience within pharmaceutical, biotechnology, medical device, or life sciences industries.
  • Strong experience with GMP, cGMP, and regulatory compliance requirements.
  • Extensive hands-on experience with:
    • Commissioning, Qualification & Validation (CQV)
    • IQ / OQ / PQ Execution
    • Validation Master Plans (VMP)
    • Risk Assessments
    • Traceability Matrix Development
    • Deviation, CAPA, and Change Control Management
    • GMP Documentation and Compliance

Technical Experience Required

  • Cleanroom Qualification
  • HVAC Qualification
  • Water Systems (PW/WFI)
  • Clean Steam Systems
  • Compressed Air/Gas Systems
  • Manufacturing Equipment Qualification
  • Packaging Equipment Validation
  • Laboratory Equipment Qualification
  • Process Validation

Computer System Validation (CSV)

Experience validating one or more of the following systems:

  • MES
  • LIMS
  • Empower
  • TrackWise
  • Veeva
  • SAP
  • DeltaV
  • SCADA Systems
  • Laboratory Informatics Systems

Preferred Experience

  • Pharmaceutical or Biotechnology Manufacturing
  • Cell & Gene Therapy
  • Biologics Manufacturing
  • Vaccine Manufacturing
  • Greenfield Facility Startups
  • Large Capital Projects
  • Regulatory Inspection Readiness

Preferred Certifications

  • PMP
  • CQV / Validation Certifications
  • ASQ Certifications (CQE/CQA)
  • ISPE Training
  • Lean Six Sigma Green Belt or Black Belt

Must-Have Skills

  • CQV (Commissioning, Qualification & Validation)
  • GMP / cGMP Compliance
  • IQ/OQ/PQ
  • Validation Master Plans (VMP)
  • Risk Assessments
  • Traceability Matrix
  • CAPA & Deviation Management
  • Cleanroom / HVAC Qualification
  • Utilities Qualification (PW/WFI/Clean Steam)
  • Computer System Validation (CSV)
  • FDA / EMA / GAMP 5 Compliance

Best Regards,

Satya Satish J | Technical Recruiter | IT Minds LLC |

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