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Cqv Engineer Jobs in Ohio (NOW HIRING)

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

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

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

We are seeking a mid-level Automation Engineer to play a pivotal role in designing, implementing ... Lead commissioning and qualification (CQV) processes. Ensure technologies and processes are ...

OH · On-site

$100K - $131K/yr

Job Title: Sr. Cold Room Automation Engineer Location: Ohio (Hybrid - 50% Onsite) Duration: 12 ... Strong CQV, Validation, Commissioning, and Startup experience * Knowledge of PLC, HMI, SCADA, OT ...

Senior Automation Engineer

Lewis Center, OH

$98K - $129K/yr

Support Commissioning, Qualification, and Validation (CQV) activities for the cold room systems ... Serve as a recognized Engineering Subject Matter Expert (SME) for cold room systems, establishing ...

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Showing results 1-20

Cqv Engineer information

See Ohio salary details

$31.4K

$84.8K

$135K

How much do cqv engineer jobs pay per year?

As of Aug 14, 2026, the average yearly pay for cqv engineer in Ohio is $84,786.00, according to ZipRecruiter salary data. Most workers in this role earn between $63,200.00 and $103,600.00 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.

Infographic showing various Cqv Engineer job openings in Ohio as of August 2026, with employment types broken down into 90% Full Time, 2% Part Time, and 8% Contract. Highlights an 86% Physical, 5% Hybrid, and 9% Remote job distribution, with an average salary of $84,786 per year, or $40.8 per hour.

6348 - Validation Engineer / CQV Engineer

Verista, Inc.

Columbus, OH

Full-time

Posted 7 days ago


Job description

Validation/CQV Engineer Responsibilities:

  • Authoring, editing, and executing technical commissioning, qualification and validation documentation for standard equipment/systems/ software, and processes as part of team as directed by the project leader
  • Running test scripts and documenting results
  • Adherence with project schedule for all assigned activities
  • Maintaining clear, detailed records qualification and validation
  • Reading technical schematics to identify, locate, and test photo sensors, verify part numbers, and complete I/O testing on automated manufacturing equipment

Requirements:

  • Bachelor's Degree or equivalent required
  • Prior experience supporting validation, qualification, or testing activities for packaging equipment or packaging lines preferred
  • Experience working in or supporting pharmaceutical, medical device, combination product, or regulated packaging operations is a plus
  • Proficiency using PC and Microsoft Office tools
  • Outgoing personality with strong ability to communicate effectively with peers in clear, concise terms
  • Ability to work as part of a team
  • Strong problem-solving and critical thinking skills
  • Excellent organizational and time management skills
  • Strong attention to detail
  • GMP and Good Documentation Practice training (may be completed at onboarding)
  • Intermediate skills with WORD (authoring/editing large technical documents with styles, tables, TOCs, track changes)
  • Basic skills with EXCEL and PowerPoint
  • Strong interpersonal skills and clear communication capabilities