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Cqv Engineer Jobs (NOW HIRING)

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · On-site

CQV Engineer Location: Austin, TX Duration: Long Term Position Overview We are seeking an experienced CQV Engineer to support Commissioning, Qualification, and Validation (CQV) activities for ...

CAI

CQV Engineer

Milano, TX

The CQV Engineer develops the documentation to support Commissioning, Qualifications, and Validation. These people are responsible for protocol writing and execution, field verification, and ...

CRB

CQV Engineer III

Raleigh, NC · On-site

The CQV Engineer II will develop and implement commissioning strategies, lead verification activities, and manage deliverables in alignment with project timelines and quality standards. The position ...

CRB

CQV Engineer III

Raleigh, NC · On-site

The CQV Engineer II will develop and implement commissioning strategies, lead verification activities, and manage deliverables in alignment with project timelines and quality standards. The position ...

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.

Lonza

CQV Engineer

Bend, OR · On-site

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 ...

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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

Stark Pharma Solutions Inc

Philadelphia, PA • On-site

Contractor

Re-posted yesterday

Job description

Job Title: CQV Engineer
Location: Philadelphia, PA
Duration: Long Term Contract

Job Summary

We are seeking a highly motivated CQV (Commissioning, Qualification, and Validation) Engineer to support commissioning and qualification activities within a GMP-regulated biopharmaceutical manufacturing environment. The CQV Engineer will be responsible for supporting equipment startup, system qualification, utility validation, and process readiness activities to ensure compliance with FDA, cGMP, and industry standards.

The ideal candidate will work closely with Engineering, Manufacturing, Quality Assurance, Validation, and Automation teams to support capital projects, facility expansion initiatives, and manufacturing operations.

Key Responsibilities

  • Support commissioning and qualification activities for manufacturing equipment, process systems, utilities, and cleanroom environments
  • Develop and execute commissioning and qualification documentation including FAT, SAT, IQ, OQ, and PQ protocols
  • Perform equipment qualification for biopharmaceutical manufacturing systems including upstream and downstream process equipment
  • Support utility qualification activities involving HVAC, purified water systems, clean steam, compressed gases, and environmental monitoring systems
  • Coordinate system walkdowns, punch list management, and turnover documentation activities
  • Ensure all CQV activities comply with FDA, cGMP, GDP, and company quality standards
  • Collaborate with Automation, Engineering, Validation, and Quality teams during equipment installation, startup, and qualification phases
  • Assist with deviation investigations, change control activities, and CAPA implementation related to CQV processes
  • Review P&IDs, engineering drawings, SOPs, and technical documentation to support qualification activities
  • Support technology transfer and facility expansion projects within GMP manufacturing environments
  • Participate in internal audits and regulatory inspections by providing CQV documentation and technical support

Required Qualifications

  • Bachelor’s degree in Chemical Engineering, Mechanical Engineering, Biomedical Engineering, Biotechnology, or related technical field
  • 3+ years of CQV, validation, or qualification experience within biopharmaceutical, pharmaceutical, or regulated manufacturing industries
  • Strong understanding of cGMP, FDA regulations, GDP, and validation lifecycle practices
  • Experience executing IQ/OQ/PQ protocols and commissioning activities
  • Knowledge of clean utilities, HVAC systems, aseptic processing, and GMP facility operations
  • Familiarity with deviation management, CAPA, and change control systems
  • Ability to read and interpret P&IDs, engineering drawings, and technical specifications
  • Strong communication, technical writing, and problem-solving skills