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C&Q Engineer Jobs (NOW HIRING)

Bachelors in Engineering + 4 years of Engineering experience. PREFERRED QUALIFICATIONS: 1. C&Q Strategy & Planning * Develop and implement the overall Commissioning & Qualification strategy aligned ...

PR ยท On-site

Collaborate with Quality, Validation, Manufacturing, Engineering, Automation, and cross-functional ... Minimum of 3 years of experience in Commissioning & Qualification (C&Q), Validation, Engineering ...

PR ยท On-site

$40 - $48/hr

Partner with QC, validation, IT, and engineering teams to ensure seamless implementation. General ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...

PR ยท On-site

Collaborate with Quality, Validation, Manufacturing, Engineering, Automation, and cross-functional ... Minimum of 3 years of experience in Commissioning & Qualification (C&Q), Validation, Engineering ...

PR ยท On-site

$40 - $48/hr

Partner with QC, validation, IT, and engineering teams to ensure seamless implementation. General ... Experience Requirements: * 3+ years C&Q experience in the Pharmaceutical Industry. * In-depth ...

PR ยท On-site

Collaborate with Quality, Validation, Manufacturing, Engineering, Automation, and cross-functional ... Minimum of 3 years of experience in Commissioning & Qualification (C&Q), Validation, Engineering ...

Sr Engineer - 35333

Juncos, PR ยท On-site

$101K - $139K/yr

C&Q Strategy & Planning * Develop and implement the overall Commissioning & Qualification strategy ... Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain ...

Ensure C&Q activities are integrated with engineering, construction, automation, validation, quality, and operational readiness plans. * Lead, mentor, and develop multidisciplinary C&Q teams ...

Sr Engineer - 35333

Juncos, PR

$101K - $139K/yr

C&Q Strategy & Planning * Develop and implement the overall Commissioning & Qualification strategy ... Collaborate with Engineering, Validation, Quality Assurance (QA), Manufacturing, and Supply Chain ...

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C Q Engineer information

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$10

$53

$86

How much do c&q engineer jobs pay per hour?

As of Jul 15, 2026, the average hourly pay for c&q engineer in the United States is $53.13, according to ZipRecruiter salary data. Most workers in this role earn between $27.64 and $75.96 per hour, depending on experience, location, and employer.

What are C&Q Engineers?

C&Q Engineers, or Commissioning and Qualification Engineers, are professionals who ensure that systems, equipment, and processes in industries like pharmaceuticals, biotechnology, and manufacturing meet regulatory standards and function as intended. They are responsible for planning, executing, and documenting commissioning (verifying that systems are installed and work correctly) and qualification (demonstrating that systems consistently produce results meeting predetermined criteria). Their work is critical for compliance with regulations such as Good Manufacturing Practice (GMP) and for ensuring product quality and safety.

What is the difference between C&Q Engineer vs Commissioning Technician?

AspectC&Q EngineerCommissioning Technician
CredentialsBachelor's degree in engineering or related field, certifications like PE or CQMTechnical diploma or associate degree, relevant certifications
Work EnvironmentDesign review, project planning, overseeing commissioning processesHands-on testing, equipment startup, field troubleshooting
Industry UsageUsed across industries like oil & gas, power, manufacturingPrimarily in field commissioning, installation projects

The C&Q Engineer typically handles planning, documentation, and oversight of commissioning activities, ensuring compliance and quality. In contrast, the Commissioning Technician focuses on executing testing, startup, and troubleshooting tasks on-site. Both roles are essential in the commissioning process but differ in responsibilities and level of involvement.

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 compensation often involves working in high-demand industries, holding managerial positions, or possessing rare technical expertise and certifications.

What do CQV engineers do?

CQV (Commissioning, Qualification, and Validation) engineers are responsible for ensuring that manufacturing equipment, systems, and processes meet regulatory standards and quality requirements. They develop protocols, perform testing, and document procedures to verify that facilities operate correctly and safely, often working in regulated industries like pharmaceuticals and biotech. Strong knowledge of industry regulations, validation tools, and project management is essential for this role.

What are the key skills and qualifications needed to thrive as a C&Q Engineer, and why are they important?

To thrive as a C&Q (Commissioning and Qualification) Engineer, you need a solid background in engineering or life sciences, with experience in commissioning, qualification, and validation in regulated industries such as pharmaceuticals or biotechnology. Familiarity with industry standards (like GAMP, ASTM E2500), validation protocols, and tools such as PLC/SCADA systems and document management software is crucial. Strong analytical thinking, attention to detail, and excellent communication skills help in problem-solving and collaborating with multidisciplinary teams. These skills ensure that facilities, systems, and equipment meet compliance requirements, supporting safe and reliable manufacturing operations.

How does a C&Q Engineer typically collaborate with cross-functional teams during commissioning and qualification projects?

As a C&Q Engineer, you'll work closely with process engineers, validation teams, project managers, and quality assurance personnel to ensure systems and equipment meet regulatory and client requirements. Collaboration often involves attending multidisciplinary meetings, aligning on project timelines, and sharing critical documentation. Effective communication is key, as you'll coordinate testing activities, resolve technical issues, and provide updates on project progress. This teamwork ensures that commissioning and qualification activities are executed efficiently and in compliance with industry standards.

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 experience can earn higher salaries, often exceeding $150,000. The role often requires knowledge of regulatory standards and validation tools.
More about C Q Engineer jobs
Infographic showing various C&Q Engineer job openings in the United States as of July 2026, with employment types broken down into 95% Full Time, 2% Part Time, and 3% Contract. Highlights an 87% Physical, 4% Hybrid, and 9% Remote job distribution, with an average salary of $110,519 per year, or $53.1 per hour.

CQV Engineer (Commissioning, Qualification & Validation)

PACIV

Indianapolis, IN โ€ข On-site

Full-time

Medical, Retirement, PTO

Posted 14 days ago


Job description

CQV Engineer (Commissioning, Qualification & Validation)
Location: Indianapolis, IN
Travel: Up to 40% Domestic & International Travel
Bring Critical Manufacturing Systems to Life
PACIV stands for Process Automation, Controls, Instrumentation & Validation.
We bring advanced manufacturing to life by delivering world-class automation, validation, and instrumentation solutions. Our teams solve complex challenges, support industry-leading facilities, and make a measurable impact on critical manufacturing operations every day.
We are looking for a CQV Engineer to join our Indianapolis, IN team. In this position, you will support the commissioning, qualification, and validation of manufacturing systems, equipment, facilities, utilities, and automation systems within regulated pharmaceutical environments. You will work on high-impact capital projects that help transform complex systems into operational, compliant, and production-ready assets.
Responsibilities
  • Develop and drive completion of Commissioning & Qualification (C&Q) deliverables, including validation plans, risk assessments, project strategies, user requirements, functional specifications, design specifications, impact assessments, traceability matrices, test cases, engineering studies, and final summary reports.
  • Apply a strong understanding of commissioning and qualification principles to support project execution and regulatory compliance activities.
  • Support pharmaceutical capital projects for:
  • Active pharmaceutical ingredient (API) manufacturing equipment
  • Filling operations
  • Device assembly systems
  • Packaging equipment
  • Facilities and utilities
  • Automation systems
  • Participate in project review meetings, including design reviews, qualification reviews, testing strategy discussions, execution reviews, and project status meetings.
  • Develop, review, and maintain validation and qualification documentation within electronic lifecycle management systems.
  • Assess, document, and support change management activities resulting from design updates, deviations, and testing outcomes.
  • Participate in Factory Acceptance Testing (FAT) and Site Acceptance Testing (SAT) activities.
  • Complete required client training and site-specific onboarding requirements.
  • Perform other duties as assigned.
Qualifications
  • Bachelor's degree in Biomedical or Chemical Engineering.
  • Experience with Commissioning & Qualification (C&Q) deliverables, CQV activities, validation documentation, or relevant academic/project experience.
  • Strong understanding of validation principles and deliverables, including requirements development, design, testing, and reporting.
  • Strong interpersonal, verbal, written, and presentation communication skills.
  • Highly motivated, results-driven mindset with the ability to manage multiple priorities in a fast-paced environment.
  • Demonstrated project management skills and the ability to independently drive assignments to completion.
  • Ability to travel up to 40% domestically and internationally.
Why Join PACIV
  • Work on pharmaceutical manufacturing and life sciences capital projects.
  • Gain hands-on experience with commissioning, qualification, validation, FAT, and SAT activities.
  • Collaborate with experienced engineering, automation, and validation professionals.
  • Build expertise working with manufacturing systems, utilities, facilities, and automation technologies.
  • Contribute to projects that support critical manufacturing operations and production readiness.
Compensation & Benefits
PACIV offers a competitive compensation package designed to support employee well-being and long-term financial success.
  • Generous Paid Time Off: Vacation, Sick Leave, and Company Holidays
  • PACIV pays 90% of yearly health care premiums
  • Health Savings Account (HSA) with Company Contributions
  • 401(k) with Company Match up to 4% and immediate vesting with enrollment

Equal Opportunity Employer
PACIV is an Equal Opportunity Employer and considers all qualified applicants in accordance with applicable federal, state, and local employment laws. Employment is contingent upon successful completion of applicable pre-employment requirements and verification of authorization to work in the United States.
Direct-hire applicants only.
C2C, 1099, and third-party agency submissions will not be considered.
Also Known As
CQV Engineer, Commissioning Engineer, Qualification Engineer, Validation Engineer, C&Q Engineer, Commissioning & Qualification Engineer, Pharmaceutical Validation Engineer, GMP Validation Engineer, Capital Projects Validation Engineer.
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