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Cqv Jobs in Colorado (NOW HIRING)

Join our team with this exciting opportunity to support commissioning Qualification and Validation (CQV) activities (excluding process validation) at our facilities in Colorado. Work in our dynamic ...

Join our team with this exciting opportunity to support commissioning Qualification and Validation (CQV) activities (excluding process validation) at our facilities in Colorado. Work in our dynamic ...

Join our team with this exciting opportunity to support commissioning Qualification and Validation (CQV) activities (excluding process validation) at our facilities in Colorado. Work in our dynamic ...

Showing results 21-30

Cqv information

See Colorado salary details

$93.9K

$113K

$130K

How much do cqv jobs pay per year?

As of Sep 2, 2026, the average yearly pay for cqv in Colorado is $113,037.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,400.00 and $122,400.00 per year, depending on experience, location, and employer.

What is a CQV?

A CQV (Commissioning, Qualification, and Validation) job involves ensuring that equipment, systems, and processes in industries like pharmaceuticals and biotechnology meet regulatory and operational requirements. CQV professionals develop protocols, execute tests, and document compliance to ensure that facilities maintain safety and efficacy standards. They work closely with engineers, quality teams, and regulatory bodies to achieve validated systems.

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

To thrive as a CQV (Commissioning, Qualification, and Validation) specialist, you need a strong background in engineering or life sciences, along with expertise in equipment qualification, validation protocols, and regulatory compliance. Familiarity with industry standards such as cGMP, FDA, and tools like validation software and document management systems is highly valuable. Strong analytical thinking, attention to detail, communication, and teamwork skills are crucial for ensuring project success and regulatory adherence. These skills ensure that pharmaceutical and biotech manufacturing processes meet rigorous quality standards and regulatory requirements.

What are the most common challenges faced by CQV specialists in the pharmaceutical industry?

CQV specialists in the pharmaceutical industry frequently encounter challenges such as managing tight project deadlines, adapting to evolving regulatory requirements, and coordinating across multi-disciplinary teams. Balancing compliance with operational efficiency demands a thorough understanding of documentation and attention to detail. Working with new or complex equipment can also present learning curves that require problem-solving and collaboration with engineering, production, and quality assurance teams. However, overcoming these challenges offers valuable experience and opportunities to build a robust skill set highly regarded in regulated industries.

What does a CQV engineer do?

A CQV (Commissioning, Qualification, and Validation) engineer is responsible for ensuring that manufacturing equipment, systems, and processes meet regulatory standards and quality requirements. They develop and execute validation protocols, perform testing, and document compliance to support product quality and safety in industries like pharmaceuticals and biotech.
Infographic showing various Cqv job openings in Colorado as of August 2026, with employment types broken down into 86% Full Time, 7% Part Time, 6% Contract, and 1% Nights. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $113,037 per year, or $54.3 per hour.

PHARMACEUTICAL - ELECTRICAL ENGINEER

MMR Consulting

Boulder, CO • On-site

Other

Posted 15 days ago


Job description

Previous Pharmaceutical/Biotech experience is preferred for this role.

MMR Consulting is a consulting firm specializing in the pharmaceutical and biotechnology industries. Our services include Project Management, Process, Automation, Facilities and Equipment CQV.

MMR Consulting has offices in Canada, USA, and Australia.

This is an outstanding opportunity to join our growing team, where the successful candidate will work with a group of specialists involved in project management, commissioning, and qualifications of equipment, systems, and facilities.

The work will require working out of the client’s facilities in Raleigh, North Carolina.

RESPONSIBILITIES

  • Work as part of our customer’s in-ouse engineering team, as an electrical systems engineer to support our customer with reviewing document designs/submittals from A/E firms, vendor shop drawings/specs/submittals, construction submittals to ensure owner’s requirements are met.
  • Oversee electrical projects end to end (from start to completion, i.e. design, procurement, construction, commissioning/startup, documentation support/close-out).
  • Provide technical guidance into the design, project management, commissioning and validation, and start-up of various electrical equipment and systems.
  • Review technical data sheets and drawings for various equipment, instrumentation, and systems with a variety of voltages (Low Voltage, and Medium Voltage systems)
  • Perform field job walks, to review the progress / correctness of field activities.
  • Participate in commissioning & startup of electrical systems.
  • Provide technical engineering guidance to junior engineers.
  • Coordination with other engineering disciplines and other cross-functional departments (automation engineering, facilities engineering, process engineering, validation, project management, operations, quality, safety).
  • Coordinate meetings with cross-functional departments, to drive project progress, facilitate decisions, and provide updates.
  • Engage other departments, as required, into design reviews and decisions.
  • Prepare, review, execute commissioning protocols, and reports.
  • Work may require occasional support over shutdowns or extended hours, specifically during installation and commissioning / validation phases.
  • The work will require working out of clients’ facilities.
  • As this position requires working on client sites, you will need to comply with the client’s safety rules.
  • Visit construction and installation sites, wear necessary safety PPE.
  • Supervise contractors during critical installations of process equipment and associated utilities.
  • Other duties assigned by client, and/or MMR, are based on workload and project requirements.

QUALIFICATIONS

  • 6-8+ years of experience in electrical engineering and electrical construction. Will consider candidates with more experience as well for a Senior/SME Role.
  • Knowledge of Low, and Medium Voltage systems (up to 10kV, anything over 10kV is an asset but not required).
  • Experience with the following electrical equipment and systems:
  •  Switchgear
  •  Switchboards
    •  Lighting controls
      •  UPS (uninterruptible power supply) systems
        • Possess leadership skills, and able to take initiative to lead projects, involving multiple stakeholders, departments, and varying complexity.

        Equal Employment Opportunity and Reasonable Accommodations

        MMR Consulting is an equal opportunity employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. Our hiring decisions are based on merit, qualifications, and business needs. We are committed to working with and providing reasonable accommodation to individuals with disabilities globally. If, because of a medical condition or disability, you need reasonable accommodation for any part of the application or interview process, please let us know the nature of your request.