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Cqv Jobs (NOW HIRING)

$79K - $104K/yr

CQV Lead Utilities Location: Netherlands Contract Type: Staff or Contract (12-month project) Job Summary We are seeking a CQV Lead - Utilities (Team Lead) to lead a team of engineers and specialists ...

CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...

CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / PreSales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight to ...

CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...

CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...

Arcadis is seeking a CQV PM to manage the entire program for our client in Wisconsin. Role accountabilities: • Refine Program Level Strategy for assigned workstream • Develop detailed activity ...

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

CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / Pre‑Sales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight ...

We are seeking a CQV Subject Matter Expert with a dual mandate: (1) Business Development / Pre-Sales to shape opportunities, lead solutioning, and win new CQV programs; and (2) Delivery Oversight to ...

Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a proven track record of successfully delivering ...

Turner & Townsend is seeking an experienced Senior CQV Scheduler to join our team to support scheduling as a project controls function on a large-scale project. The ideal individual will have a ...

CQV Consultant - Upstream / Downstream / CIP / PSE / Clean Utilities Location: Holly Springs (100% Onsite) Type: Long-Term Contract Start Date: ASAP Overview We are seeking experienced CQV ...

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Cqv information

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$91K

$120K

$147K

How much do cqv jobs pay per year?

As of Jul 23, 2026, the average yearly pay for cqv in the United States is $120,000.00, according to ZipRecruiter salary data. Most workers in this role earn between $108,000.00 and $131,500.00 per year, depending on experience, location, and employer.

What is a CQV job?

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 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 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.

More about Cqv jobs
What cities are hiring for Cqv jobs? Cities with the most Cqv job openings:
What are the most commonly searched types of Cqv jobs? The most popular types of Cqv jobs are:
What states have the most Cqv jobs? States with the most job openings for Cqv jobs include:
Infographic showing various Cqv job openings in the United States as of July 2026, with employment types broken down into 93% Full Time, 1% Part Time, and 6% Contract. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $120,000 per year, or $57.7 per hour.
CQV Lead Utilities

$79K - $104K/yr

Full-time

Posted 3 days ago


Job description

CAI Overview
Are You Ready?
CAI is a professional services company established in 1996 that has grown year over year to nearly 800 people worldwide. For Life Sciences and Mission Critical industries that need to deliver critical solutions in high-stakes environments, we provide accelerated operational readiness and unparalleled performance at the highest standard through our rigorous approach, field-tested processes, and elite expertise developed over 30 years.
 
Our approach is simple because our Purpose informs everything we do:
We exist to be the trusted solution for our clients as they strive to build a better working world and improve the human experience.
At CAI, we are committed to living our Foundational Principles, both professionally and personally:
We act with integrity
We serve each other
We serve society
We work for our future
 
At CAI, we believe in a relentless dedication to excellence, pushing boundaries and surpassing expectations. From the beginning, we've challenged ourselves to do what others wouldn't. Not just setting industry standards, but redefining them entirely. We are bold in our thinking and creative in our approach. We operate at the intersection of wisdom and technology and thrive when they come together with humanity. For us, operational readiness isn't simply a goal. It's a way of life. Because tomorrow demands to be at the forefront of today. We do this through tireless effort, precision, efficiency and an unwavering belief that there is always room for advancement. We're not interested in how it used to be done. We're obsessed with how it will be done.
 
Job Title: CQV Lead Utilities
Location: Netherlands
Contract Type: Staff or Contract (12-month project)
 
Job Summary
We are seeking a CQV Lead - Utilities (Team Lead) to lead a team of engineers and specialists in the Commissioning, Qualification, and Validation (CQV) of critical utility systems within a GMP pharmaceutical environment. This role will be responsible for planning, coordinating, and overseeing CQV activities across clean and black utilities, ensuring successful delivery on time, on budget, and fully compliant with regulatory standards.
 
Key Responsibilities
Lead and manage a team of CQV engineers, contractors, and specialists in all commissioning and qualification activities.
Oversee CQV activities for clean and black utility systems (Purified Water (PW), WFI (Water for Injection), Clean Steam, Process Gases, HVAC systems, Cooling Towers).
Act as the CQV Subject Matter Expert (SME) for utilities throughout the project lifecycle.
Develop, execute, and approve commissioning and qualification documentation, including IQ/OQ (PQ where applicable).
Lead and support commissioning activities, ensuring systems are installed, tested, and operate as designed.
Review and approve URS, design specifications, risk assessments, and CQV deliverables.
Ensure compliance with EU GMP, FDA, ISPE Baseline Guides, and internal quality standards.
Coordinate CQV activities with Engineering, Quality, Automation, and Operations teams.
Monitor progress, resource allocation, and quality of CQV deliverables, ensuring timelines are met.
Support deviations, change controls, and impact assessments related to utilities.
Represent the utilities team during regulatory inspections and audits.
 
Key Requirements
Experience in pharmaceutical or biopharmaceutical environments with team leadership responsibility.
Strong hands-on experience in Commissioning of utility systems (key requirement).
Proven CQV experience with clean and black utilities, including PW, WFI, clean steam, HVAC, process gases, and cooling towers.
Experience using Kneat (e-validation system) - training will be provided if required.
Knowledge of GMP, ISPE Baseline Guides, and regulatory compliance requirements.
Excellent leadership, communication, and stakeholder management skills.
Ability to prioritize and manage multiple activities in a fast-paced project environment.
 
Other Requirements
Must be able to commit to a minimum 40-hour work week, with flexibility based on project needs.
This role is site based.
Eligible to work in the EU without the need for visa sponsorship, now or in the future.
 
 
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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