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Cqv Engineer Jobs (NOW HIRING)

Stark Pharma Solutions Inc

CQV Engineer

Charlotte, NC · On-site

CQV Engineer Location: North Carolina Duration: Long Term Job Overview We are seeking a CQV Engineer with strong experience in pharmaceutical manufacturing and regulated environments to support ...

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 ...

Pioneer GMP Consulting

CQV Engineer

Louisville, CO · On-site

CQV Engineer - Periodic Review and Requalification * Location: Louisville, CO * Work Type: 100% Onsite * Anticipated Start: Q1 2027 * Initial Duration: Approximately 3-6 Months * Schedule ...

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 ...

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 ...

CAI

CAI is seeking experienced Commissioning, Qualification & Validation (CQV) Engineers to support a large scale pharmaceutical manufacturing project in the Netherlands. This role offers the opportunity ...

CAI

CAI is seeking experienced Commissioning, Qualification & Validation (CQV) Engineers to support a large scale pharmaceutical manufacturing project. This role offers the opportunity to work within a ...

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.

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 ...

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

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$142K

How much do cqv engineer jobs pay per year?

As of Sep 12, 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

Charlotte, NC • On-site

Stark Pharma Solutions Inc
See more jobs at Stark Pharma Solutions Incexternal

Contractor

Posted 8 days ago

Job description

About the Company

Stark Pharma Solutions Inc. is a global consulting and staffing partner established in 2014, serving the Pharmaceutical, Medical Device, Biotech, and IT industries across the USA, Canada, and India. We provide specialized consulting and staffing solutions across Quality & Validation, Regulatory Affairs, R&D, Manufacturing, Supply Chain, Project Management, and IT, with a focus on delivering tailored solutions that drive growth, operational excellence, and long-term client success.

Position: CQV Engineer

Location: North Carolina

Duration: Long Term

Job Overview

We are seeking a CQV Engineer with strong experience in pharmaceutical manufacturing and regulated environments to support commissioning, qualification, and validation activities for facilities, utilities, equipment, and systems.

Key Responsibilities

• Develop, execute, and document commissioning and qualification protocols.
• Perform IQ, OQ, and PQ activities for equipment, utilities, and systems.
• Support commissioning and qualification of pharmaceutical manufacturing facilities and equipment.
• Prepare and maintain CQV protocols, reports, and validation documentation.
• Support FAT, SAT, commissioning, and qualification activities.
• Work with Engineering, Quality, Manufacturing, and Project teams to resolve CQV issues.
• Support deviations, investigations, change controls, and CAPA activities.
• Ensure CQV activities comply with GMP, FDA, and GxP requirements.
• Support continuous improvement and project execution activities.

Required Qualifications

• Bachelor’s degree in Engineering, Life Sciences, or a related technical field.
• 3+ years of experience in CQV, Commissioning, Qualification, or Validation within the pharmaceutical or biotech industry.
• Hands-on experience with IQ/OQ/PQ activities.
• Experience with pharmaceutical facilities, utilities, equipment, or systems.
• Knowledge of GMP, FDA, GxP, and validation requirements.
• Experience preparing and executing CQV protocols and reports.
• Strong documentation, analytical, communication, and problem-solving skills.
• Ability to work effectively with cross-functional teams.

How to Apply

Apply Now: Submit your updated resume to Stark Pharma Solutions Inc. for consideration.
Stark Pharma is an Equal Opportunity Employer and welcomes qualified candidates from diverse
backgrounds.