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Commissioning Qualification Validation Cqv Jobs (NOW HIRING)

Pinnaql

Validation Engineer

Wilson, NC · On-site

Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities. * Develop, review, and ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities. * Develop, review, and ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities. * Develop, review, and ...

Pinnaql

Validation Engineer

Wilson, NC · On-site

Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities. * Develop, review, and ...

Pinnaql

Validation Engineer

Wilson, NC

Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities. * Develop, review, and ...

Pinnaql

Validation Engineer

Wilson, NC

Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities. * Develop, review, and ...

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How much do commissioning qualification validation cqv jobs pay per hour?

As of Sep 1, 2026, the average hourly pay for commissioning qualification validation cqv in the United States is $52.00, according to ZipRecruiter salary data. Most workers in this role earn between $39.42 and $63.22 per hour, depending on experience, location, and employer.

What is a commissioning qualification validation (CQV) professional?

Commissioning, Qualification, and Validation (CQV) professionals are specialists who ensure that equipment, systems, and processes in industries like pharmaceuticals, biotechnology, and manufacturing meet regulatory standards and function as intended. They are responsible for planning, executing, and documenting activities that demonstrate compliance with quality and safety regulations. CQV experts play a critical role in bringing new facilities and systems into operation, guaranteeing that everything is tested and verified according to industry guidelines. Their work helps prevent failures, enhance product quality, and ensure patient or consumer safety.

What are some typical challenges faced by commissioning qualification validation (CQV) professionals during facility start-up projects?

CQV professionals often encounter challenges such as tight project timelines, evolving regulatory requirements, and coordination among cross-functional teams. During facility start-up, balancing documentation accuracy with rapid progress can be demanding, especially when unexpected technical issues arise. Additionally, aligning the expectations of engineering, quality assurance, and operations departments requires strong communication and adaptability. By proactively addressing these challenges, CQV professionals help ensure a smooth transition from construction to validated production.

What are the key skills and qualifications needed to thrive as a commissioning qualification validation (CQV) professional, and why are they important?

To excel as a CQV professional, you need a solid background in engineering or life sciences, comprehensive knowledge of Good Manufacturing Practice (GMP), and experience with commissioning and validation processes. Familiarity with industry-standard software like ValGenesis, TrackWise, and documentation management systems, as well as certifications such as ISPE CQV or Six Sigma, is often required. Attention to detail, strong problem-solving abilities, and effective communication are crucial soft skills in this field. These competencies ensure equipment and processes meet regulatory standards, guarantee product quality, and support successful project delivery in highly regulated industries.

What is the difference between Commissioning Qualification Validation Cqv vs Equipment Validation Specialist?

AspectCommissioning Qualification Validation CqvEquipment Validation Specialist
CredentialsGMP, FDA, or industry-specific certificationsGMP, FDA, or industry-specific certifications
Work EnvironmentPharmaceutical, biotech, or manufacturing facilities during project startupManufacturing or laboratory environments focusing on equipment performance
Employer & Industry UsageUsed in regulated industries for system and process validationUsed for validating individual equipment and systems

While both roles involve validation processes, Cqv focuses on the overall commissioning, qualification, and validation of systems and processes during facility startup. Equipment Validation Specialists primarily validate specific equipment performance. Both require similar certifications and work in regulated manufacturing environments, but their scope differs in focus and responsibilities.

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Commissioning Qualification Validation Cqv jobs near you
Infographic showing various Commissioning Qualification Validation Cqv job openings in the United States as of August 2026, with employment types broken down into 94% Full Time, 5% Part Time, and 1% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $108,152 per year, or $52 per hour.

Validation Engineer

Pinnaql

Wilson, NC • On-site

Full-time

Posted 18 days ago

Job description

Validation & Engineering Group, Inc. (V&EG) a Pinnaql company is a leading services supplier who provides solutions for the Pharmaceutical, Biotechnology, Chemical, Food, and Medical Devices industries in the following areas: Laboratory, Compliance, Computer, Engineering, Project Management, Validation, and other services.
We are seeking a talented, dedicated individual committed to work under the highest ethics standards for the following position:
  • Validation Engineer

Position Overview
We are seeking an experienced Validation Engineer with Commissioning, Qualification & Validation (CQV) experience to support projects within the life sciences industry. The successful candidate will be responsible for executing and documenting commissioning, qualification, and validation activities for facilities, utilities, equipment, systems, and manufacturing processes in accordance with applicable regulatory requirements and Good Manufacturing Practices (GMP).
This role requires strong technical documentation skills, attention to detail, and the ability to work collaboratively with Engineering, Quality, Manufacturing, Automation, and Project Management teams.
Key Responsibilities
  • Execute and support Commissioning, Qualification & Validation (CQV) activities for pharmaceutical, biotechnology, medical device, or other regulated life sciences facilities.
  • Develop, review, and execute validation documentation, including:
    • Validation Plans
    • User Requirements Specifications (URS)
    • Risk Assessments
    • Design/Functional Specifications
    • Commissioning documentation
    • IQ/OQ/PQ protocols and reports
    • Traceability Matrices
    • Summary Reports
  • Support qualification of equipment, facilities, utilities, and manufacturing systems.
  • Perform protocol execution, field verification, data collection, and review of qualification results.
  • Ensure validation activities are performed in compliance with GMP, FDA, EU GMP, and applicable industry standards.
  • Participate in FMEA/risk assessments and apply a risk-based approach to validation activities.
  • Support deviations, investigations, CAPA, and change control activities associated with validation projects.
  • Review engineering and technical documentation to ensure validation requirements are adequately addressed.
  • Collaborate with Engineering, Quality Assurance, Manufacturing, Automation, Facilities, and other project stakeholders.
  • Track validation deliverables, schedules, open items, and project milestones.
  • Support commissioning activities and transition from commissioning into formal qualification.
  • Ensure validation documentation is complete, accurate, and audit-ready.
  • Participate in client meetings, project status meetings, and technical reviews.
  • Provide technical support during regulatory or client inspections, as required.

CQV Experience
Candidates should have hands-on experience with some combination of:
  • Commissioning and qualification of process equipment
  • Facility and utility qualification
  • Cleanrooms and controlled environments
  • HVAC systems
  • Purified Water / WFI systems
  • Compressed gases and process gases
  • Autoclaves, sterilizers, and/or depyrogenation equipment
  • Manufacturing and laboratory equipment
  • Temperature-controlled systems
  • Process systems and supporting utilities
  • Equipment and system turnover documentation
  • IQ/OQ/PQ execution

Required Qualifications
  • Bachelor's degree in Engineering, Science, or a related technical discipline.
  • 3+ years of validation, qualification, commissioning, or CQV experience within a regulated life sciences environment.
  • Experience working in pharmaceutical, biotechnology, medical device, or other GMP-regulated industries.
  • Strong understanding of GMP and validation principles.
  • Experience developing and/or executing validation and qualification protocols.
  • Experience with risk-based validation methodologies.
  • Strong technical writing and documentation skills.
  • Ability to interpret engineering drawings, specifications, procedures, and technical documentation.
  • Strong organizational and project management skills.
  • Ability to work independently and collaboratively in a project environment.

At Validation & Engineering Group, people always come first. We believe that when you're empowered to do your best work, bold ideas thrive and real progress happens. This isn't just a job - it's an opportunity to make a meaningful difference by shaping the future of healthcare and technology alongside a purpose-driven, supportive team.
Excited to build something meaningful together? We look forward to hearing from you.
Validation & Engineering Group is an equal opportunity employer. All applicants will be considered for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran status, or disability status.

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