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Commissioning Qualification Validation Cqv Jobs (NOW HIRING)

FUJIFILM Biotechnologies

Position OverviewThe CQV Engineer 3 supports the commissioning and qualification of equipment and systems for the site. This role performs validation activities to include but not limited to ...

Actalent

Laboratory CQV Specialist

Wilson, NC · On-site

... in commissioning, qualification, and validation (CQV), equipment qualification, or validation ... within a pharmaceutical, biotechnology, or regulated laboratory environment. * Demonstrated ...

Actalent

Laboratory CQV Specialist

Wilson, NC · On-site

... in commissioning, qualification, and validation (CQV), equipment qualification, or validation ... within a pharmaceutical, biotechnology, or regulated laboratory environment. * Demonstrated ...

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Commissioning Qualification Validation Cqv information

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

As of Aug 7, 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 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 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 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 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 91% Full Time, 7% Part Time, and 2% 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.

CQV Engineer

Stark Pharma Solutions Inc

West Valley City, UT • On-site

Contractor

Re-posted 7 days ago

Job description

Hi,

My name is Sravani Dasari from Stark Pharma Solutions Inc. We are hiring talent for our client and are currently working on a CQV Engineer position. Please send me your updated resume if you have relevant experience and are interested in this opportunity. The detailed job description is as follows.

Job Title: CQV Engineer
Location: West Valley City, Utah
Duration: Long Term

Position Overview

We are seeking an experienced CQV Engineer to support Commissioning, Qualification, and Validation (CQV) activities within a pharmaceutical, biotechnology, or medical device manufacturing environment. This role will focus on ensuring that manufacturing equipment, utilities, facilities, and cleanroom systems are commissioned, qualified, and validated in compliance with GMP and regulatory requirements. The ideal candidate will have strong expertise in validation protocols, equipment qualification, regulatory compliance, and cross-functional collaboration to ensure reliable and compliant manufacturing operations.

Key Responsibilities

• Execute Commissioning, Qualification, and Validation (CQV) activities for manufacturing equipment, utilities, facilities, and cleanroom systems.

• Develop, review, and execute Installation Qualification (IQ), Operational Qualification (OQ), and Performance Qualification (PQ) protocols.

• Support commissioning and qualification of process equipment, HVAC systems, clean utilities, and facility infrastructure.

• Ensure compliance with GMP, FDA, ISPE, ASTM, and company quality standards throughout validation activities.

• Prepare validation documentation, technical reports, summary reports, and protocol deviations.

• Collaborate with Engineering, Manufacturing, Quality Assurance, Validation, and Maintenance teams to support project execution.

• Assist with investigations, deviations, CAPA, change control, and risk assessments related to validation activities.

• Participate in equipment startup, factory acceptance testing (FAT), site acceptance testing (SAT), and commissioning activities.

• Maintain validation documentation and ensure all records comply with regulatory and quality system requirements.

• Support continuous improvement initiatives to enhance validation processes, compliance, and operational efficiency.

Required Qualifications

• Bachelor's Degree in Mechanical Engineering, Chemical Engineering, Electrical Engineering, Biomedical Engineering, or a related engineering discipline.

• 3+ years of experience in Commissioning, Qualification, and Validation (CQV), Validation Engineering, or Equipment Qualification within pharmaceutical, biotechnology, or medical device manufacturing environments.

• Hands-on experience developing and executing IQ, OQ, and PQ protocols for manufacturing equipment, utilities, cleanrooms, and facility systems.

• Strong knowledge of GMP, FDA, ISPE, ASTM, validation lifecycle, and regulatory compliance requirements.

• Experience with equipment commissioning, facility qualification, utility validation, and cleanroom validation.

• Familiarity with validation documentation, protocol execution, deviation management, CAPA, change control, and risk assessment processes.

• Experience supporting FAT, SAT, equipment startup, and engineering project activities.

• Strong technical documentation, analytical, troubleshooting, and problem-solving skills.

• Excellent communication and cross-functional collaboration skills with the ability to work effectively in a regulated manufacturing environment.

• Experience working within pharmaceutical, biotechnology, or medical device manufacturing facilities is highly preferred.

• Knowledge of computerized systems validation (CSV), process validation, Lean Manufacturing, or Six Sigma methodologies is an added advantage.

I am actively connecting with professionals for current and upcoming opportunities. If you are open to exploring new roles or would like to stay informed about relevant positions, please send me your updated resume along with the best number and time to reach you.

Please follow Stark Pharma Solutions on LinkedIn for the latest job updates: https://www.linkedin.com/company/99455976/