Philadelphia, PA · On-site
CQV Engineer Location: Philadelphia, PA Duration: Long Term Contract Job Summary We are seeking a highly motivated CQV (Commissioning, Qualification, and Validation) Engineer to support commissioning ...
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Philadelphia, PA · On-site
CQV Engineer Location: Philadelphia, PA Duration: Long Term Contract Job Summary We are seeking a highly motivated CQV (Commissioning, Qualification, and Validation) Engineer to support commissioning ...
Harvard, MA · On-site
Hi, Hope you are doing well, We are looking for " CQV Engineer " Please let me know if you are looking for this role and send me your updated resume also. Job Title - CQV Engineer Job Location
Harvard, MA · On-site
Hi, Hope you are doing well, We are looking for " CQV Engineer " Please let me know if you are looking for this role and send me your updated resume also. Job Title - CQV Engineer Job Location
Framingham, MA · On-site
CQV Specialist Location: Framingham, MA (Onsite) Duration: 6+ months Job Summary: The CQV Specialist will support commissioning, qualification, and validation activities for utilities, equipment, and ...
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Framingham, MA · On-site
CQV Specialist Location: Framingham, MA (Onsite) Duration: 6+ months Job Summary: The CQV Specialist will support commissioning, qualification, and validation activities for utilities, equipment, and ...
South Plainfield, NJ · On-site
CQV Engineer Summary: We're looking for an experienced CQV Engineer who enjoys owning equipment projects from concept to production in a highly regulated pharmaceutical environment. Responsibilities:
South Plainfield, NJ · On-site
CQV Engineer Summary: We're looking for an experienced CQV Engineer who enjoys owning equipment projects from concept to production in a highly regulated pharmaceutical environment. Responsibilities:
Holly Springs, NC · On-site
CQV CIP engineer Holly Springs, NC Description: Need an entry to mid-level CQV CIP engineer with an intermediate level of understanding of Validation and Quality Assurance. Roles & Responsibilities:
Holly Springs, NC · On-site
CQV CIP engineer Holly Springs, NC Description: Need an entry to mid-level CQV CIP engineer with an intermediate level of understanding of Validation and Quality Assurance. Roles & Responsibilities:
Holly Springs, NC · On-site
CQV Engineer Location: Holly Springs, NC Duration: Long-Term Contract Summary: We are hiring experienced CQV Engineers for a large greenfield biopharmaceutical manufacturing project in Holly Springs ...
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Holly Springs, NC · On-site
CQV Engineer Location: Holly Springs, NC Duration: Long-Term Contract Summary: We are hiring experienced CQV Engineers for a large greenfield biopharmaceutical manufacturing project in Holly Springs ...
Bloomington, IN · On-site
CQV Engineer Location: Bloomington, IN (Onsite) Experience: 10+ Years (Pharma Required) Job Summary: Seeking an experienced CQV Engineer with 10+ years of pharmaceutical industry experience to ...
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Bloomington, IN · On-site
CQV Engineer Location: Bloomington, IN (Onsite) Experience: 10+ Years (Pharma Required) Job Summary: Seeking an experienced CQV Engineer with 10+ years of pharmaceutical industry experience to ...
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 ...
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 ...
Lexington, KY · On-site
Title: Validation Engineer (CQV) Location: Lexington, KY Onsite Duration: Long term Positions: 3 Job Summary We are seeking a Validation Engineer to support Commissioning, Qualification, and ...
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Lexington, KY · On-site
Title: Validation Engineer (CQV) Location: Lexington, KY Onsite Duration: Long term Positions: 3 Job Summary We are seeking a Validation Engineer to support Commissioning, Qualification, and ...
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 ...
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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 ...
Framingham, MA · On-site
CQV Specialist Location: Framingham, MA (Onsite) Duration: 6+ months Job Summary: The CQV Specialist will support commissioning, qualification, and validation activities for utilities, equipment, and ...
Quick apply
Framingham, MA · On-site
CQV Specialist Location: Framingham, MA (Onsite) Duration: 6+ months Job Summary: The CQV Specialist will support commissioning, qualification, and validation activities for utilities, equipment, and ...
Raritan, NJ · On-site
Job Title: Sr. CQV Specialist Location: Raritan, NJ Duration: Longterm Job Summary Sr. CQV Specialist needed to manage and execute Commissioning, Qualification, and Validation activities in a cGMP ...
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Raritan, NJ · On-site
Job Title: Sr. CQV Specialist Location: Raritan, NJ Duration: Longterm Job Summary Sr. CQV Specialist needed to manage and execute Commissioning, Qualification, and Validation activities in a cGMP ...
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 ...
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 ...
Charleston, WV · On-site
The CQV Associate Director, also known as a Discipline Lead (DL) is a recognized CQV subject matter expert, who can act in a project oversight role, to include managing client relationships for ...
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Charleston, WV · On-site
The CQV Associate Director, also known as a Discipline Lead (DL) is a recognized CQV subject matter expert, who can act in a project oversight role, to include managing client relationships for ...
Los Angeles, CA · On-site
This is Mahaboob from Intellectt INC; we've got an important CQV Consultant - Los Angeles, CA with one of our prestigious clients. Interested candidates can please send your updated resume at ...
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Los Angeles, CA · On-site
This is Mahaboob from Intellectt INC; we've got an important CQV Consultant - Los Angeles, CA with one of our prestigious clients. Interested candidates can please send your updated resume at ...
Cranbury, NJ · On-site
Job Title - Manager - SR Manager, CQV Quality Control Work Location - Cranbuy NJ Job Summary The Manager, CQV Quality Control is responsible for the strategic and operational leadership of QC CQV ...
Cranbury, NJ · On-site
Job Title - Manager - SR Manager, CQV Quality Control Work Location - Cranbuy NJ Job Summary The Manager, CQV Quality Control is responsible for the strategic and operational leadership of QC CQV ...
$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 ...
$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 ...
Conshohocken, PA · On-site
Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Philadelphia area Outsourced Technical Services(OTS) team in Philadelphia, PA . Outsourced ...
Conshohocken, PA · On-site
Overview The CQV Engineer III position is an exciting opportunity to join PM Group's quickly growing Philadelphia area Outsourced Technical Services(OTS) team in Philadelphia, PA . Outsourced ...
Raleigh, NC · On-site
CQV Engineer III CRB is a leading provider of sustainable Engineering, Architecture, Construction and Consulting solutions to the global life sciences and food and beverage industries. Our 1,200 ...
Raleigh, NC · On-site
CQV Engineer III CRB is a leading provider of sustainable Engineering, Architecture, Construction and Consulting solutions to the global life sciences and food and beverage industries. Our 1,200 ...
$91K - $96.1K
4% of jobs
$96.1K - $101.2K
5% of jobs
$101.2K - $106.3K
13% of jobs
$107.4K is the 25th percentile. Wages below this are outliers.
$106.3K - $111.4K
12% of jobs
$111.4K - $116.5K
12% of jobs
The median wage is $118.3K / yr.
$116.5K - $121.5K
12% of jobs
$121.5K - $126.6K
11% of jobs
$129.9K is the 75th percentile. Wages above this are outliers.
$126.6K - $131.7K
11% of jobs
$131.7K - $136.8K
15% of jobs
$136.8K - $141.9K
5% of jobs
$141.9K - $147K
1% of jobs
$91K
$120K
$147K
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.
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.
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.
Contractor
Posted 14 days ago
Job Title: CQV Engineer
Location: Philadelphia, PA
Duration: Long Term Contract
Job Summary
We are seeking a highly motivated CQV (Commissioning, Qualification, and Validation) Engineer to support commissioning and qualification activities within a GMP-regulated biopharmaceutical manufacturing environment. The CQV Engineer will be responsible for supporting equipment startup, system qualification, utility validation, and process readiness activities to ensure compliance with FDA, cGMP, and industry standards.
The ideal candidate will work closely with Engineering, Manufacturing, Quality Assurance, Validation, and Automation teams to support capital projects, facility expansion initiatives, and manufacturing operations.
Key Responsibilities
Required Qualifications
