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Equipment Cqv Engineer Jobs (NOW HIRING)

Position CQV Engineer Location North Carolina Duration Long Term Job Overview We are seeking a CQV ... Perform IQ, OQ, and PQ activities for equipment, utilities, and systems. * Support commissioning ...

Site Equipment & CQV Lead

Indianapolis, IN ยท On-site

$124K - $186K/yr

Responsible for leading the equipment and CQV engineering team at a GMP Radioligand Therapies Isotope Production Facility. Act as Equipment & CQV Workstream Lead on a major site capital project with ...

CQV Engineer Location: North Carolina Duration: Long Term Job Overview We are seeking a CQV ... Perform IQ, OQ, and PQ activities for equipment, utilities, and systems. * Support commissioning ...

CQV Engineer

Austin, TX ยท On-site

CQV Engineer Location: Austin, TX Duration: Long Term Position Overview We are seeking an ... This role will focus on equipment qualification, utility validation, process validation, and ...

The ideal candidate will provide technical leadership and field execution support for equipment and ... The CQV Engineer II will develop and implement commissioning strategies, lead verification ...

The ideal candidate will provide technical leadership and field execution support for equipment and ... The CQV Engineer II will develop and implement commissioning strategies, lead verification ...

CQV Engineer

Milano, TX ยท On-site

The CQV Engineer develops the documentation to support Commissioning, Qualifications, and ... Ideally, you will already have experience in facilities and equipment startup, walk downs ...

Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer ... Lead and execute equipment qualification and validation activities primarily for packaging systems ...

$70K - $115K/yr

Execute commissioning and qualification protocols in the field for GMP manufacturing equipment ... CQV, manufacturing, engineering, facilities, operations, quality, or another GMP technical role ...

New

Senior Packaging CQV Engineer Summary: We are seeking a Senior CQV / Packaging Validation Engineer ... Lead and execute equipment qualification and validation activities primarily for packaging systems ...

CQV ENGINEER

Thousand Oaks, CA ยท On-site

$70K - $115K/yr

Execute commissioning and qualification protocols in the field for GMP manufacturing equipment ... CQV, manufacturing, engineering, facilities, operations, quality, or another GMP technical role ...

New

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How much do equipment cqv engineer jobs pay per hour?

As of Sep 12, 2026, the average hourly pay for equipment cqv engineer in the United States is $63.77, according to ZipRecruiter salary data. Most workers in this role earn between $52.64 and $69.71 per hour, depending on experience, location, and employer.
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Equipment CQV Engineer

Boston, MA โ€ข On-site

Contractor

Posted 23 days ago


Job description

Equipment CQV Engineer 

Role: 

Seeking experienced Equipment CQV Engineers to support an onsite GMP equipment qualification program at a biopharmaceutical manufacturing facility. The role focuses on hands-on execution of equipment commissioning and qualification activities across manufacturing, laboratory, and support of equipment in a regulated GMP environment. 

Key Responsibilities: 

  • Review and execute established equipment qualification protocols (IQ/OQ). 

  • Document test results and identify/resolve execution issues. 

  • Support equipment readiness for manufacturing and engineering activities. 

  • Qualify various manufacturing, laboratory, and support equipment. 

  • Partner with Engineering, Validation, Manufacturing, Quality, and equipment vendors. 

  • Work independently, moving quickly through multiple equipment packages. 

Required: 

  • 5–10 years of CQV, equipment validation, or equipment qualification experience. 

  • Strong hands-on experience executing IQ/OQ and other equipment qualification protocols. 

  • Pharmaceutical, biotechnology, biopharmaceutical, cell therapy, or other GMP-regulated manufacturing experience. 

  • Experience qualifying for manufacturing and/or laboratory equipment. 

  • Ability to review protocols, execute testing, document results, and address discrepancies/deviations. 

  • Understanding GMP documentation and good documentation practices.