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Cqv Engineer Jobs (NOW HIRING)

Intellectt INC

CQV Engineer

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 ...

Intellectt INC

CQV Engineer

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 ...

Intellectt INC

CQV Engineer

Holly Springs, NC · On-site

CQV Engineer Location: Holly Springs, NC We are seeking an experienced CQV Engineer to support a large greenfield biopharmaceutical manufacturing project. The ideal candidate will have strong hands ...

Intellectt INC

CQV Engineer

Holly Springs, NC · On-site

CQV Engineer Location: Holly Springs, NC Job Summary Seeking experienced CQV Engineers to support a large greenfield biopharmaceutical manufacturing project. Candidates should have strong hands-on ...

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 ...

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 ...

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 ...

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 ...

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Cqv Engineer information

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How much do cqv engineer jobs pay per year?

As of Aug 1, 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 does a CQV engineer do?

A CQV (Commissioning, Qualification, and Validation) engineer is responsible for ensuring that manufacturing equipment, systems, and processes in industries like pharmaceuticals and biotech meet regulatory standards and quality requirements. They develop protocols, perform testing, and document procedures to validate that systems operate correctly and consistently. CQV engineers often work closely with project teams, utilize validation tools, and hold certifications such as GxP or cGMP compliance knowledge.

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.

What engineers make $300,000 a year?

Senior engineers in specialized fields such as petroleum, aerospace, or software engineering can earn $300,000 or more annually, especially with extensive experience, advanced skills, and often in leadership or executive roles. High compensation may also include bonuses, stock options, or other incentives, particularly in competitive industries or companies.

What is a CQV Engineer job?

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 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.

What are the key skills and qualifications needed to thrive in the Cqv Engineer position, and why are they important?

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 engineer makes $500,000 a year?

Highly experienced engineers in specialized fields such as petroleum engineering, aerospace engineering, or certain senior roles in software engineering can earn $500,000 or more annually, often including bonuses and stock options. Achieving this level typically requires advanced skills, extensive experience, and working in high-paying industries or leadership positions.
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Cqv Engineer jobs near you
Infographic showing various Cqv Engineer job openings in the United States as of July 2026, with employment types broken down into 12% Internship, 6% As Needed, 19% Full Time, 39% Temporary, 1% Contract, and 23% Nights. Highlights an 89% Physical, 3% Hybrid, and 8% Remote job distribution, with an average salary of $89,183 per year, or $42.9 per hour.

CQV Engineer

Intellectt INC

Bloomington, IN • On-site

Contractor

Re-posted 20 days ago

Job description

Hello,

I hope you’re doing well.

My name is Vyshu, and I’m reaching out from Intellectt Inc. regarding an exciting contract opportunity for CQV Engineer based in Bloomington, IN with one of our prestigious clients.

I would love to connect and discuss this opportunity in more detail. Please feel free to share your updated resume at vyshnavi.t@intellectt.com

Job Title: 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 support a CDMO client in Bloomington, IN. The ideal candidate will have strong expertise in commissioning, qualification, and validation of large-scale manufacturing equipment.

Key Responsibilities:

  • Develop and execute CQV documentation (IQ/OQ/PQ protocols, reports).
  • Support commissioning and qualification of manufacturing equipment.
  • Work with fill/finish lines and lyophilizers.
  • Ensure compliance with GMP and regulatory standards.
  • Coordinate with cross-functional teams to meet project timelines.

Requirements:

  • 10+ years of CQV experience in pharmaceutical manufacturing.
  • Hands-on experience with fill/finish equipment and lyophilizers.
  • Strong documentation and execution skills.
  • CDMO experience preferred.

Thanks & Regards,
Vyshnavi
Recruiter
Intellectt Inc 
vyshnavi.t@intellectt.com
Direct: 732 204 6550
Desk number: 732 412 6999 - Ext: 225