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Equipment Qualification Engineer Cqv Jobs (NOW HIRING)

Centstone

Validation Engineer (CQV)

Lexington, KY · On-site

Validation Engineer (CQV) Location: Lexington, KY Onsite Duration: Long term Positions: 3 Job ... Qualification, and Validation (CQV) activities for utilities, process equipment, and process ...

Stark Pharma Solutions Inc

CQV Engineer

Austin, TX · 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 ...

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How much do equipment qualification engineer cqv jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for equipment qualification engineer cqv 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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Infographic showing various Equipment Qualification Engineer Cqv job openings in the United States as of June 2026, with employment types broken down into 6% As Needed, 89% Part Time, 1% Contract, and 4% Nights. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $132,650 per year, or $63.8 per hour.

Equipment Qualification Engineer

Summit, NJ • On-site

Prophecy Technologies
Professional, Scientific, and Technical Services • 11 - 50 employees
Learn more about Prophecy Technologiesexternal

Full-time

Re-posted 10 days ago

Job description

Role Overview:
We are seeking an experienced Equipment Qualification Engineer to support equipment qualification activities at a Summit, New Jersey site. The ideal candidate will have hands-on experience executing qualification lifecycle activities for GMP-regulated manufacturing or laboratory equipment and possess a strong understanding of validation and qualification requirements within the pharmaceutical, biotechnology, or life sciences industry.
Key Responsibilities:
  • Execute equipment qualification activities, including IQ, OQ, PQ, and requalification.
  • Prepare, review, and execute qualification protocols and reports.
  • Support commissioning, qualification, and validation activities for manufacturing and laboratory equipment.
  • Collaborate with Engineering, Manufacturing, Quality Assurance, and Validation teams to ensure timely project execution.
  • Review and assess vendor documentation, including FAT/SAT documentation and qualification packages.
  • Support deviation investigations, change controls, and CAPA activities associated with equipment qualification.
  • Ensure compliance with GMP, GDP, and applicable regulatory requirements.
  • Maintain qualification documentation and provide support during inspections and audits.

Required Skills:
  • Strong experience with qualification lifecycle documentation (URS, DQ, IQ, OQ, PQ, FAT, SAT).
  • Familiarity with GMP regulations and validation principles.
  • Experience working in manufacturing, laboratory, or cell therapy environments.
  • Excellent documentation, communication, and stakeholder management skills.

Qualifications:
  • Bachelors degree in Engineering, Life Sciences, Pharmacy, or a related discipline.
  • Minimum 5+ years of experience in Equipment Qualification within the pharmaceutical, biotechnology, or medical device industry.

Preferred Skills:
  • Prior experience qualifying bioprocessing and cell therapy manufacturing equipment.
  • Experience with Cytiva Sepax equipment is highly desirable.
  • Experience supporting commissioning and startup activities for new equipment installations.
  • Knowledge of data integrity and computerized system interfaces associated with equipment.
  • Hands-on experience with Cytiva Sepax Cell Processing Systems will be considered a significant advantage.

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