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Senior CQV Engineer

Job in Watertown, Middlesex County, Massachusetts, 02472, USA
Listing for: Meet Life Sciences
Full Time position
Listed on 2026-06-18
Job specializations:
  • Engineering
    Validation Engineer, Pharma Engineer, Quality Engineering, Biomedical Engineer
Salary/Wage Range or Industry Benchmark: 100000 - 125000 USD Yearly USD 100000.00 125000.00 YEAR
Job Description & How to Apply Below

The Senior CQV Engineer leads commissioning, qualification, and validation (CQV) activities for GMP manufacturing equipment, facilities, utilities, automation systems, and infrastructure
. This role ensures systems are designed, installed, tested, and maintained in compliance with cGMP and regulatory requirements while supporting capital projects, facility expansions, and operational readiness initiatives.

Responsibilities
  • Lead CQV activities for GMP equipment, utilities, facilities, automation systems, and infrastructure.
  • Develop and execute validation documentation, including plans, risk assessments, IQ/OQ/PQ protocols, traceability matrices, and summary reports.
  • Author, review, and approve SOPs, change controls, deviations, CAPAs, and validation lifecycle documents.
  • Coordinate commissioning, startup, and qualification activities to support project timelines and operational readiness.
  • Ensure compliance with cGMP, FDA, EU regulations, and data integrity requirements.
  • Collaborate with cross-functional teams (Engineering, Manufacturing, Quality, Automation, Process Development) and external vendors.
  • Support FATs, SATs, design reviews, construction walkdowns, and turnover documentation.
  • Participate in audits and regulatory inspections as needed.
  • Provide technical leadership, mentoring, and oversight to junior engineers and contractors.
  • Support continuous improvement initiatives, risk reduction, and CQV process optimization.
Qualifications
  • Bachelor’s degree in Engineering, Life Sciences, Biotechnology, Pharmaceutical Sciences, or related field required.
  • 6+ years of CQV experience in a GMP-regulated pharmaceutical, biotech, medical device, or life sciences environment.
  • Strong knowledge of cGMP, FDA, EU regulations, and validation lifecycle principles.
  • Experience leading CQV for GMP manufacturing equipment, utilities, facilities, and laboratory systems.
  • Proficiency in writing and executing validation deliverables (IQ/OQ/PQ, risk assessments, traceability matrices, etc.).
  • Experience supporting capital projects, equipment installations, and facility expansions.
  • Knowledge of CSV, automation systems, and data integrity requirements preferred.
  • Experience mentoring junior staff and collaborating across cross-functional teams.
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Position Requirements
10+ Years work experience
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