Senior CQV Engineer
Job in
Watertown, Middlesex County, Massachusetts, 02472, USA
Listed on 2026-06-18
Listing for:
Meet Life Sciences
Full Time
position Listed on 2026-06-18
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Biomedical Engineer
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.
- 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.
- 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.
Position Requirements
10+ Years
work experience
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