Job Description
Job Summary
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 commi...
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Submit ApplicationJob Details
- Location watertown, ma
- Job Type Full-time
- Category Pharmaceutical Manufacturing
- Posted Date June 19, 2026
- Application Deadline July 29, 2026