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🥝 CQV Engineer
Katalyst Healthcares & Life Sciences | Los Angeles, California, United States | Posted May 15, 2026
Job Description
Roles & Responsibilities:
- Lead qualification of cleanroom facilities and large-scale manufacturing process equipment, including centrifuges and filter presses
- Author, execute, and close validation protocols and final reports with minimal oversight
- Conduct construction walks, pre-check P&IDs, and identify, communicate, and escalate field and design issues
- Review and approve protocols, SOPs, TOPs, and vendor submittals against specifications and quality standards
- Drive execution planning, scheduling, and cross-functional coordination using DeltaV, Kneat, Veeva, Bluebeam, and MS365
Education & Experience:
- Bachelor's degree in engineering, Life Sciences, or a related field
- 3+ years of experience in validation within a regulated industry (e.g., pharma, biotech)
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