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CQV Engineer

Company

Katalyst Healthcares & Life Sciences

Location

Los Angeles, California, United States

Posted

May 15, 2026

Position Overview

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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