CQV Engineer

Company

Katalyst Healthcares &amp; Life Sciences

Location

Los Angeles, California, United States

Type

Full-time

                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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