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CQV Engineer

Job

Katalyst Healthcares and Lifesciences

Devens, MA (In Person)

Full-Time

Posted 4 days ago (Updated 6 hours ago) • Actively hiring

Expires 6/11/2026

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Job Description

Summary :
We are looking for hands-on CQV Engineers to support a high-impact biologics project within a GMP-regulated environment. This is a fast-paced opportunity focused purely on execution of validation protocols-ideal for professionals who thrive on the manufacturing floor.
Roles & Responsibilities:
Execute IQ/OQ protocols for process equipment Perform equipment walkdowns and verify against design Support SIP/CIP cycles, wet testing, and temperature mapping Work with downstream equipment (chromatography, filtration, tank farms, etc.) Document and execute validation activities in ValGenesis Collaborate with QA/QC and Manufacturing teams
Education & Experience :
Strong experience in CQV / Validation (IQ/OQ) Background in biologics / biopharma / cell culture Hands-on experience with process equipment validation Familiarity with
GMP & GDP
practices Experience with downstream equipment

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