CQV Engineer
Job in
Atlanta, Fulton County, Georgia, 31199, USA
Listed on 2026-09-25
Listing for:
Katalyst Healthcares & Life Sciences
Full Time
position Listed on 2026-09-25
Job specializations:
-
Engineering
Validation Engineer, Pharma Engineer, Quality Engineering, Biomedical Engineer
Job Description & How to Apply Below
26-01612
Summary:
Seeking a CQV Validation Engineer with 5+ years of experience in pharmaceutical, biotech, or life sciences. The ideal candidate will have hands-on experience with Commissioning, Qualification & Validation (CQV) for standalone manufacturing equipment in a GMP-regulated environment.
Roles & Responsibilities :
Perform CQV activities for standalone equipment. Author and execute IQ/OQ/PQ protocols, validation plans, and reports. Support FAT, SAT, commissioning, qualification, and validation activities. Perform risk assessments and support deviations, CAPA, and change control. Review vendor documentation, equipment manuals, and engineering drawings. Ensure compliance with FDA, cGMP, GAMP 5, and 21 CFR Part 11.
Education & Experience:
5+ years of CQV validation experience in Pharma/Biotech. Strong experience with standalone equipment qualification. Hands-on experience with IQ/OQ/PQ protocol authoring and execution. Knowledge of FDA, cGMP, GAMP 5, ISPE, and 21 CFR Part 11. Preferred Equipment Autoclaves, Washers, Bioreactors, Mixers, Tanks & Vessels, CIP/SIP Systems, Process Skids, Filling Equipment, Packaging Equipment, Incubators, and Freezers.
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