This is a fast-paced opportunity focused purely on execution of validation protocols ideal for professionals who thrive on the manufacturing floor. We are looking for hands-on CQV Engineers to support a high-impact biologics project within a GMP-regulated environment.
Numbers & Facts
Location
Devens, MA
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