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) ...