Job Description:

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.

Requirements:

• Strong experience in CQV / Validation (IQ/OQ).


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