Job Description

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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