What are the responsibilities and job description for the CQV Engineer position at Katalyst Healthcares and Lifesciences?
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:
Education & Experience :
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
- Familiarity with GMP & GDP practices
- Experience with downstream equipment