Vacaville, California
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Yesterday
Position Summary We are seeking a Senior Commissioning, Qualification, and Validation (CQV) Engineer to support pharmaceutical and biopharmaceutical manufacturing projects. The ideal candidate has strong hands-on experience with upstream and downstream process equipment, including qualification planning, protocol development, field execution, and troubleshooting. Clean-in-Place (CIP) and Steam-in-Place (SIP) experience is a major plus. Key Responsibilities * Lead CQV activities for manufacturing
Easy Apply
Contract
55 - 60
