CIP CQV Engineer for Biopharma Validation
$87.78k - $136.23kVerista
A leading life sciences company located in Apex, NC, is seeking a CQV Engineer to support commissioning, qualification, and validation activities for Clean-in-Place (CIP) systems. The ideal candidate will have a Bachelor’s degree in Engineering or Life Sciences and hands-on experience in GMP-regulated environments. Key responsibilities include authoring CQV documentation and collaborating cross-functionally to ensure successful project execution. Competitive salary and benefits offered, with a range from $87,780 to $136,225 USD annually. #J-18808-Ljbffr Verista
Vacancy posted 2 days ago
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