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CSV Engineer II: GMP & FDA Validation Lead

A biotechnology company is seeking a meticulous CSV Engineer in San Diego, California. You will be responsible for ensuring that computerized systems in the biopharma industry comply with regulatory requirements. This includes developing and executing validation protocols, and collaborating with teams to define user requirements. The ideal candidate has a Bachelor's degree and 2+ years of experience in a regulated environment. Join a mission-driven team dedicated to transforming patient lives through innovative therapies. J-18808-Ljbffr

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