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Actalent

Quality Documentation Specialist II (GMP/GxP)

Actalent, Columbus, Ohio, United States, 43224

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A leading engineering and sciences services company is seeking a Quality Specialist II in Columbus, OH. This role is responsible for managing quality documentation and addressing issues in a regulated laboratory environment. An ideal candidate has a Bachelor's degree and 2-3 years of relevant experience, preferably in GMP or FDA settings. The position offers a competitive pay rate of $28/hour and requires onsite presence. #J-18808-Ljbffr