Manufacturing Quality Documentation Specialist

A pharmaceutical company in Vandalia, Ohio, is seeking a Specialist in Manufacturing Quality to support documentation and procedural activities related to non-conformances. This role involves minor OOS investigations, supporting Quality Systems, and ensuring compliance with FDA regulations. Candidates should have either an associate's degree with 3 years of manufacturing experience or a high school diploma with 5 years in the field. Skills in technical writing and proficiency in Microsoft Office are preferred. This position offers growth opportunities and a collaborative environment. #J-18808-Ljbffr