Quality Documentation Specialist I (QMS Focus)

A leading biotech firm located in Bedford, MA is seeking a QA Documentation Specialist I to maintain and manage Quality Management System documentation. Candidates should possess a high school diploma and have 2-5 years of experience in a cGMP regulated environment. Key responsibilities include issuing batch records, ensuring compliance, and supporting audits. The position demands strong organizational skills, attention to detail, and the ability to work independently. Comprehensive benefits including a 401(k) match, stock options, and generous paid time off are provided. #J-18808-Ljbffr