Regulatory Documentation Specialist

A leading manufacturing firm located in Warwick, RI, is seeking a Documentation Coordinator to manage quality documentation in compliance with FDA regulations. This role ensures data integrity and product quality, particularly for OTC products, through detailed batch record review, audit support, and maintaining inspection-ready documentation. Applicants should have a degree in Quality or a related field and 2-5 years of experience in document control within an FDA-regulated environment. #J-18808-Ljbffr