QA Documentation & Control Specialist

A leading contract research organization is seeking a QA Documentation Specialist in Branchburg, NJ. The role involves managing documentation changes within the electronic document management system, ensuring compliance with regulatory requirements, and coordinating the review of documents. Candidates should hold a bachelor's degree in a relevant field and have at least 3 years of experience in quality assurance in the pharmaceutical or medical device industry. Proficiency in Microsoft Word, Excel, and eDMS experience is preferred. This is a full-time mid-senior level position. #J-18808-Ljbffr