QA Specialist I, Document Control

The QA Specialist I, Document Control serves as the accountable owner of the GMP Document Control program for the Canton, MA vaccine Drug Substance manufacturing site, ensuring compliance with US FDA regulations and global standards. This role involves managing the end-to-end governance, execution, and continuous improvement of document and records management processes while serving as the site subject matter expert for the Electronic Document Management System. The position requires partnering with global stakeholders and site leadership to maintain inspection-ready operations and drive data integrity across the document lifecycle.