Document Control Manager

Reporting to the Director, Quality Management Systems, the Document Control Manager will focus on the creation, revision, management, and retirement of Quality Systems documents within the eDMS, and managing controlled records, including historical records, within the controlled library. Responsibilities: Facilitates the meticulous creation, revision, and retirement of controlled documents in the eDMS, including managing and tracking Document Change Control workflows and participants Management and migration of legacy files into the eQMS Coordinates with the Training Admin to create new or revisions to Training Requirements, learners, quizzes, and other training related to controlled documents Helps eDMS users with the how-to of document creation and revision and works with the QMS Admin to keep relevant document control SOPs and Work Instructions up to date Helps eDMS users find and use current effective documents Facilitates meetings with the QMS Admin and document reviewers to complete content creation or revisions Manages GxP record retention and destruction tasks Facilitates Certified Copy creation and retention Other duties as assigned. Qualifications: Bachelor’s degree in the life sciences, chemistry, or related field; or relevant experience Five plus (5+) years of experience in document control in a pharmaceutical company, or a related area Proficiency and experience with electronic document management systems, Veeva strongly preferred Knowledge of version control pra