QA Specialist- Document Management System DMS Tech Writing Operations Support What you will do Let s do this Let s change the world In this vital role you will be responsible for supporting key strategic initiatives assigned tasks and or projects necessary to Amgen s strategic mission and departmental goals including the following activities Support optimization and maintenance of the DMS process including updates to the procedure the system CDOCS and associated training materials Maintain and enhance DMS document templates and authoring standards to ensure consistency and compliance Lead tech writing tasks in support of process and document simplification efforts Create update and deliver training materials for document owners reviewers and approvers on positive Quality writing per our document hierarchy and document authoring standards Update optimize and maintain the CDOCS support portal SharePoint - including training links e-Learnings Quick Reference Guides and other related materials Support of Document Management Network - maintenance of meetings Teams channel inspection readiness materials etc Management of DMS-related suppliers including periodic monitoring and quality agreement management Provide additional operational support for DMS activities as needed Basic Qualifications Doctorate degree and x years of Quality R D and or Manufacturing experience Or Master s degree and x years of Quality R D and or Manufacturing experience Or Bachelor s degree and x years of Quality R D and or Manufacturing experience Or Associate s degree and x years of Quality R D and or Manufacturing experience Or High school diploma GED and x years of Quality R D and or Manufacturing experience Prior technical writing experience in a regulated space Superior proficiency in English grammar syntax and style Preferred Qualifications Prior experience in the regulated document management space Experience in developing and delivering training programs or educational materials Ability to effectively communicate complex information to diverse audiences Understanding of global regulatory requirements affecting the Pharma Biotech sector Excellent project management skills with the ability to manage multiple initiatives simultaneously