Role Overview
Independently author routine to moderately complex regulatory documents, manage document versions, reviewer comments, and approval workflows end-to-end for assigned documents, and ensure assigned documents are scientifically accurate, internally consistent, and aligned with source data and program objectives.
About Amgen
Amgen harnesses the best of biology and technology to fight the world’s toughest diseases, and make people’s lives easier, fuller and longer. We discover, develop, manufacture and deliver innovative medicines to help millions of patients. Amgen helped establish the biotechnology industry more than 40 years ago and remains on the cutting-edge of inn