**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 innovation, using technology and human genetic data to push beyond what’s known today.

**ABOUT THE ROLE**

**Role Description:**

This role is an individual contributor role that provides critical support to Product Quality Teams (PQTs) for late-stage clinical and commercial products. In this role, you will serve as a primary author of technical and regulatory reports, manage GMP data within compliant systems, and help ensure accuracy, completeness, and compliance across global submissions.

You will also play an integral role in maintaining Amgen’s electronic databases and mapping tools,...