Description
Amgen is hiring an individual contributor to support Product Quality Teams for late-stage clinical and commercial products. The role involves authoring technical and regulatory reports, managing GMP data in compliant systems, maintaining electronic databases and mapping tools, supporting chromatographic overlay activities, and providing peer training. It requires a master’s degree and at least six years of pharmaceutical, biotechnology, quality, operations, scientific, or manufacturing experience, along with expertise in GMP systems, regulatory requirements, data management, and cross-functional collaboration.
