Eric L. Berg Amgen Inc.

Eric Berg's career in biopharmaceuticals spans 30+ years in Amgen Operations and includes roles within Manufacturing, Project Management, and Quality. He currently serves as Interim Quality Site Head, Manufacturing and Clinical Supply (Thousand Oaks, CA).

Eric started on the night shift in Drug Substance Clinical Manufacturing.  While in Manufacturing, he became a people manager, contributed to GMP facility start-ups, new product introductions, and hundreds of GMP batches. In Project Management, Eric delivered multi-site Quality System improvements, was Chief of Staff to the Global Quality VP, and led the Corporate Quality Project Management Office. Eric led Amgen's Corporate Supplier Quality Management team for 7 years during a period of significant transformation. Eric served as Quality lead for the Dún Laoghaire, Ireland site expansion to construct, commission, and start a syringe filling and packaging facility.  He has served as lead for Commercial Drug Product QA, Incoming Materials QA, Quality Systems, and Clinical and Commercial Drug Substance operations.

Eric holds a degree in Biological Sciences from California Lutheran University, became a certified PMP, and developed via the Deming Institute, Aikiworks with Tom Crum, and PDA. Currently Eric serves on the Rx-360 Board of Directors.  He is a member of the SoCal PDA Chapter.