Lisa Erickson
About Lisa Erickson
Lisa Erickson is a Senior Director at Beigene in Cambridge, Massachusetts, with over 30 years of experience in the biopharmaceutical industry, particularly in regulatory affairs and chemistry manufacturing and controls (CMC).
Current Role at Beigene
Lisa Erickson serves as the Senior Director at Beigene in Cambridge, Massachusetts, United States. In addition, she is also the Director of CMC Regulatory Affairs at the same location. Her work focuses on regulatory strategies and compliance within the biopharmaceutical industry, emphasizing Chemistry, Manufacturing, and Controls (CMC).
Previous Experience at Medivation
From 2015 to 2017, Lisa Erickson worked at Medivation in New York, New York, United States, as Regulatory Affairs CMC. Her role involved managing regulatory affairs for oncology products, ensuring compliance with industry standards and regulatory requirements.
Consulting Roles
Between 2012 and 2015, Lisa Erickson held consulting positions. She was the Principal Consultant, CMC at Regsource Consulting Inc. in Cary, North Carolina. Additionally, she worked as an Independent Regulatory Consultant, taking the role of Principal. During these years, she provided expert advice on regulatory strategies for biopharmaceutical companies.
Long Tenure at Amgen
Lisa Erickson's career at Amgen spanned over two decades, from 1988 to 2011. She held various roles including Senior Manager of Regulatory Affairs CMC, CMC Operations and Compliance, and QC Stability. Her significant contributions included playing a crucial role in the regulatory submissions and approvals for multiple biopharmaceutical products.
Educational Background
Lisa Erickson earned her Bachelor of Science degree in Biochemistry and Physiology from the University of California, Davis. She studied from 1983 to 1987, gaining foundational knowledge that would support her extensive career in the biopharmaceutical industry.