Eugene Babcock
About Eugene Babcock
Eugene Babcock serves as the Associate Director of CMC Regulatory Affairs at ElevateBio, bringing extensive experience in regulatory affairs within the cell and gene therapy sectors. He has held various roles in prominent companies, including Kite Pharma and Amgen, and has advanced degrees in Regulatory Science and Biotechnology.
Work at ElevateBio
Eugene Babcock currently serves as the Associate Director of CMC Regulatory Affairs at ElevateBio, a position he has held since 2020. In this role, he focuses on regulatory affairs within the cell and gene therapy sectors. He has contributed to the establishment of BaseCamp, ElevateBio's centralized innovation and manufacturing center, which integrates capabilities across various cell and gene therapy platforms. His work supports the company's mission to advance innovative therapies.
Previous Experience in Regulatory Affairs
Before joining ElevateBio, Eugene Babcock held several positions in regulatory affairs. He worked at Kite Pharma as a Manager of Regulatory Affairs CMC from 2019 to 2020 and previously served as a Senior Specialist CMC at the same company from 2016 to 2019. His earlier experience includes roles at Shire, Baxalta, and Baxter International Inc., where he focused on quality control projects and regulatory compliance.
Education and Expertise
Eugene Babcock has a strong educational background in regulatory science and related fields. He earned a Doctor of Regulatory Science from the University of Southern California, completing his studies from 2020 to 2023. He also holds a Master of Science in Regulatory Science from the same institution. Additionally, he obtained a Bachelor of Science in Chemistry from the University of California, Irvine, and a Master of Science in Biotechnology and Bioinformatics from California State University Channel Islands. His expertise lies in regulatory affairs, particularly in cell and gene therapy and regenerative medicine.
Background in Research and Quality Control
Eugene Babcock has a background in research and quality control prior to his regulatory affairs career. He worked at Amgen, Inc. for five years, starting as a Research Associate and later becoming a Senior Research Associate. His experience also includes a position as a Principal Quality Laboratory Associate at Baxter International Inc. and roles in global quality control projects at Baxalta and Shire. This diverse experience has equipped him with a comprehensive understanding of the regulatory landscape.