Jocelyn McQueen

Jocelyn McQueen is a regulatory affairs (RA) leader specializing in Chemistry, Manufacturing, and Controls (CMC) strategies and submissions within the biotechnology / pharmaceutical industry, with experience spanning drugs, biologics, biosimilars, and combination products. Jocelyn has been employed at Amgen, Inc., located in Thousand Oaks, CA, Singapore, and most recently Cambridge, MA, for 9 years this month working entirely within the Global RA CMC space, focusing on biological product Module 3 strategies and content for global clinical trial applications, marketing applications, and most prevalently, post approval variations. Though she has extensive product experience, one of Jocelyn’s greatest accomplishments at Amgen has been the development of her team of employees. Prior to Amgen, Jocelyn worked at Supernus Pharmaceuticals, Inc. in Rockville, MD for 5 years as an analytical chemist and in regulatory affairs. Jocelyn holds a Master’s degree in Bioscience Regulatory Affairs from the Johns Hopkins University (JHU) and a Bachelor of Science degree in Forensic Science from the University of Central Florida (UCF).