Lisa Owens
About Lisa Owens
Lisa Owens is the Director of Regulatory Operations at BeiGene in San Mateo, California, with over 20 years of experience in regulatory operations and project management within the pharmaceutical and biotechnology industries.
Title and Current Role
Lisa Owens is the Director of Regulatory Operations at BeiGene in San Mateo, California, United States. In this role, she is responsible for overseeing regulatory submissions and ensuring compliance with regulatory requirements in the pharmaceutical and biotechnology industries.
Previous Experience at Gilead Sciences
Lisa Owens worked at Gilead Sciences in various significant roles over a span of more than five years. She served as Associate Director of Regulatory Operations from 2016 to 2017 in Cambridge, UK. Prior to this, she held the positions of Senior Manager of Regulatory Operations from 2012 to 2015 and Manager of Regulatory Project Management in 2012, both in Cambridge and Foster City, UK. Additionally, she was Regulatory Operations Manager from 2011 to 2012.
Educational Background
Lisa Owens has an extensive educational background. She attained a Master of Business Administration (MBA) from the Paul Merage School of Business, University of California, Irvine, between 2008 and 2010. She also studied Leadership and Management at Chapman University in 2008 and attended UC San Diego during the same year. Additionally, she earned a Bachelor of Arts in Political Science and Government from San Diego State University after six years of study from 1997 to 2003.
Experience in Regulatory Operations
With over 20 years of experience in regulatory operations and project management within the pharmaceutical and biotechnology industries, Lisa Owens has held various key roles. She has worked as a Regulatory Publishing Manager at Allergan in 2010 and earlier as a Regulatory Publishing Specialist from 2006 to 2010. Her career also includes positions as Regulatory Operations Lead at ISTA Pharmaceuticals and Regulatory Electronic Submission Consultant at companies like Halozyme Therapeutics and Maxim Pharmaceuticals.
Regulatory Submission Expertise
Throughout her career, Lisa Owens has played a key role in the regulatory submission processes for multiple high-profile pharmaceutical companies, including Gilead Sciences and Allergan. She has extensive experience in managing regulatory publishing and electronic submissions, having worked in various capacities from specialist to director level. Her contributions include the successful regulatory approval of several major pharmaceutical products.