Laura Jones

Laura Jones has an extensive work history in the quality assurance and regulatory affairs field. Laura is currently the Vice President of Quality and Regulatory Affairs at Biogennix since 2022. Prior to that, they served as the Head of Quality at Cedars-Sinai from 2021 to 2022. Laura has also worked at ThermoFisher as a Product Quality specialist from 2019 to 2020, and as the Global Director of Quality and Regulatory Affairs at Eurofins from 2019 to 2019. Before that, Laura held positions at Endologix Inc as a Quality Fellow and Principal Design Assurance Engineer from 2014 to 2019. Laura was also the Vice President of Quality and Regulatory Affairs at Avrio Biopharmaceuticals from 2012 to 2014. Laura has experience at Bayer HealthCare, Valeant Pharmaceuticals Intl Inc/Dow Pharmaceuticals, Medtronic Spine & Biologics/Kyphon, and Cardinal Health, Inc. with various roles in quality assurance and regulatory affairs.

Laura Jones has pursued a diverse and extensive education history, with focuses on regulatory affairs, law, microbiology, and management/marketing. Laura obtained a Master of Science (M.S.) degree in Regulatory Affairs from San Diego State University and a Juris Doctor (J.D.) degree in Law from the American College of Law. In addition, Laura earned a Ph.D. in Microbiology from Louisiana State University and an MBA in Management/Marketing from the University of Wisconsin-Madison. The specific years and durations for each educational experience are not provided.