Curtis Bordwell
About Curtis Bordwell
Curtis Bordwell is an Associate Director at Abeona Therapeutics, where he has worked since 2021. He has over a decade of experience in laboratory compliance and has held various positions in the biotechnology and pharmaceutical industries.
Current Role at Abeona Therapeutics
Curtis Bordwell serves as the Associate Director at Abeona Therapeutics, a position he has held since 2021. In this role, he is responsible for overseeing various aspects of the company's operations, ensuring that projects align with regulatory standards and organizational goals. His extensive experience in the biopharmaceutical sector contributes to his effectiveness in this leadership position.
Previous Experience at Abeona Therapeutics
Curtis Bordwell has held multiple positions at Abeona Therapeutics. He worked as a Senior Assay Development Associate from 2018 to 2020, where he focused on assay development processes. He later served as QC Manager for 9 months in 2020, managing quality control operations. Additionally, he worked as an Associate Scientist for 9 months in 2020, contributing to scientific research and development initiatives.
Experience at Ricerca Biosciences
Prior to his tenure at Abeona Therapeutics, Curtis Bordwell worked at Ricerca Biosciences as a Study Director and Associate Scientist II from 2013 to 2015. In this capacity, he directed studies and contributed to scientific research, enhancing his expertise in laboratory management and project oversight.
Background in Pharmaceutical Microbiology
Curtis Bordwell began his career at Boehringer Ingelheim, where he worked as a Pharmaceutical Microbiologist from 2010 to 2013. This role provided him with foundational knowledge in microbiological practices within the pharmaceutical industry, which he has built upon throughout his career.
Education and Expertise
Curtis Bordwell studied at The University of Akron, earning a Bachelor of Science (BS) in Biology/Biological Sciences from 2005 to 2010. He also attended Cuyahoga Community College, where he completed courses in Medical Terminology, Physics, and Human Anatomy and Physiology. His educational background supports his expertise in cGMP and GLP practices, as well as compliance with FDA, EMA, and EPA regulations in laboratory settings.