Eric Elliott, Ms, Rac
About Eric Elliott, Ms, Rac
Eric Elliott is a Regulatory Affairs Manager II at Boston Scientific with extensive experience in regulatory leadership for endovascular medical devices.
Company History
Eric Elliott has built a distinguished career within the medical device industry, with substantial tenures at Boston Scientific and Medtronic. Eric is currently serving as Regulatory Affairs Manager II at Boston Scientific in the Greater Minneapolis-St. Paul Area, a role he has held since 2020. Prior to this, he served as Regulatory Affairs Manager at the same company from 2018 to 2020. His earlier role at Medtronic from 2016 to 2018 as Principal Regulatory Affairs - Neurovascular showcased his expertise in neurovascular devices in the Orange County, California Area. Eric also held various regulatory positions at Boston Scientific, including Principal Regulatory Affairs – PCI Guidance from 2011 to 2016 and Regulatory Affairs Specialist from 2006 to 2011.
Title and Role
Eric Elliott is currently the Regulatory Affairs Manager II at Boston Scientific. In this capacity, he focuses on providing regulatory leadership for the introduction of new endovascular medical devices. His role involves the development and execution of optimized global regulatory strategies for new product launches. With a career marked by substantial progression, Eric has demonstrated his abilities to manage project deliverables effectively within the regulatory affairs domain.
Education and Expertise
Eric Elliott holds a Master of Science (MS) in Clinical Trial Sciences from Rutgers University, which he completed between 2011 and 2014. Additionally, he earned a degree in Molecular Cellular and Developmental Biology from the University of Michigan from 2000 to 2006, where he also studied Material Science and Japanese Language. His educational background equips him with a robust foundation in both the scientific and regulatory aspects of the medical device industry.
Previous Experience
Before his current role, Eric Elliott has gathered extensive experience in various capacities. He worked as an Undergraduate Research Associate at the University of Michigan from 2004 to 2006 and as a Research & Development Co-op at the Kawamura Institute of Chemical Research in Chiba, Japan from 2003 to 2004. This diverse experience has contributed to his expertise in research and regulatory affairs.