Ceira Olson

Ceira Olson has a robust background in regulatory affairs and quality engineering, with extensive experience in the medical device industry. From June 2018 to April 2023, Ceira served as a Senior Regulatory Affairs Specialist at Stryker, following previous roles as a Regulatory Affairs Specialist, Quality Engineer, and Quality System Specialist at the same company. Ceira also worked as a Quality Engineer at TELA Bio from September 2021 to January 2022 and gained experience as a Quality Assurance Engineer Co-op at K2M from January 2017 to April 2018. An internship with the FDA in 2016 involved research in the Medical Ultrasound lab focusing on tissue mimicking materials. Ceira holds a Bachelor of Science in Bioengineering and Biomedical Engineering, as well as a Bachelor of Science in Exercise Science with a minor in Chemistry, both from The University of Toledo.