Susan Bechler is a Regulatory Affairs Sr. Specialist at Arthrex since August 2021, with a robust background in regulatory affairs and quality assurance spanning over 15 years. Prior experience includes roles as RA/QA Associate Manager and Regulatory Affairs Specialist at Zimmer Biomet, where responsibilities included serving as a local point-of-contact for the Asia Pacific region and managing regulatory submissions and maintenance. Additionally, Susan worked at Biomet as an International Regulatory Affairs Specialist, handling device dossiers and compliance in both Australia and Canada, and ensuring adherence to EU regulations through preparation of technical files and design dossier submissions. Susan earned a Bachelor of Arts in Telecommunications from Indiana University Bloomington in 1996.
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