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Kim Rendon has over 20 years of experience in Regulatory Affairs. Kim began their career in 1992 as a Regulatory Affairs Analyst at Nobel Biocare (Formerly Steri-Oss). Kim then worked as a Regulatory Affairs Associate at Edwards Lifesciences in 1999, followed by a role as Regulatory Affairs Specialist at Radiance Medical Systems (now Endologix) in 2000. In 2001, they worked as a RA Consultant at Triage Medical. From 2005 to 2021, they held various roles at Siemens Healthineers, including Director of Regulatory Affairs, NAM, Manager, Regulatory and Clinical Affairs, and Regulatory Affairs Specialist (U. S. Submissions for FDA Class II and Class III imaging devices, including mammography, urology, lithotripsy, surgery (C-Arms), mobile x-ray). In 2021, they began their current role as Director, Regulatory Affairs at Proscia.

Kim Rendon attended the University of Scranton from 1985 to 1989, where they earned a Bachelor of Science degree in International Studies/Business.