Beka Vite
About Beka Vite
Beka Vite is a Regulatory Manager at Teleflex with over a decade of experience in regulatory affairs within the medical device industry.
Title: Regulatory Manager at Teleflex
Beka Vite serves as the Regulatory Manager at Teleflex. This role builds on his extensive experience in regulatory affairs within the medical device industry. Prior to his current position, he was the Principal Regulatory Product Specialist at Teleflex from 2018 to 2021. Beka Vite's diverse background in regulatory roles equips him with the expertise needed to navigate complex regulatory landscapes effectively.
Previous Roles at Teleflex and Vascular Solutions
Beka Vite has a substantial history with Teleflex and its predecessor, Vascular Solutions. His previous positions include Senior Regulatory Product Specialist from 2016 to 2018 and Regulatory Product Specialist from 2014 to 2015 at Vascular Solutions. Additionally, he worked as Regulatory Operations Associate between 2013 and 2014. This progression reflects Beka Vite's deep regulatory knowledge and dedication to his profession.
Legal and Research Experience
Before his transition into regulatory roles, Beka Vite worked at William Mitchell College of Law as a Research Assistant from 2012 to 2013. He also served as a Forensic Law Clerk at Pathways Counseling Center from 2011 to 2013. These early roles in the legal and research fields provided him with valuable skills and insights that he later applied to his regulatory career in the medical device industry.
Education: J.D. and B.A.
Beka Vite earned his Juris Doctor (J.D.) degree from William Mitchell College of Law, where he studied from 2010 to 2013. Prior to that, he completed his Bachelor of Arts (B.A.) at Lawrence University, majoring in Biochemistry and Philosophy. This unique combination of legal and scientific education forms the foundation of his expertise in regulatory affairs.
Experience in Regulatory Affairs
Beka Vite has accumulated over a decade of experience in regulatory affairs within the medical device industry. His expertise spans regulatory operations and product specialization. This extensive experience has positioned him as a knowledgeable professional capable of addressing the intricate regulatory requirements faced by medical device companies.