10 Zimmer Biomet regulatory affairs leaders
VP Regulatory Affairs, Quality and Regulatory Affairs Director, Americas and Director of Regulatory Affairs are among the roles held by these ten Zimmer Biomet regulatory affairs leaders, some of whom have since moved on. A reader can learn how regulatory affairs leaders work at Zimmer Biomet from people who have held the role.
Professionals to explore
Adrian Atherton, Ph.D.
LinkedInExperience: Quality & Regulatory Affairs Director · Zimmer Biomet
Adrian Atherton has been Quality & Regulatory Affairs Director at Zimmer Biomet since August 2026, based in Fallbrook, California. Adrian Atherton was Sr. Director, Quality & Regulatory at Pacira BioSciences, Inc. from 2024 to 2026 and Head of Quality and Regulatory at Innova Medical Group from 2023 to 2024.
David Kunz
LinkedInExperience: Senior Vice President, Global Quality and Regulatory Affairs · Zimmer Biomet
David Kunz has been Senior Vice President, Global Quality and Regulatory Affairs at Zimmer Biomet since January 2017, based in St Paul, Minnesota. At Zimmer Biomet, David Kunz was Vice President, Global Quality, Regulatory, and Clinical Affairs from 2015 to 2017 and Vice President, Quality & Regulatory Affairs from 2012 to 2015.
Dottie Snyder
LinkedInExperience: Former Director Regulatory Affairs · Zimmer Biomet
Dottie Snyder is a former Director Regulatory Affairs at Zimmer Biomet, a role the profile lists from 1999 to 2023, based in Warsaw, Indiana, and the profile headline reads Director Regulatory Affairs. The listing shows no other roles on the profile, so check the full profile for the rest of the background.
Hema Bhatt
LinkedInExperience: Director - Regulatory Affairs & Quality · Zimmer of Canada
Hema Bhatt has been Director - Regulatory Affairs & Quality at Zimmer of Canada since 2007, based in Mississauga, Ontario. Hema Bhatt was Regulatory Affairs Specialist at Baylis Medical Company Inc., Mississauga, ON from 2005 to 2007 and Regulatory Affairs Associate at CanReg from 2004 to 2005.
Juan D Buitrago
LinkedInExperience: Quality and Regulatory Affairs Director, Americas · Zimmer Biomet
Juan D Buitrago has been Quality and Regulatory Affairs Director, Americas at Zimmer Biomet since January 2024, based in Naperville, Illinois. At Zimmer Biomet, Juan D Buitrago was Director of Regulatory Affairs, Corporate and Americas from 2021 to 2024, Director, Global RA Corporate Services from 2019 to 2021 and Regulatory Affairs Director Americas (Latin America & Canada) from 2017 to 2019.
Lea Atallah
LinkedInExperience: EMEA Director, Quality Commercial, Regulatory Affairs, & Global Supply Chain Center · Zimmer Biomet
Lea Atallah has been EMEA Director, Quality Commercial, Regulatory Affairs, & Global Supply Chain Center at Zimmer Biomet since June 2026, based in the United Arab Emirates. At Zimmer Biomet, Lea Atallah was Associate Director, Quality & Regulatory Affairs from 2022 to 2026 and Manager, Quality & Regulatory Affairs from 2016 to 2021.
Rebecca Noftz
LinkedInExperience: Former Director of Regulatory Affairs · Zimmer Biomet
Rebecca Noftz is a former Director of Regulatory Affairs at Zimmer Biomet, a role held from 2021 to 2026, and has been a Director at Stryker since March 2026. At Zimmer Biomet, Rebecca Noftz was Regulatory Affairs Associate Director, Hips from 2018 to 2021 and Regulatory Affairs Manager, Extremities from 2014 to 2018.
Renee Borgesano
LinkedInExperience: Director of Regulatory Affairs · Zimmer Biomet
Renee Borgesano has been Director of Regulatory Affairs at Zimmer Biomet since September 2022, based in North Haven, Connecticut. Renee Borgesano was Director of Regulatory Affairs at Hologic, Inc. from 2021 to 2022, Senior Manager Regulatory Affairs at Hologic from 2019 to 2021 and Director (Associate) of Regulatory Affairs at Medtronic from 2014 to 2019.
Ted Kuhn
LinkedInExperience: Former Director of Regulatory Affairs · Zimmer Biomet
Ted Kuhn is a former Director of Regulatory Affairs at Zimmer Biomet, a role held from 2019 to 2021, and the profile headline places the role at Zimmer Biomet Spine and OBT. At Zimmer Biomet, Ted Kuhn was Associate Director, Regulatory Affairs from 2017 to 2019 and Regulatory Affairs Project Manager from 2014 to 2017.
Choose the right perspective
Match the scope in a person's title, such as global, a region like the Americas or EMEA, or combined quality and regulatory work, to the question you need answered. Weigh how recent a person's time in the role is against how close their past work sits to your decision.
Questions to take into the conversation
- 01What did you focus on first when you took on your regulatory affairs role at Zimmer Biomet?
- 02Which regulatory affairs decision at Zimmer Biomet would you make differently today, and why?
- 03What has your own work taught you about running regulatory affairs alongside quality in a device company?
Reaching Zimmer Biomet regulatory affairs leaders
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Pick one of the 10 people on this page and choose "Book a paid call", or describe your project to find others. You offer a fee for a 15-minute call or a written answer, Instant Expert finds the person's work email and sends the invitation, and they decide whether to accept. The list covers 2 companies: Zimmer Biomet and Zimmer of Canada, based on profile data retrieved on October 25, 2026. Being listed here doesn't mean someone has agreed to take calls.
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About this directory
This is a professional research starting point based on business profile data retrieved on . Titles and companies reflect that source snapshot; roles marked former had ended by then. Check the linked profiles for current details. Inclusion does not imply Instant Expert membership or availability.