|Zimmer||Vice-président QA/RARA EMEA||Germany|
| How does MDR impact your regulatory planning? |
Mr. Buerger is the Vice President Regulatory Affairs and Quality Assurance EMEA for Zimmer Biomet. He has a Master’s of Science degree in Biomedical Engineering from Marquette University in Milwaukee, WI, as well as a Dipl. Ing. degree in Electrical Engineering from Fachhochschule Dieburg in Germany. In the past Mr. Buerger has had a variety of different management roles in QA and Regulatory Affairs for companies including GE, Baxter, Terumo & Guidant. He has also worked as a Quality Management Systems and Operational consultant for Grant-Thornton, as well as spending time as a lead auditor and test engineer for TUV Rheinland, a European Notified Body.
Mr. Buerger has spoken at a variety of international conferences, including RAPS, MD&D, ASQ, IEEE and others.