A BDN client is looking for a strong EU MDR Regulatory Consultant to come in and help convert existing tech files to the new EU MDR. There are some existing tech files from the Netherlands that will need to be “re-created” to meet the new EU standards. The candidate will have to work well within a team as they have sites/manufacturers throughout the United States and the EU that they will have to conference with. The devices are mostly Class II-III according to EU MDR. This individual should have a strong MDD experience and knowledge of EU MDR. Skills for this position include EU MDD/MDR experience along with experience with Class II CE Mark Devices. Pluses for this position include Class III EU Medical Device and Project Management experience. The client is looking for a consultant with 3 or more years of EU MDD experience.