Nurse Specialist Job in Tempe, Arizona US
Participation in the decision making, development, and/or review process related to post-market adverse event reporting in the U.S. (Medical Device Reporting -MDR), Europe (Medical Device Vigilance -MDV), and other adverse event reporting requirements for International regulatory bodies around the world.Participant in the decision making, development, and/or review process related to product complaints.Interfaces with worldwide regulatory bodies related to inquiries associated with customer complaints and adverse events.Responsible for reviewing patient medical records involving customer complaints.Assessment Read more […]