Global Adverse Event & MDR Reporting Specialist II

A leading medical device company in Elkton, Maryland seeks a Regulatory Affairs Specialist to assist with Medical Device Reporting (MDR) and compliance with health authorities. The role includes reviewing complaints, coordinating information requests, and maintaining regulatory logs. Candidates should possess a Bachelor's degree in a relevant field and have three years of experience. Competitive salary and comprehensive benefits package available, including bonus opportunities and health insurance. #J-18808-Ljbffr