Senior Regulatory Affairs Lead – Medical Devices (FDA/EU MDR)

A leading medical technology company is seeking a Principal Regulatory Specialist with extensive experience in regulatory affairs. The role involves managing regulatory submissions and ensuring compliance with U.S. and EU requirements. Candidates should have at least a Bachelor's degree and 7+ years of experience in the field. The position offers a hybrid work model based in Arden Hills, MN, with competitive compensation ranging from $99,100 to $188,300, commensurate with experience. #J-18808-Ljbffr