Global Adverse Event Reporting Specialist II (Temporary)
Terumo Cardiovascular Group
Terumo Cardiovascular Group in Elkton, MD, seeks a qualified Adverse Event Reporting Spec II for a temporary position. This role entails assisting with Medical Device Reporting to health authorities and involves tasks such as reviewing complaints, maintaining MDR logs, and ensuring compliance with regulations. The ideal candidate has a Bachelor’s Degree in health or related field and at least 3 years of quality assurance experience. Competitive salary and comprehensive benefits package including health insurance and a 401(k) plan offered. #J-18808-Ljbffr
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