MDR & Adverse Event Reporting Specialist II
Terumo Medical Corporation
Terumo Medical Corporation in Elkton, MD is seeking an Adverse Event Reporting Spec II to support the Post Market Surveillance group with Medical Device Reporting to US and global health authorities. The role focuses on ensuring timely, accurate submissions and assisting with audits, regulatory requests, and quality system improvements. The ideal candidate has a health/regulatory background and experience in a regulated industry. #J-18808-Ljbffr Terumo Medical Corporation
Vacancy posted 2 days ago
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