Medical Device MDR & Adverse Event Specialist
Terumo Cardiovascular Group
Terumo Medical Corporation in Elkton, MD seeks a QA professional to support Post Market Surveillance and Vigilance through Medical Device Reporting (MDR) for US and global health authorities. You will work with Complaints, Engineering, and Quality to ensure accurate, timely submissions and maintain regulatory documentation. Responsibilities include audits, process improvements, and cross-training with the team to sustain compliance across Terumo facilities. #J-18808-Ljbffr Terumo Cardiovascular Group
Vacancy posted 3 days ago
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