Adverse Event Reporting & Global Vigilance Specialist

The Adverse Event Reporting & Global Vigilance Specialist provides quality and regulatory support for adverse event reporting, medical device reporting, and global vigilance activities at Terumo BCT. The role involves reviewing complaints, evaluating reportability, preparing regulatory submissions, and maintaining accurate, audit-ready records in compliance with global standards. This position supports cross-functional coordination, timeline tracking, and continuous improvement of post-market quality processes.