- Terumo Medical Corporation (Elkton, MD)
- Adverse Event Reporting Spec II Date: Nov 14, 2025 Req ID: 5335 Location: Elkton, MD, US Company: Terumo Medical Corporation Department: Post Market ... US and global health authorities (GHA) such as FDA, HC, MHRA, etc. The Adverse Event Reporting Team is responsible with implementation of best practices to… more