1)Performed safety assessments of medical devices and identify potential safety concerns2)Conducted risk assessments and implement risk management strategies to mitigate potential safety concernsCollaborated with cross-functional teams, including Regulatory Affairs, Clinical Affairs, Quality Assurance, and Engineering, to ensure that medical devices meet regulatory requirements and are safe for use by patients and healthcare professionals3)Supported the development and implementation of post-market surveillance plans and perform trend analyses of adverse events related to medical devices4)Assisted in the preparation of reports for regulatory agencies related to medical device safety5)Stayed up-to-date with the latest regulatory requirements related to medical device safety and communicate changes to the team