Timothy Rice

Timothy Rice is a seasoned professional in regulatory affairs with extensive experience in the medical device industry. Currently serving as the Regulatory Affairs Program Lead at ZOLL Medical Corporation since September 2024, Timothy previously held roles at Getinge as a Regulatory Affairs Specialist and Complaint Analyst II from September 2018 to June 2024. Prior to Getinge, Timothy worked at Stryker as a Sr. Regulatory Compliance Specialist, focusing on the evaluation and submission of MDR content, and held a position as a Quality Engineer at Siemens, where responsibilities included safety evaluations and MDR submission. Timothy began the career at Pentax Medical as a Complaints Specialist responsible for record evaluation and data management. Timothy holds a Bachelor of Science (BS) degree in Global Business and a BS in Business Management from William Paterson University of New Jersey, completed in January 2009.