As the Associate Manager, Product Quality Clinician in the Transcatheter Mitral & Tricuspid Therapies (TMTT) division you will be a member of Complaint Handling and Post Market Surveillance/Risk Management team to provide clinical expert knowledge and clinical guidance to Quality Engineering and other cross functional teams to understand the nature of complaints and possible health risks. In this role you will ensure appropriate investigation of complaints and adverse events in order to escalate potential manufacturing, design, labeling and training issues. You will also help develop and maintain standard practices and procedures in analyzing data, interpreting and drawing conclusions, with the objective of gathering key information and communicating to cross functional teams who will utilize the information for improvement of product and procedural outcomes.
Key responsibilities include:
Education, Experience and Skills: