.**About Teleflex Incorporated****Interventional -** The Interventional business unit at Teleflex offers innovative medical devices that are used to diagnose and treat coronary and peripheral vascular diseases. We place a strategic emphasis on complex coronary and peripheral interventions, vascular access, bone access, specialty biologic treatments and cardiac assist. Our current Interventional products include a broad range of clinically relevant solutions, such as our GuideLiner® and Turnpike® Catheters, AC3 Optimus Intra-Aortic Balloon Pump and OnControl® Powered Bone Access System. With a strong R&D footprint and pipeline, our fast-growing Interventional business unit is poised to continue the development of new technologies to serve critically ill patients for years to come. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients' lives.**Position Summary**:**Principal Responsibilities**:- Provide engineering support to design and/or process alterations to existing products- Manage engineering activity required to support products through the commercialized life cycle- Coordinate Design Change and Process Change activities- Assess proposed Design and Process Changes for the impact to the organization; create evidence based project proposals- Develop design inputs and design outputs for changes to existing product- Develop new test methods and/or alter existing test methods- Provide R&D support for verification, qualification, and validation studies on existing products- Support risk management activities and risk management reviews on existing products- Provide R&D support for non-conformance investigations regarding component failures, finished goods failures, and product returns.- Provide R&D support for customer complaints, including product/record investigation, health risk assessments, identification of CAPA's, and report generation.- Support regulatory approvals and responses to regulatory questions for existing products.- Lead commercialized product change project teams and maintain design history files- Ensure design change and process change activities, processes and practices are in compliance with internal quality system requirements.- Maintain and supplement design history files that are thorough and accurate for existing product- Interview, select, train and evaluate performance of new hires- Mentor and train Sustaining Engineers- Ensure company policies and procedures are followed taking timely corrective action with the help of HR when necessary**Education / Experience Requirements**:- Bachelor's degree in a relevant field.- Six years of relevant experience required.**Specialized Skills / Other Requirements**:- Must possess knowledge, understanding and skills in: product designs/concepts, catheter materials, project management, documentation, and a working knowledge of quality systems and medical device regulations