Job Description
Expected Travel : Up to 25% Requisition ID : 13265 About Teleflex Incorporated As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare. Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose. At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com . 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, Ringer™ Perfusion Balloon Catheter, AC3 Optimus™ and AC3 Range™ Intra-Aortic Balloon Pumps and the OnControl™ Powered Bone Access System. Teleflex’s product portfolio now also includes Passeo™-18 Lux™ Peripheral Drug-Coated Balloon Catheter, Pantera™ Lux™ Drug-Coated Balloon Catheter, Orsiro™ Mission™ Drug-Eluting Stent, the PK Papyrus™ Covered Coronary Stent, and more. 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 This position is responsible for the project management of new product development and other initiatives. The PM is accountable for project planning and execution. They will guide core teams through project execution process in order to meet strategic objectives. The PM ensures consistent and compliant practices throughout all phases of the project life cycle and across functional teams. The PM will use influence, leadership and professional project management concepts and frameworks in accordance with company objectives and tools to inspire teams to create compelling new products. Principal Responsibilities Responsible for planning and managing global product development initiatives for the Interventional business unit. Effectively lead and drive project teams in a collaborative environment, completing project deliverables per committed timelines and scope. Monitor project budgets, directing the efficient use of resources to effectively complete projects. Lead project-related activities of project team members, providing guidance on conformance to established design control procedures. Lead, coordinate and facilitate weekly meetings, action items, and follow-up with subject matter experts on expected deliverables Prepare project summary reports, develop project plans, identifies risk and communicates mitigation activities. Prepare and deliver project status presentations to Management regularly Partner with Marketing in business gating process for projects under their responsibility Lead and/or participate in all phases of development starting with concept through post market surveillance Negotiate and resolve conflicts and drive decisions among team / functional members to accomplish project and business goals. Define project resource requirements and negotiate with functional managers to obtain resources necessary to support assigned programs. Cultivate a high performing work team culture among project core teams. Adhere to all regulatory agency standards, company quality standards and corporate policies. Must be able to travel domestically and internationally as business needs demand. Education / Experience Requirements BS in technical discipline (i.e. engineering, bio-science), advanced degree preferred 5 years of demonstrated experience in project management or project engineering working in a technical discipline, medical device and/or engineering preferred. Minimum 2 years project experience in the medical device and/or FDA regulated industry PMP