The Director will operate at the intersection of clinical need, customer workflow, technology, and business strategy , partnering closely with R&D, engineering, Clinical Affairs, Quality & Regulatory, Operations, Supply Chain, and Commercial teams to guide the development of a complex medical device from early concept through product realization. "It is Siemens Healthineers' policy to comply fully and completely with all United States export control laws and regulations, including those implemented by the Department of Commerce through the Export Administration Regulations (EAR), by the Department of State through the International Traffic in Arms Regulations (ITAR), and by the Treasury Department through the Office of Foreign Assets Control (OFAC) sanctions regulations.".