As a Medical Device Program Management Leader, I specialize in overseeing and executing complex, high-impact projects that drive revenue growth, cost reduction, and operational efficiency within the medical device industry. My expertise spans the entire product lifecycle, including planning, scheduling, organizing, and tracking the deployment of software and hardware solutions in live production environments across EMEA, USA, Asia-Pacific, Latin America, and China.With in-depth experience working on FDA Class III and CE Mark regulated products, I ensure strict adherence to regulatory standards while delivering innovative solutions that meet market needs. I lead cross-functional teams across development, sales, regulatory affairs, operations, implementation, and management, enabling successful commercialization and lifecycle management of medical devices.I act as a key strategic partner, aligning business goals with cutting-edge technology solutions to improve processes, enhance competitive advantage, and drive bottom-line results. My role involves managing multimillion-dollar programs, guiding teams through the intricacies of regulatory compliance, quality assurance, and market adoption, all while ensuring timely delivery of high-quality products in a global marketplace.
Listed skills include Leadership, .Net, Requirements Analysis, Sdlc, and 39 others.