The candidate shall be experienced in effectively managing interdisciplinary projects while working in an ISO 13485/FDA regulated environment, and be responsible for key product design and development work. The candidate shall have broad experience and demonstrated creativity and effectiveness in implementing materials and fabrication processes during the development of commercial medical devices, including injection molding, machining, welding, casting, and bonding of plastics, elastomers, metals, coating and plating, and other high and low volume manufacturing techniques. Also required is experience in developing protocols, measurements and tests, and design of experiments for development of medical devices and electromechanical devices. The candidate shall have experience in the integration of electronics, software, industrial design, and design for manufacturability of medical devices. Demonstrable proficiency with SolidWorks is required (Pro/E expertise may be substituted). Experience in performing engineering analysis and modeling such as stress-strain, heat transfer, fluid flow, and machine dynamics is desired. Must have a BS/MS in Mechanical Engineering and minimum of four years experience in the medical device industry and 8-10 years experience in electro-mechanical packaging design, analysis and documentation.
