THE ROLE:* Assess new and existing raw materials, component, and assembly suppliers for technical and manufacturing capabilities.* Drive process/product improvements (design for manufacture/design for assembly) related to sub-assembly or component usage or design.* Develop strategies to characterize and validate new and improved manufacturing processes and components on external supplier manufacturing line and pilot lines.* Collaborate with suppliers and incoming inspection laboratories to develop, validate, and ensure appropriate inspection methods and controls are in place for components and finished devices.* Identify project risks and develop mitigation strategies to ensure supply, quality and timelines are met.* Monitor supplier performance and provide technical support to resolve issues.REQUIREMENTS:* Degree in Mechanical or Biomedical Engineering or equivalent.* At least 5-7 years of medical device medical process/device design and development experience in a regulated environment.* Experience in managing technical relationships with external suppliers and OEM is preferred.