Responsibility

– Research design options and perform experiments to determine potential design feasibility

– Develop and test new manufacturing process

– Work closely with electrical and software engineers, designing with a system-wide perspective

– Interact with global and internal design and manufacturing resources to design for manufacturability, reliability, and cost-effectiveness

– Specify and manage tool development

– Create and release product requirements, design specifications and design descriptions for assigned projects, as required by applicable medical device standards and internal procedures

– Follow all policies, procedures, and standards for engineering documentation to ensure compliance with corporate document management policy

– Review product documentation for accuracy, including documentation intended for customer use

– Participate in all designing, prototyping, testing and qualification of mechanical designs for high-reliability and high-performance medical devices

– Participate in or support risk assessment, design reviews, pre-production, pilot production, testing, and regulatory submission

– Support production activities and resolve issues quickly

– Evaluate product non-conformances and recommend design modifications through advanced analytical and problem-solving techniques

– Support the development of intellectual property