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