Description
The Quality Engineer will lead cross-department collaboration and serve as a subject matter expert on quality, design controls, risk, and regulatory compliance in medical device development. The role is primarily focused on new product development, with responsibilities including design control, statistical analysis, testing and inspection procedures, risk-based sampling, software validation, FMEA workshops, quality management system compliance, continuous improvement, and CAPA support. The position is onsite in Salt Lake City, Utah, requires a bachelor’s degree in engineering or a related field, and prefers 7–9 years of experience.
