Description
The Quality Engineer will lead risk assessments, test methods, component and design validation, process validation, product investigations, and manufacturing control plans for a medical device product line. The role coordinates product development activities, supports regulatory submissions and supplier audits, leads cross-functional teams, and requires a BS in Engineering plus at least two years of engineering or quality engineering experience in a medical device, pharmaceutical, or equivalent industry. The position is based in Tempe, Arizona, with approximately 25% travel.
