Description
The Associate Quality Engineer maintains quality and control of medical device manufacturing processes and post-market performance. The role leads root-cause investigations, develops risk-based decisions, resolves customer complaints and manufacturing nonconformities, analyzes product performance, troubleshoots returned devices, documents technical findings, and supports cross-functional quality projects. It requires 0–2 years of experience in a medical device or pharmaceutical regulated industry, a bachelor’s degree with engineering or physical science coursework, and proficiency in project management, data analysis, root cause analysis, communication, and risk determination.
