Staff Software Quality Engineer, Post Market Integration

What you’d do

Lead quality engineering work including complaint investigations, root cause analysis, CAPA, and field actions for medical devices. Partner with R&D, operations, and commercial teams on risk management and continuous improvement. Full time. Found on the employer's careers page on Oct 18, 2026. Apply through the link.

You’ll need

• Medical device industry experience
• Knowledge of ISO 13485, GDP, and GMP
• U.S. and international medical device regulations
• Root cause analysis and CAPA experience
• Working knowledge of computer hardware