Staff Design Quality Engineer

What you’d do

Provide quality and regulatory guidance on new product development teams for medical devices. Review design control documents, apply risk management, support validation and design transfer, and investigate product issues. Full-time in Waltham, MA. Found on the employer's careers page on Oct 22, 2026. Apply through the link.

You’ll need

• Certified Quality Engineer (CQE) or comparable quality certification
• Experience with Class II and/or Class III medical devices
• Knowledge of EU Medical Device Regulation and Medical Device Single Audit Program
• Experience with design control documentation and risk management
• Full-time schedule