Lead medical device quality engineering at Verathon in Burnaby, applying risk management and design controls across product development initiatives.

As a Design Quality Engineer II, you will support recent product development and sustaining engineering throughout the product lifecycle. You will collaborate with product development engineering and core teams on quality deliverables. Your work includes validation, compliance testing, failure analysis, and cybersecurity assessments.

Key Responsibilities:

- Develop quality plans and risk management strategies
- Review and approve design verification and validation protocols
- Execute design control and risk management deliverables
- Maintain uFMEA and dFMEA analyses with engineering teams
- Lead failure investigations and CAPA initiatives

Requirements:

- Bachelor’s degree in an engineering discipline
- P.Eng or Engineer-in-Training eligibility
- Minimum three years of quality engineering experience
- Medical device or related industry experience
- Knowledge of ISO, IEC, and FDA standards

Apply quality engineering, statistical analysis, and cross-functional communication to advance compliant medical device development at Verathon.

📌 Medical Device Quality Engineer (Burnaby)
🏢 Verathon
📍 Burnaby