Youâll partner with product development teams to deliver design quality for complex electromechanical medical devices and consumables. This role focuses on translating user needs into design requirements, guiding risk and test strategies, and ensuring design documentation and verification align with global medical device standards.
Requirements
- Bachelorâs degree in Science, Engineering, or a related discipline
- Minimum 6 years of experience in medical device product development and/or design quality engineering
- Experience working within highly regulated industries with formal quality systems and design documentation practices (e.g., ISO 13485 or comparable industry standards)
- Experience with design controls, risk management, and verification/validation planning for electroâmechanical products
Benefits
- 401k Matching
- Retirement Plan
- Generous Paid Time Off
- Health insurance
- Other benefits (not specified)