Electronics Engineer, Medical Devices - Reg & V&V Focus
Qidni Labs
Kitchener
On-site
CAD 80,000 - 100,000
Full time
14 days+
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Job summary
A leading medical device company in Kitchener, Canada is seeking a talented Electronics Engineer to design and develop electronic systems for medical devices. The ideal candidate will have strong experience in analog, digital, and embedded circuit design, an understanding of regulatory requirements, and the ability to work through full product development lifecycles from concept to production. This role involves collaboration with cross-functional teams and compliance with necessary standards.
Qualifications
Bachelor’s degree in Electrical Engineering or related field (Master’s preferred).
4+ years of experience in electronics design.
Strong experience in analog and digital circuit design, embedded systems, and microcontrollers.
Experience with oscilloscopes, logic analyzers, and lab instrumentation.
Understanding of power electronics and low-noise design.
Strong documentation and communication skills.
Responsibilities
Design and develop analog and digital circuits for medical devices.
Perform schematic capture, PCB layout, and prototype bring-up.
Conduct circuit simulations, tolerance analysis, and design verification testing.
Support EMI/EMC design and pre-compliance testing.
Develop and execute verification and validation (V&V) test protocols.
Contribute to design reviews and technical documentation.
Ensure designs comply with applicable standards.
Support regulatory submissions and audits as required.
Collaborate with manufacturing teams for DFM/DFT optimization.
Support product transfer to manufacturing and production troubleshooting.
Investigate field issues and implement corrective actions.
Job description
A leading medical device company in Kitchener, Canada is seeking a talented Electronics Engineer to design and develop electronic systems for medical devices. The ideal candidate will have strong experience in analog, digital, and embedded circuit design, an understanding of regulatory requirements, and the ability to work through full product development lifecycles from concept to production. This role involves collaboration with cross-functional teams and compliance with necessary standards.