Description
We are seeking a Senior Electrical Engineer on behalf of our client, a leading innovator in advanced medical device technology. This role is a key position within the R&D team and offers the opportunity to contribute to the full lifecycle of cutting-edge electromechanical systems — from concept and design to manufacturing and post-launch support.
If you’re passionate about designing technology that truly makes a difference in people’s lives, this is an opportunity to bring your expertise to a collaborative, mission-driven environment.
Key Responsibilities
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Lead all electrical engineering aspects of medical device design, including schematic capture, PCB layout, requirements management, verification test design, and manufacturing design transfer.
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Ensure compliance with medical device design control regulations and internal quality procedures.
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Design and develop electronics for electromechanical assemblies, wired and wireless systems, and ensure compliance with IEC 60601-1 and related safety/EMC standards.
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Collaborate cross-functionally with mechanical, software, quality, and manufacturing teams, as well as clinicians, regulatory, and marketing partners.
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Coordinate with external test labs to support global compliance and certification efforts.
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Drive continuous improvement through cost reduction, process enhancement, and design optimization initiatives.
Qualifications
Minimum Requirements
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Bachelor’s degree in Electrical Engineering or related discipline.
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Proven experience in electrical design within a regulated industry (medical device experience strongly preferred).
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Hands-on technical expertise in design for manufacturing and design for quality.
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Strong analytical and problem-solving skills, including familiarity with verification, validation, and DOE methodologies.
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Ability to manage multiple concurrent projects and thrive in a collaborative, cross-functional environment.
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Excellent communication and documentation skills.
Preferred Qualifications
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Proficiency with ECAD tools such as Altium Designer.
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Working knowledge of FDA QSR (21 CFR Part 820), EU MDR 2017/745, ISO 13485, ISO 14971, and IEC 60601-1.
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Experience with injection molding and manufacturing processes.
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Proficiency with SolidWorks or similar 3D CAD software.