Role Summary
As part of the EE team, this engineer will participate in all phases of the development of medical devices from early concept through clinical use. Â Develop and prototype electronic circuit designs supporting active medical implant technology. Â Apply engineering and scientific principles to the evaluation and solution of technical problems. Â Create and execute both formal and informal test plans and procedures and produce test reports. Â Work will involve all phases of product development, including circuit design and simulation, component selection and sourcing, PCB layout, circuit and system test, and test system and procedure development. Â Work closely with other departments to ensure timely delivery of a quality product. Â May include device manufacturing support failure analysis to root cause, process improvements, test system support, technical support to partner company, etc. Â The position is expected to increase in self-directed work with time and experience. Â
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Essential Responsibilities
- Support the engineering design, analysis, and verification for electrical medical devices.
- Create and maintain engineering documentation including requirements, schematics, assembly drawings, and BOMs.
- Lead and participate in design reviews—providing and receiving critical design feedback.
- Troubleshoot software-controlled analog and digital SMT circuit boards.
- Perform component-level testing and analysis using standard lab equipment.
- Collaborate with cross-functional teams to refine specifications, optimize processes, and improve yield and cost.
- Ensure compliance with internal Quality System requirements across all engineering documentation.
- Design and development of efficient test procedures in accordance with defined specifications.
- Design, conduct and report experiments, to verify and validate the product input specifications.
- Support product design verification at external labs.
- Mentor and support technicians and assemblers in execution of technical tasks.
Skills and Experience
Required qualifications:
- Bachelor’s degree or higher in electrical engineering or a related field from an accredited institution.
- Minimum of 2 years' experience in electrical engineering, particularly in product development environments.
- Experience designing, simulating, and analyzing analog and digital circuits – min. 2 years.
- Ability to evaluate and select components based on defined system requirements.
- Experience using test equipment such as multimeters, oscilloscopes, signal generators, and network analyzers, as well as manual tools such as soldering irons and crimpers.
- Proficiency with electronic design tools for schematic capture and PCB layout review.
- Ability to travel 10% of the time.
Preferred qualifications:
- Experience using Altium Designer for schematic development, PCB layout, and fabrication documentation.
- Experience using LTSpice as part of the design and troubleshooting process.
- Previous patent applications a plus.
- Background in a regulated industry, preferably with Class II or III medical devices.
- Familiarity with ISO 14708, EN 60601, and FDA Quality System Regulations.
- Exposure to firmware development or embedded systems design.
- Experience in systems engineering and requirements management a plus.
- Strong verbal and written communication skills with the ability to clearly convey technical concepts.
- Ability to manage tasks independently while collaborating across multidisciplinary teams.
- Ability to work cross-functionally across engineering, quality, regulatory, and manufacturing.
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