PE Global is recruiting for an Electronic Engineer for our medical device client in Galway. This is an initial 12-month contract, onsite role.
Responsibilities will include but are not limited to:
· Decompose and develop electrical-based product requirements from system-based requirements
· Integrate electrical design into risk process, including DFMEA development.
· Conduct electrical design, design outputs, and characterization result reviews.
· Ensure integration between electrical hardware and firmware.
· Apply best practice electrical design techniques in areas such as PCBA design, FPGA, motor controls, custom battery design to ensure design partners adequately meet product and program needs.
· Work closely with other design teams (Electrical, Systems, Firmware and Mechanical) to root cause design issues, create test suites, characterize, and ultimately verify electrical product designs.
· Characterize and analyze product performance using DFSS techniques.
· Validate test environments comprising custom equipment, software, and test methods.
· Perform and document verification of electrical product requirements.
· Interface with certified test houses to verify/certify to global regulatory standards including ISO 14971, IEC 60601, etc.
· Support of design transfer to operations and release product engineering organizations.
· Serve as the electronics expert and primary point of contact for cross functional partners.
· Work under minimal supervision.
· Ensure understanding of all quality policy/system items that are personally applicable. Follow all work/quality procedures to ensure quality system compliance and high-quality work.
· Ability to work with others internationally and travel globally.
Must Have: Minimum Requirements
· 4+ years of Electrical Product Development experience in medical devices.
· Design and test devices in a global regulated environment including 60601 EMI/EMC, ISO 14971 and 60601 safety.
· Electrical engineering skills to design, develop, and debug analog and digital circuitry, custom batteries, motor/motion control for electromechanical medical device product development.
· Ensure understanding of all quality policy/system items that are personally applicable.
· Follow all work/quality procedures to ensure quality system compliance and high-quality work.
· Bachelor's degree in a technical discipline
Nice to Have
· BS or MS in Electrical or Computer Engineering
· Experience with verification and validation medical devices
· Experience developing automated test benches
· Experience validating test scripts, methods and systems
· Experience in hardware firmware integrations
Interested candidates should submit an updated CV.
Please click the link below to apply, call Paul Wheatley on or alternatively send an up-to-date CV to
***Please note our client cannot assist with any visa sponsorship and candidates must have the correct visa to live and work in Ireland***