Electrical Engineer II — Implantable Medical Devices

Senseonics, Incorporated; Maple Grove (MN); On-site; USD 85,000 - 120,000; Full time

Job summary

Senseonics, Incorporated is seeking an Electrical Engineer II to join our R&D team, designing electrical and electronic systems for next-generation implantable CGM devices. You will take increasing ownership of circuit design, testing, and design controls within a regulated medical device environment.

You will collaborate with mechanical, firmware, systems, and quality engineers through the product development lifecycle—from concept to verification and design transfer—and contribute to risk

Qualifications

• Bachelor's degree in Electrical Engineering required.
• 2–5 years in electrical/electronic design, preferably medical devices.
• Experience with schematic capture and PCB layout tools.
• Strong problem-solving and meticulous attention to detail.
• Excellent written and verbal communication.

Responsibilities

• Design, simulate, and prototype analog and digital circuits for implantable and non-implantable devices.
• Develop schematics, PCB layouts, and BOMs with mechanical and vendor teams.
• Select components considering performance, cost, and regulatory requirements.
• Build, test, and debug prototypes; conduct bench-level characterization.
• Support V&V activities; document test results and protocols.
• Contribute to risk management and regulatory documentation.
• Collaborate with firmware, mechanical, systems, and quality teams.
• Participate in design reviews and maintain design history files.

Skills

Circuit design fundamentals

Analog and digital design

Schematic capture

PCB design

Analytical problem-solving

Technical communication

Education

Bachelor's degree in Electrical Engineering

Tools

Altium Designer

OrCAD

Eagle

Job description

Senseonics, Incorporated is seeking an Electrical Engineer II to join our R&D team, designing electrical and electronic systems for next-generation implantable CGM devices. You will take increasing ownership of circuit design, testing, and design controls within a regulated medical device environment.

You will collaborate with mechanical, firmware, systems, and quality engineers through the product development lifecycle—from concept to verification and design transfer—and contribute to risk