We anticipate the application window for this opening will close on - 15 Jan 2026

 

At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

A Day in the Life

Medtronic Diabetes is seeking a highly experienced Senior Principal Electrical Engineer with specialized expertise in electrochemical biosensing to lead the development of next-generation medical devices. This role requires deep technical knowledge in biosensor design, electrochemical systems, and medical device regulations to drive innovation in diagnostic and therapeutic applications.

As a Senior Principal Electrical Engineer, you will play a critical leadership role in the design, development, and optimization of cutting-edge electrochemical glucose sensor technology for diabetes management. You will provide technical expertise, drive innovation, and guide cross-functional teams to deliver safe, effective, and reliable medical devices that improve patient outcomes. Candidates must be willing to work in a fast-paced, multi-tasking, team environment.

Join a passionate team dedicated to transforming diabetes care through innovative sensor technology. You’ll have the opportunity to make a meaningful impact on patients’ lives and work with some of the brightest minds in the medical device industry.


This position is an exciting opportunity to work with Medtronic's Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility. As a separate entity, we anticipate leveraging

Responsibilities may include the following and other duties may be assigned. ​

Technical Leadership:

• Lead the electrical design and development of advanced electrochemical glucose sensor systems, including circuitry, embedded systems, and signal processing algorithms.

• Define and execute verification and validation strategies for sensor electronics, ensuring compliance with relevant medical device standards (ISO 13485, IEC 60601, etc.).

• Drive innovation through the evaluation and adoption of new materials, sensor architectures, and low-power electronics.

• Oversee design documentation, risk analysis, and failure mode analysis (FMEA) for sensor-related components.

• Interface with external partners, suppliers, and research organizations to advance sensor technology.

• Present technical findings and project updates to executive leadership and cross-functional stakeholders.

 Design & Development:

• Architect electrical systems for continuous glucose monitors or other diagnostic platforms

• Develop signal conditioning circuits, analog front ends, and data acquisition systems for biosensor applications

• Design low-noise, high-precision potentiostat circuits and amperometric measurement systems

• Develop algorithms for signal processing, noise reduction, and biomarker detection

• Create electrical interfaces between biosensors and embedded systems

• Optimize sensor performance parameters including sensitivity, selectivity, and stability

• Drive innovation in sensor miniaturization, power optimization, and wireless connectivity

Technical Oversight:

• Collaborate with chemistry, mechanical, software, systems, and manufacturing teams to integrate sensor technology into commercial diabetes devices.

• Mentor and guide junior engineers and project teams in design best practices, troubleshooting, and root cause analysis.

• Review and approve electrical designs, test protocols, and validation procedures

• Lead design reviews and risk analysis activities

Regulatory & Quality:

• Ensure designs comply with FDA regulations (21 CFR Part 820), IEC 60601, and ISO 13485

• Support regulatory submissions including 510(k) and PMA applications

• Implement design controls and verification/validation protocols per medical device standards

• Partner with regulatory and quality teams to support submissions, audits, and compliance activities.

Required Knowledge and Experience: