Senior Principal Electrical Engineer

MiniMed • Los Angeles, CA

1d

About The Position

MiniMed 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.

Requirements

• Requires a Bachelor's degree and minimum of 10 years of relevant experience OR Master's degree with a minimum of 8 years relevant experience OR PhD with 6 years relevant experience.

Nice To Haves

• 5+ years of hands-on experience with electrochemical biosensing systems
• Deep understanding of electrochemical principles (cyclic voltammetry, impedance spectroscopy, potentiometry)
• Experience with biosensor fabrication techniques and electrode materials
• Knowledge of biocompatibility requirements and sensor packaging for biological environments
• Experience with wireless communication protocols (Bluetooth, NFC) for medical devices
• Proficiency in circuit simulation tools (SPICE, Cadence) and PCB design (Altium )
• Deep knowledge of PCBA design and manufacturing processes
• Previous experience with continuous glucose monitoring or other implantable sensors
• Experience with ISO 14971 risk management processes
• Publication record in peer-reviewed journals related to biosensing

Responsibilities

• 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.
• 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
• 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
• 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.

Benefits

• MiniMed offers a competitive salary and flexible benefits package
• We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every stage of your career and life.
• This position is eligible for a short-term incentive called the Short Term Incentive (STI).
• Regular employees working 20 or more hours per week are eligible for a robust benefits package, including health, dental, and vision insurance, as well as access to a Health Savings Account, Healthcare Flexible Spending Account, life insurance, long-term disability leave, and a dependent daycare spending account.
• In addition, all regular employees enjoy incentive plans, a 401(k) plan with company match, short-term disability coverage, paid time off and holidays, participation in our Employee Stock Purchase Plan, and access to our Employee Assistance Program.
• Eligible employees may also benefit from our Non-qualified Retirement Plan Supplement and Capital Accumulation Plan, subject to IRS minimum earnings requirements.

What This Job Offers

• Job Type: Full-time
• Career Level: Senior