Principal Electrical Engineer (Hybrid - Acton, MA)
About The Position
This is a very senior-level Electrical Design Engineer role serving as a technical leader within Insulet’s R&D organization. The position is responsible for guiding the design, development, and sustainment of complex, low-power RF-controlled wearable medical devices used in infusion pump systems. In addition to hands-on design responsibilities, this individual will provide technical leadership and mentorship to engineering team members, driving best practices in circuit design, system integration, and verification. The Principal Electrical Engineer will provide senior technical leadership for the design, development, sustaining, and lifecycle management of low-power, battery-operated medical device electronics, including Bluetooth-connected wearable products. This role requires deep expertise in analog, digital, mixed-signal, power management, PCB/PCBA design, BLE connectivity, and EMI/EMC/ESD compliance. The engineer will lead complex technical efforts from early concept through post-production support, collaborate closely with cross-functional teams and external partners, mentor junior engineers, and ensure designs meet medical device quality and regulatory requirements.
Requirements
- Minimum of a Bachelor Degree in Electrical Engineering or similar discipline and minimum of 10+ years’ experience in electrical engineering related fields.
- Proficiency in analog, digital, and mixed-signal circuit design and analysis
- Demonstrated experience leading complex electronic product development efforts from concept through commercialization for medical device or wearable device markets.
- Strong expertise in all aspects of wireless communications, particularly Bluetooth Low Energy (BLE) connectivity.
- Solid expertise in all aspects of PCB/PCBA design, schematic review, layout, and BOM management.
- Strong background in embedded electronics design (ARM/RISCV processors).
- Demonstrated expertise in device-level EMI/EMC/ESD design, test, and analysis.
- Experience working with external compliance labs and managing external service providers.
- Hands-on experience with lab equipment: oscilloscopes, logic analyzers, signal generators, VNA, spectrum analyzer, etc.
- Proficiency in Microsoft Office (Word, Excel, PowerPoint)
- Experience with engineering tools: Cadence OrCAD, Altium CAD, PCB Editor, MATLAB, Minitab
- Strong verbal and written communication skills
- Ability to present projects or new ideas to senior management.
- Strong problem solving and root-cause analysis skills
Nice To Haves
- Master’s degree in EE or similar discipline
- Medical wearable device design experience
- Programming experience in C/C++, Python, and MATLAB is highly desirable
- Working knowledge of RF/EMI simulation tools utilized in the electrical engineering field, including HFSS, Cadence, and ADS.
- Data analytics skills.
- Experience deploying and using AI tools.
Responsibilities
- Lead product sustaining and life-cycle engineering effort for current production products.
- Take ownership of the electronics part of the product from early design stage all the way to post-production support.
- Serve as a technical lead, mentor and a role model for junior engineers.
- Act as a technical authority for electrical engineering disciplines including analog, digital, mixed-signal, power management, and wireless communications.
- Propose and champion new ideas for product improvements.
- Design new and re-design existing low-power battery operating devices, including Bluetooth-connected wearable devices or similar wireless-enabled medical technology.
- Architect, review, and approve Block Diagrams, Schematics, PCB Layout, and Bills of Material (BOM).
- Define and execute EMI/EMC/ESD requirements and compliance test plans for the product, including defining and reviewing compliance pre-screening and test plans.
- Design and execute BLE connectivity on-body characterization plan.
- Lead root cause analysis for design and manufacturing issues at the PCB/PCBA and system level.
- Ensure design and documentation comply with medical device quality system guidelines, including FDA design control guidelines, ISO 13485, 21 CFR 820, and IEC 62304.
- Ensure smooth design transfer from R&D to Manufacturing and post-release support.
Benefits
- Medical, dental, and vision insurance
- 401(k) with company match
- Paid time off (PTO)
- Additional employee wellness programs
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What This Job Offers
Job Type
Full-time
Career Level
Senior
