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Principal or Senior Electrical Engineer

Kaav Inc
locationBurlington, MA, USA
PublishedPublished: 6/14/2022
Manufacturing
Full Time

Job Description

Job Description

Job Title: Principal / Senior Electrical Engineer (Medical Devices)
Location: Burlington, MA – Hybrid (3 days onsite, no remote) - (Only USC and GC)
Domain: Medical Devices – Complex Electro-Mechanical Systems
Visa: US Citizens / Green Card holders only

Compensation:

Job Overview

We are seeking a highly skilled Principal or Senior Electrical Engineer with 8–10+ years of experience in medical device design and development. This role is hands-on and will focus on analog/digital circuit design, PCB layout, and embedded programming, working across all phases of product development—from concept through production.

The ideal candidate has a strong background in medical device standards (IEC 60601, ISO 13485, FDA) and thrives in a cross-functional environment delivering innovative, safe, and compliant medical technologies.

Key Responsibilities

  • Design and develop analog and digital circuits, including low-noise analog, sensor interfaces, and power management systems.

  • Perform PCB layout and ensure compliance with EMC/EMI requirements.

  • Write, debug, and maintain embedded C code for microcontrollers.

  • Collaborate with cross-functional teams (mechanical, systems, software) for system integration.

  • Ensure designs meet medical device regulations and quality standards (IEC 60601, ISO 13485, FDA).

  • Support verification, validation, and transfer to manufacturing activities.

  • Provide documentation, troubleshooting, and technical leadership in design reviews.

Qualifications

  • B.S. in Electrical Engineering (M.S. preferred).

  • 8–10+ years of experience in medical device electrical design.

  • Proven expertise in:

    • Analog/digital circuit design

    • PCB design tools and layout

    • Embedded C programming

  • Strong knowledge of low-noise analog, sensor interfaces, power management, and EMC/EMI compliance.

  • Hands-on troubleshooting and root-cause analysis skills.

  • Familiarity with medical device regulatory frameworks (IEC 60601, ISO 13485, FDA).

  • Excellent communication, documentation, and cross-team collaboration abilities.

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