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Summer Embedded C Programming Jobs in Boston, MA

Company Description Sriramprasath Email : sriram at krgtech dot com 661 558 0000 * 505 1)Minimum 5 year experience in Embedded C development 2) Working Knowledge on System Power Optimization 3) ...

Software Engineer ( Embedded)

Essex, MA · On-site

$138K - $182K/yr

Company Description Thanks & Regards Rajesh KRG Technologies, Inc., 661 558 0000 Ext :514 1)Experience in Embedded C development 2) Working Knowledge on System Power Optimization 3) Awareness/Working ...

Senior Embedded Engineer

Boston, MA · Hybrid

$134K - $176K/yr

Advance-level proficiency in embedded C and embedded C++ targeting the ARM Cortex-M family of ... systems engineers. * Experience in Android Open Source Project (AOSP) or embedded Linux is a ...

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Summer Embedded C Programming information

See Boston, MA salary details

$40.2K

$140.2K

$433.5K

How much do summer embedded c programming jobs pay per year?

As of Aug 11, 2026, the average yearly pay for summer embedded c programming in Boston, MA is $140,247.00, according to ZipRecruiter salary data. Most workers in this role earn between $93,400.00 and $144,500.00 per year, depending on experience, location, and employer.

What is the difference between Summer Embedded C Programming vs Summer Firmware Developer?

AspectSummer Embedded C ProgrammingSummer Firmware Developer
Required SkillsEmbedded C, microcontroller programming, hardware interfacingEmbedded C, firmware design, hardware-software integration
Work EnvironmentHardware labs, embedded systems projectsEmbedded systems development, hardware testing
Industry UsageConsumer electronics, automotive, IoT devicesConsumer electronics, industrial automation

Both roles focus on embedded systems programming using C, often in similar industries. Summer Embedded C Programming emphasizes microcontroller coding and hardware interfacing, while Summer Firmware Developer may involve more firmware design and integration tasks. They share skills and work environments, making them closely related but with slight differences in focus.

Principal or Senior Electrical Engineer

Kaav Inc

Burlington, MA • On-site

$151K - $185K/yr

Contractor

Re-posted 27 days ago


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.