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Medical Device Embedded System Engineer Jobs in Fall River, MA

Senior Electrical Research Engineer

Mansfield, MA · On-site

$113K - $148K/yr

... medical device safety standards Requirements development and management for embedded systems ... engineering practices, product safety and root cause analysis. Additional Information To get ...

... medical device safety standards Requirements development and management for embedded systems ... of engineering practices, product safety and Additional Information To know more about this ...

This Embedded Software Engineer role focuses on designing and developing high-quality software for ... medical device software. You will work with embedded systems, hardware platforms, and cloud ...

Embedded Firmware Engineer

Bristol, RI · On-site

$107K - $147K/yr

About Vatn Systems Vatn Systems is an innovative startup at the forefront of designing and ... Bring up new hardware: board bring-up, bootloaders, device drivers, and board support packages

Use Git-based version control systems, including GitHub Enterprise, to manage source code and ... Medical, dental & vision * Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre ...

Senior Software Engineer

Providence, RI · On-site

$113K - $162K/yr

... medical device products. You'll lead technical initiatives from concept through manufacturing ... You'll work on a diverse set of technologies, from highly efficient, low-power embedded systems ...

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Showing results 1-20

Medical Device Embedded System Engineer information

See Fall River, MA salary details

$62.7K

$137.8K

$192.7K

How much do medical device embedded system engineer jobs pay per year?

As of Aug 13, 2026, the average yearly pay for medical device embedded system engineer in Fall River, MA is $137,801.00, according to ZipRecruiter salary data. Most workers in this role earn between $111,900.00 and $164,100.00 per year, depending on experience, location, and employer.

What does a medical device embedded system engineer do?

A Medical Device Embedded System Engineer designs, develops, and maintains the embedded software and hardware used in medical devices such as pacemakers, infusion pumps, and diagnostic equipment. They ensure that the systems meet strict safety, reliability, and regulatory standards required in the healthcare industry. Their work involves programming microcontrollers, integrating sensors and communication modules, and collaborating with cross-functional teams to ensure the final product is safe, effective, and compliant with medical regulations.

How does a medical device embedded system engineer typically collaborate with cross-functional teams during product development?

As a Medical Device Embedded System Engineer, you’ll work closely with teams such as hardware engineers, software developers, quality assurance, regulatory affairs, and clinical experts. Collaboration is essential to ensure the embedded system meets safety, performance, and regulatory requirements. This often involves participating in design reviews, troubleshooting integration issues, and providing technical documentation. Effective communication and teamwork are key, as you’ll be translating clinical needs into technical solutions and ensuring compliance with medical standards.

What are the key skills and qualifications needed to thrive as a medical device embedded system engineer, and why are they important?

A Medical Device Embedded System Engineer typically needs a strong background in electrical or computer engineering, experience with embedded C/C++ programming, and a solid understanding of medical device regulations. Familiarity with microcontrollers, real-time operating systems (RTOS), and compliance standards like IEC 62304 is highly valuable, and certifications in embedded systems or medical device software can be advantageous. Strong problem-solving skills, attention to detail, and effective teamwork are essential soft skills for excelling in this position. These competencies ensure the development of safe, reliable, and regulatory-compliant medical devices that improve patient outcomes.

What is the difference between Medical Device Embedded System Engineer vs Medical Software Engineer?

AspectMedical Device Embedded System EngineerMedical Software Engineer
CredentialsBachelor's or higher in Electrical, Computer Engineering, or related; knowledge of embedded systemsBachelor's or higher in Computer Science, Software Engineering, or related; programming skills
Work EnvironmentDesigning and testing embedded hardware/software for medical devicesDeveloping medical software applications, often on PCs or servers
Industry UsageUsed in medical devices like pacemakers, imaging equipment, and monitorsUsed in healthcare software, EHR systems, and medical data analysis

The Medical Device Embedded System Engineer focuses on developing embedded hardware and firmware for medical devices, ensuring safety and compliance. In contrast, the Medical Software Engineer primarily develops software applications used in healthcare settings. Both roles require technical expertise but differ in their focus on hardware versus software development within the medical industry.

What cities near Fall River, MA are hiring for Medical Device Embedded System Engineer jobs?

Cities near Fall River, MA with the most Medical Device Embedded System Engineer job openings:

Infographic showing various Medical Device Embedded System Engineer job openings in Fall River, MA as of August 2026, with employment types broken down into 1% As Needed, 77% Full Time, 17% Part Time, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution, with an average salary of $137,801 per year, or $66.3 per hour.

Manufacturing Engineer - Medical Device

Volto USA

Raynham, MA • On-site

$75K - $97K/yr

Contractor

Re-posted 25 days ago


Job description

About the Role

We are seeking a Manufacturing Engineer with experience in medical device or regulated manufacturing environments to support manufacturing process development, validation, and production readiness activities. The ideal candidate will have hands-on experience with validation protocols, process engineering, equipment commissioning, and cross-functional collaboration in a highly regulated environment.

This role requires strong technical writing skills, process validation expertise, and the ability to support manufacturing operations, quality initiatives, and continuous process improvements.

Key Responsibilities
  • Author and execute validation protocols and reports including IQ, OQ, and PQ
  • Develop and implement manufacturing processes and production procedures
  • Support process studies, investigations, root cause analysis, and corrective actions
  • Update manufacturing specifications, routes, travelers, and procedures within PLM systems
  • Coordinate new asset commissioning and manufacturing readiness activities
  • Collaborate with Operations, Engineering, Quality, Planning, and OpEx teams
  • Work with OEM equipment manufacturers to define user requirements
  • Ensure compliance with FDA regulations and quality system requirements
  • Prepare technical reports, presentations, and manufacturing documentation
  • Support continuous improvement and process optimization initiatives
Required Skills
  • Manufacturing Engineering
  • Process Validation
  • IQ/OQ/PQ Protocols
  • Medical Device Experience
  • Root Cause Analysis
  • Technical Documentation
  • FDA Compliance
  • Process Engineering
  • PLM Systems
  • Microsoft Office
Preferred Qualifications
  • Experience with machining or metal finishing processes
  • Laser processing or automation experience
  • Knowledge of Minitab and statistical analysis tools
  • Understanding of GD&T principles
  • Experience working in regulated manufacturing environments
  • Ability to support global projects and travel as required
Qualifications
  • 2–4 years of manufacturing or process engineering experience
  • Bachelor’s degree in Engineering or related discipline preferred
  • Strong communication and interpersonal skills
  • Ability to work effectively with cross-functional teams
Preferred Industry Experience
  • Medical Devices
  • Regulated Manufacturing
  • Production Automation
  • Manufacturing Operations