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Medical Device Embedded System Engineer Jobs in Toronto, ON

Hitachi Rail is looking an enthusiastic and self-motivated Signaling System Engineer who thrives in ... Medical, Dental and Vision Insurance, Long Term Disability, Life & Accident Insurance,a ...

Collaborate with our hardware, safety and systems teams on design, build and validation of highly ... An experienced (5+ years) developer who codes embedded software on low level ARM microcontrollers ...

... and embedded systems. Grounded in a culture of innovation and collaboration, we believe real ... Interface between AMD and external Power Delivery, Retimer and Device vendors to enable, debug and ...

... and embedded systems. Grounded in a culture of innovation and collaboration, we believe real ... Interface between AMD and external Power Delivery, Retimer and Device vendors to enable, debug and ...

... System (QMS), ensuring compliance with ISO 13485, FDA QMSR, MDSAP, Health Canada Medical Device ... Bachelor's degree in Engineering, Life Sciences, Biomedical Engineering, Quality, or a related ...

New

Senior Software Developer

Mississauga, ON · On-site

CA$120K - CA$160K/yr

General Accountability The Senior Software Developer is responsible for designing and delivering ... Familiarity with medical device compliance standards and quality management systems is preferred.

Showing results 41-60

Medical Device Embedded System Engineer information

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 are popular job titles related to Medical Device Embedded System Engineer jobs in Toronto, ON?

For Medical Device Embedded System Engineer jobs in Toronto, ON, the most frequently searched job titles are:

What job categories do people searching Medical Device Embedded System Engineer jobs in Toronto, ON look for?

The top searched job categories for Medical Device Embedded System Engineer jobs in Toronto, ON are:

Infographic showing various Medical Device Embedded System Engineer job openings in Toronto, ON as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 12% Part Time, and 5% Contract. Highlights an 91% Physical, 1% Hybrid, and 8% Remote job distribution.

Senior Electrical Developer

Mississauga, ON • On-site

CA$110K - CA$140K/yr

Full-time

Re-posted yesterday


Job description

Our mission is to Profoundly change the standard of care by creating a tomorrow where clinicians can confidently ablate tissue with precision; a tomorrow where patients have access to safe and effective treatment options, so they can quickly return to their daily lives. Changing the standard of care is part of our fabric. We are a group of energetic, problem-solvers focused on innovation, and looking to change the world. We are changing the paradigm for treating diseases such as prostate cancer by using real-time MR Imaging, thermal ultrasound and close-loop temperature feedback control, to gently ablate the diseased tissue with minimal side effects.


If you share our values and want to work in a collaborative results focused culture and want to make a Profound impact in healthcare and your career, here is your chance.


General Accountability

We are seeking a Sr. Electrical Developer to design and develop electronics for medical devices. The role is responsible for designing mixed analog and digital circuitry, debugging system-level issues, and owning electrical system specifications and verification test cases - ensuring designs are robust, well-documented, and verified to meet requirements and quality standards.


Duties and Responsibilities

  • Design mixed analog and digital (mixed-signal) circuitry - schematic capture in Altium Designer, topology selection, and design analysis - for new and sustaining medical-device products.
  • Own electrical system specifications, defining and maintaining electrical requirements, interface definitions, and design documentation.
  • Develop and own electrical verification test cases and protocols, and execute or oversee verification testing to demonstrate that requirements are met.
  • Debug and root-cause complex system-level issues spanning analog, digital, power, firmware, signal-integrity, and communication domains.
  • Perform circuit analysis and simulation (e.g., SPICE), including worst-case, tolerance, timing, and power analyses, to ensure robust designs.
  • Guide PCB layout and review schematics and layouts for signal integrity, EMC, grounding/shielding, thermal, and manufacturability.
  • Select and specify components, create and manage bills of materials, and evaluate parts for performance, reliability, and lifecycle.
  • Bring up, characterize, and troubleshoot prototypes using oscilloscopes, logic analyzers, spectrum analyzers, multimeters, and other laboratory equipment.
  • Collaborate with firmware, mechanical, systems, and software engineers to integrate electronics into the overall system.
  • Contribute to design reviews, risk management (dFMEA), and design-for-test and design-for-manufacture activities.
  • Author and maintain design documentation, analyses, and reports to satisfy design-control and regulatory requirements.
  • Support manufacturing and suppliers with technical issues, design transfer, and continuous improvement.


Education

Bachelor's degree in Electrical Engineering, Electronics Engineering, or a related discipline; advanced degree an asset.


Key Attributes

Required:

  • 7+ years of electronics design experience, including hands-on mixed-signal (analog and digital) circuit design.
  • Strong analog design skills (amplifiers, filters, data acquisition, power, and sensor interfaces) together with digital design (microcontrollers, memory, and communication buses).
  • Proven ability to debug complex, system-level hardware issues to root cause across multiple domains.
  • Experience defining electrical requirements and specifications and developing verification test cases and protocols.
  • Proficiency with Altium Designer for schematic capture and PCB design, and with circuit simulation tools (e.g., SPICE).
  • Hands-on proficiency with laboratory test and measurement equipment (oscilloscopes, logic and spectrum analyzers, multimeters).
  • Strong understanding of signal integrity, grounding, shielding, and EMC principles.
  • Excellent documentation and communication skills.

Desired:

  • Experience in a regulated medical-device environment (FDA 21 CFR 820, ISO 13485, ISO 14971, IEC 60601).
  • Familiarity with EMC and electrical-safety testing and certification (IEC 60601-1, IEC 60601-1-2).
  • Firmware or embedded software experience (C or C++).
  • Experience with low-noise power amplifiers
  • MRI-compatible hardware, non-ferromagnetic design, or medical-imaging systems experience.
  • FPGA or programmable-logic design experience.
  • Design for manufacturability and test, tolerance analysis, and supplier management.



We thank you for your interest in Profound Medical. Please note only candidates that are short-listed will be contacted.


The expected annual salary range for this role is $110,000 - $140,000 CAD. Actual compensation will be determined based on experience, qualifications, and job-related factors. This role may also be eligible for participation in the company's benefits programs, such as a group RRSP and medical benefits paid by the employer.


We strive to promote diversity and equal opportunity in the workplace and encourage applications from all qualified individuals, including those with disabilities. If selected to participate in the recruitment, selection, and/or assessment process, please inform Human Resources of the nature of any accommodation(s) that you may require.