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Biomedical Engineer Internship Jobs in Ontario (NOW HIRING)

Junior Planner

Oakville, ON ยท On-site

CA$55K - CA$65K/yr

With an academic background in biomedical, electro-mechanical manufacturing, or business, you are ... Coordinate between suppliers and engineering to facilitate smooth prototype and final build ...

Biomedical Engineer Internship information

See Ontario salary details

$8

$30

$59

How much do biomedical engineer internship jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for biomedical engineer internship in Ontario is $30.65, according to ZipRecruiter salary data. Most workers in this role earn between $18.03 and $38.70 per hour, depending on experience, location, and employer.

What does a biomedical engineer intern do?

A Biomedical Engineer Intern typically assists with the design, development, and testing of medical devices and healthcare technologies. Interns may work on projects related to improving medical equipment, analyzing data from clinical trials, or supporting the research and development team. The role often involves collaborating with engineers, scientists, and healthcare professionals to solve real-world problems in medicine. Interns gain hands-on experience and learn about regulatory standards, product development processes, and the application of engineering principles in healthcare.

What are the qualifications to get a biomedical engineer internship?

The primary qualifications for getting a biomedical engineering internship are enrollment in an appropriate degree-seeking field and meeting any other requirements posted by the company offering the internship. Common requirements include having a cumulative GPA at or above a set level, being a citizen or permanent resident of the United States, and the ability to pass a background check. Some companies accept recent graduates. Fulfilling the duties and responsibilities of a biomedical engineer internship requires communication skills, organization skills, and the ability to work independently or collaboratively as needed. Previous experience working in biological research labs can help you stand out from other applicants.

What are the key skills and qualifications needed to thrive as a biomedical engineer intern, and why are they important?

To thrive as a Biomedical Engineer Intern, you need a solid background in biology, engineering principles, and mathematics, often supported by progress toward a bachelor's degree in biomedical engineering or a related field. Familiarity with CAD software, data analysis tools like MATLAB, and laboratory equipment is typically required. Strong problem-solving abilities, attention to detail, and effective teamwork and communication skills help interns excel in collaborative research and development environments. These competencies are crucial for contributing to innovative healthcare solutions and successfully supporting engineering teams.

What types of projects do biomedical engineering interns typically work on, and how do these projects contribute to their learning and future career growth?

Biomedical engineering interns often participate in projects such as designing medical devices, conducting laboratory testing, analyzing clinical data, or assisting with regulatory documentation. These hands-on experiences allow interns to apply classroom knowledge to real-world challenges, develop technical skills, and understand industry standards. Working alongside experienced engineers and healthcare professionals also helps interns build communication and teamwork skills, which are essential for career advancement. Successfully completing an internship can open doors to full-time roles and specialized career paths within biomedical engineering.

What is the difference between Biomedical Engineer Internship vs Biomedical Engineer?

AspectBiomedical Engineer InternshipBiomedical Engineer
Required CredentialsEnrolled in or recent graduate of a relevant degree programBachelor's or higher in biomedical engineering or related field
Work EnvironmentInternship setting, often in labs or hospitalsFull-time professional setting, including labs, manufacturing, or research facilities
Employer & Industry UsageEducational institutions, hospitals, research centersMedical device companies, healthcare institutions, research organizations

The Biomedical Engineer Internship is a temporary, educational position designed to provide hands-on experience, while a Biomedical Engineer is a full-time professional responsible for designing and testing medical devices or systems. Internships serve as a stepping stone toward a career in biomedical engineering, which requires more advanced skills and credentials.

Is there a high demand for biomedical engineer internships?

Biomedical engineer internships are in growing demand due to advancements in medical technology and healthcare needs. Internships often require knowledge of engineering principles, medical devices, and relevant software, making them competitive but accessible for students with technical backgrounds.

What is a typical biomedical engineer internship?

A biomedical engineer internship typically involves assisting with the design, testing, and maintenance of medical devices and equipment. Interns often gain hands-on experience with CAD software, laboratory testing, and regulatory compliance, working under the supervision of experienced engineers in a healthcare or research setting. The internship duration usually ranges from a few months to a summer program, and candidates often need a background in biomedical engineering or related fields.

What are the most commonly searched types of Biomedical Engineer jobs in Ontario?

The most popular types of Biomedical Engineer jobs in Ontario are:

What are popular job titles related to Biomedical Engineer Internship jobs in Ontario?

For Biomedical Engineer Internship jobs in Ontario, the most frequently searched job titles are:

Infographic showing various Biomedical Engineer Internship job openings in Ontario as of August 2026, with employment types broken down into 85% Full Time, 12% Part Time, and 3% Contract. Highlights an 85% Physical, 6% Hybrid, and 9% Remote job distribution, with an average salary of $63,748 per year, or $30.6 per hour.

Systems Engineering Developer (2 Openings)

Intellijoint Surgical

Kitchener, ON โ€ข On-site

Full-time

Medical, Dental, Vision, PTO

Posted 2 days ago

New


Job description

Type of Position: 

Full-Time – 2 Positions 

Location: 

Kitchener, ON – In office 4-days a week 

Benefits: 

RRSP with employer match, health/dental/vision package (day-1 and employer-paid premiums!), wellness benefit, learning & development opportunities, paid vacation, personal days and sick days 

Salary Range: 

$65k - $80k *Individual placement within the salary range will be based on experience, skills, market data, and internal equity considerations 

The Company 

Intellijoint Surgical develops effective, easy-to-use technologies that enhance surgeons’ care and improve patients’ lives. Our technology supports surgeons in the operating room during hip and knee replacement procedures, helping improve surgical outcomes and providing valuable real-world data that informs future innovation.  

Within Intellijoint Surgical is IJX, a business unit focused on commercializing navigation and planning technologies through innovative business models across clinical applications.  

The Positions 

We are hiring 2 Systems Engineering Developers to join our growing Engineering team. Both roles help ensure our systems are designed, tested, validated, and documented to meet user needs, regulatory requirements, and internal quality standards. The key difference between the roles is focus: one role supports commercially released Intellijoint Surgical products, while the other supports IJX innovation and prototyping initiatives. 

Whether your passion lies in bringing new ideas to life, or advancing established products used by surgeons every day, this is an opportunity to make a meaningful impact on patient care! 

These roles are ideal for someone who: 

  • Has strong engineering foundations and experience in medical device development within a regulated environment (ISO 13485). 

  • Understands complex software and hardware systems and can specify, verify, validate and document them with precision. 

  • Enjoys collaborating and solving challenging technical problems across engineering, quality, regulatory, clinical, and business teams. 

  • Is process-oriented, detail-focused, and comfortable with documentation, traceability, and risk management. 

  • Is energized by either early-stage prototyping and innovation or solving complex challenges for commercialized products. 

What You Will Do: 

Systems Design & Engineering 

  • Design and develop system-level solutions that meet user, product, and business requirements. 

  • Create and maintain software and system design specifications in collaboration with development teams. 

  • Lead and participate in system design reviews with cross-functional stakeholders. 

  • Balance quality, cost, risk, usability, and time-to-market considerations in design decisions. 

Role Specific Focus: IJS 

  • Investigate and resolve technical issues identified through field feedback, manufacturing, quality, or supply chain activities. 

  • Develop and implement design changes that improve product performance, reliability, manufacturability, or usability. 

Role Specific Focus: IJX 

  • Prototype system-level concepts, including software, algorithms, and mechanical instrumentation. 

  • Evaluate emerging technologies and contribute to the development of innovative products and clinical applications. 

  • Contribute to advanced algorithm development and testing in areas such as computer vision, medical imaging processing, machine learning, and 3D registration. 

Verification & Validation 

  • Plan, design, develop and execute system-level verification and validation activities. 

  • Plan, conduct, and report on formative and summative validation activities with surgeons, business stakeholders, and other end users. 

  • Document results in engineering reports and formal test documentation. 

  • Maintain traceability between requirements, risks, and verification activities throughout the product lifecycle. 

Design Controls & Documentation 

  • Manage design inputs and outputs, including requirements, specifications, risk management files, and V&V documentation within the Design History File (DHF). 

  • Drive risk management activities, including hazard analysis, risk assessment, and mitigation strategies. 

  • Support patient safety, cybersecurity, and privacy requirements within system designs. 

  • Contribute to Product Instructions for Use (IFU) and related technical documentation. 

  • Ensure compliance with Intellijoint’s Quality Management System (QMS) and participate in continuous improvement initiatives. 

Skills and Experience to Enable Success: 

  • Bachelor’s degree in Computer Science, Software Engineering, Biomedical Engineering, or a related field. 

  • 3-5 years of relevant experience, including applicable co-op or internship experience. 

  • Experience working with software and hardware medical device systems. 

  • Strong familiarity with regulated environments, including ISO 13485 requirements, verification, validation and traceability activities. 

  • Experience with risk management processes under ISO 14971. 

  • Understanding of the medical device development lifecycle and how regulatory requirements influence system design. 

  • Strong technical writing skills and exceptional attention to detail. 

  • Familiarity with software and hardware development concepts, architectures, and lifecycle processes. 

  • Experience with IEC 62304, IEC 62366, and ISO 27001 or similar frameworks. 

  • Experience planning and conducting usability studies and validation activities. 

  • Interest in emerging technologies and solving complex technical challenges. 

Assets: 

  • Experience with surgical navigation, robotics, imaging, planning, or other advanced medical technologies. 

  • Experience developing or evaluating algorithms related to computer vision, machine learning, image processing, or 3D spatial systems. 

Why Join Us? 

  • It is unrealistic for us to believe we will find someone who fits this position 100% - interested? Apply! 

  • Strong support towards career development and growth 

  • Work on innovative products that improve surgical outcomes and enhance patient’s quality of life 

  • Work alongside a highly talented and driven group of team members and colleagues’ organization wide 

  • Work in an environment with high transparency and collaboration along with lots of fun and social activities 

  • Be ok with change and share in our excitement as we scale  

  • Flexibility so that you can do your best both at work and outside of it 

Intellijoint Surgical is committed to creating an accessible and inclusive work environment. It is our policy to recruit and select applicants solely on the basis of their qualifications. We are an equal opportunity employer that hires talent regardless of age, race, creed, colour, religion, national origin, ancestry, marital status, sexual orientation, gender identity or expression, disability, or any other status or condition protected by applicable law. 

Intellijoint Surgical encourages applications from all qualified candidates. Those in need of accommodation at any stage in the recruitment process should notify hr@intellijointsurgical.com. Any information received that relates to accommodation needs of a candidate will be addressed in a confidential manner. 

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