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Medical Device Quality Control Jobs in Ontario (NOW HIRING)

Actalent

Process Engineer

Mississauga, ON

Utilize vision systems and other inspection technologies to support process control and product quality in a medical device manufacturing environment. * Troubleshoot manufacturing issues on the ...

Aerotek

Medical Device Assembler

Mississauga, ON

CA$19/hr

Quality inspecting medical devices * Completing documentation * Suggesting different ways to better assembly * Testing devices Shift * Day shift * Monday - Thursday * 7:00am - 5:30pm Pay * $19.00 an ...

Profound Medical

Quality Manager, Production

Mississauga, ON · On-site

CA$110K - CA$140K/yr

... control, to gently ablate the diseased tissue with minimal side effects. If you share our values ... EU Medical Device Regulation (MDR), and Canadian Medical Device Regulations (CMDR). * Language ...

BWXT

Quality Control Supervisor

Cambridge, ON · On-site

BWXT Canada's subsidiary, BWXT Medical Ltd. (BWXT Medical) provides its customers, who conduct life ... Position Overview: As our Quality Control Supervisor, you will lead and oversee daily shop ...

BWXT

Quality Control Supervisor

Cambridge, ON · On-site

BWXT Canada's subsidiary, BWXT Medical Ltd. (BWXT Medical) provides its customers, who conduct life ... Position Overview: As our Quality Control Supervisor, you will lead and oversee daily shop ...

BWXT

Quality Control Technician

Kitchener, ON · On-site

BWXT Canada's subsidiary, BWXT Medical Ltd. (BWXT Medical) provides its customers, who conduct life ... As our Quality Control Technician, you will ensure compliance with BWXT's quality program ...

BWXT

Quality Control Technician

Kitchener, ON · On-site

BWXT Canada's subsidiary, BWXT Medical Ltd. (BWXT Medical) provides its customers, who conduct life ... As our Quality Control Technician, you will ensure compliance with BWXT's quality program ...

E3 Works

Quality Control Inspector

Windsor, ON

CA$34/hr

We're hiring a Quality Control Inspector / CMM Programmer in Windsor! * Full time position ... Experience in nuclear, defence, aerospace, or medical manufacturing is an asset * Knowledge of CSA ...

Profound Medical

Senior Software Developer

Mississauga, ON · On-site

CA$120K - CA$160K/yr

... control, to gently ablate the diseased tissue with minimal side effects. If you share our values ... Familiarity with medical device compliance standards and quality management systems is preferred.

VitalBio

QC Technician (3-Month Contract)

Oakville, ON

CA$24 - CA$27.40/hr

... device history and batch production records as well as assisting with the development of work instructions for these activities. What You'll Do: * Execute Quality Control activities in support of ...

Integra

QA/QC Engineer

Cambridge, ON

Toronto Department: DEPCON The Opportunity The QA/QC Engineer supports both electrical and ... Comprehensive healthcare - Medical, dental, and vision coverage that supports you and your family ...

New

Sotera Health

Quality Assurance Specialist

Ottawa, ON · On-site

... top 50 medical device companies and 9 of the top 10 pharmaceutical companies. Reporting to the ... A Nuclear Energy Worker (NEW) is defined by the Nuclear Safety and Control Act as a person who is ...

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Medical Device Quality Control information

What is medical device quality control?

Medical Device Quality Control refers to the processes and procedures used to ensure that medical devices meet safety, quality, and regulatory standards before they reach the market. This involves rigorous inspection, testing, and documentation throughout the manufacturing process to prevent defects and ensure consistent product performance. Quality control professionals work to identify issues, monitor compliance with industry regulations like ISO 13485 and FDA requirements, and help maintain the integrity of healthcare products. Their role is crucial in protecting patient safety and upholding the reputation of medical device manufacturers.

What are the key skills and qualifications needed to thrive as a medical device quality control professional?

To thrive in Medical Device Quality Control, you need a solid understanding of quality assurance principles, regulatory standards (such as ISO 13485 or FDA 21 CFR Part 820), and experience with inspection techniques, often supported by a degree in engineering or life sciences. Familiarity with tools like statistical process control (SPC) software, electronic quality management systems (eQMS), and documentation protocols is typical. Attention to detail, problem-solving abilities, and strong communication skills are essential soft skills for excelling in this role. These competencies are crucial for ensuring product safety, regulatory compliance, and maintaining the reputation of the medical device manufacturer.

What are some common challenges faced in a medical device quality control role, and how can I prepare for them?

Professionals in Medical Device Quality Control often face challenges such as keeping up with evolving regulatory standards, managing documentation for audits, and ensuring consistent product quality across batches. To prepare, it's helpful to develop strong attention to detail, stay updated on FDA and ISO guidelines, and build effective communication skills to collaborate with cross-functional teams like manufacturing and R&D. Being proactive in identifying potential risks and participating in continuous improvement initiatives can also help you succeed in this role.

What is the difference between Medical Device Quality Control vs Medical Device Quality Assurance?

AspectMedical Device Quality ControlMedical Device Quality Assurance
FocusInspecting and testing products to identify defectsDeveloping and maintaining quality systems and processes
ActivitiesProduct testing, inspection, samplingAudits, process validation, compliance management
CertificationsISO 13485, GMP trainingISO 13485, regulatory standards
Work EnvironmentLaboratories, manufacturing floorsQuality departments, regulatory offices

Medical Device Quality Control focuses on testing and inspecting products to ensure they meet quality standards, while Medical Device Quality Assurance emphasizes establishing systems and processes to prevent defects and ensure compliance. Both roles are essential in maintaining high-quality medical devices and often work closely within the industry.

What are popular job titles related to Medical Device Quality Control jobs in Ontario?

For Medical Device Quality Control jobs in Ontario, the most frequently searched job titles are:

What job categories do people searching Medical Device Quality Control jobs in Ontario look for?

The top searched job categories for Medical Device Quality Control jobs in Ontario are:

What cities in Ontario are hiring for Medical Device Quality Control jobs?

Cities in Ontario with the most Medical Device Quality Control job openings:

Medical Device Quality Control jobs near you
Infographic showing various Medical Device Quality Control job openings in Ontario as of August 2026, with employment types broken down into 1% As Needed, 72% Full Time, 21% Part Time, and 6% Contract. Highlights an 92% Physical, 1% Hybrid, and 7% Remote job distribution.

Medical Device Engineer - Intermediate

Smarter Alloys

Cambridge, ON • On-site

Full-time

PTO

Re-posted 16 days ago

Key responsibilities

  • Design, build, and test medical devices and applications for the medical industry.

  • Own projects from concept through to production, including planning, execution, and cross-department collaboration.

  • Perform material characterization, mechanical testing, and validate test setups for device and material performance.

Job description

Medical Device Engineer – Intermediate You're an experienced engineer looking for your next challenge, where you can take full ownership of technical projects, push the boundaries of smart materials innovation, and contribute meaningfully to a growing company. Smarter Alloys is that company, and this is that role. Who We Are Smarter Alloys is at the forefront of the smart materials revolution. Our programmable shape memory alloy technology is powering advancements in industries from medical and dental to automotive, consumer electronics, and sporting goods. We are a dynamic, fast-moving company with big ambitions and the technology to back them up. The Role We are seeking an Intermediate Medical Device Engineer to design, build, and test devices and applications for the medical industry. You will own your projects from concept through to production, with responsibility for planning, execution, and collaboration across departments. This is a hands-on role for someone who thrives in a startup environment, ready to lead technical development, solve complex problems, and help drive innovation forward. Key Responsibilities * Lead the end-to-end development of medical devices using advanced shape memory alloys. * Support and contribute to the Quality Management System (ISO 13485). * Translate high-level concepts into manufacturable designs through rapid prototyping and iteration. * Perform material characterization and mechanical testing under ISO/ASTM standards. * Design and validate test setups for device and material performance. * Collaborate cross-functionally with procurement, quality, production, and business development teams. * Contribute to strategic development planning and continuous improvement initiatives. * Guide or mentor junior team members when needed. Qualifications * Bachelor's degree in Materials, Mechanical, or Biomedical Engineering. * 3+ years of experience in medical device development within a regulated environment. * Strong understanding of ISO 13485, FDA regulations, and QMS documentation. * Demonstrated ability to manage projects independently from concept through production. * Proficient in mechanical design principles, GD&T, and manufacturing processes. * Hands-on experience with mechanical testing and data interpretation. Assets (Nice-to-Haves) * Experience with 3D CAD tools such as SolidWorks or AutoDesk. * Background in shape memory alloys or advanced materials. * Familiarity with laser processing and other precision manufacturing technologies. * Demonstrated ability to make data-driven design decisions and optimizations. Working @ Smarter Alloys This is a full-time, permanent position based in our state-of-the-art Cambridge, ON facility. We offer a competitive compensation package, full benefits, paid vacation, and the opportunity to be part of something cutting-edge. We value diversity and are committed to building a team that reflects the community we serve. We encourage applications from women, visible minorities, Indigenous peoples, LGBTQ2SI individuals, veterans, and persons with disabilities. Accommodations are available upon request for all parts of the recruitment process.