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Quality Engineer

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Profound Medical

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Location:
Canada , Mississauga

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Category:
Manufacturing

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Contract Type:
Not provided

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Salary:

90000.00 - 100000.00 CAD / Year
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Job Description:

The Quality Engineer is responsible for overseeing Quality Improvements across Manufacturing and R&D to ensure product quality and consistency, improve efficiency, and drive value throughout the business. Quality Engineer helps to identify areas of improvement and ensure compliance to the Profound QMS, relevant regulations and standards.

Job Responsibility:

  • Contribute to a positive work culture and foster a high-performance team environment
  • Collaborate with stakeholders across departments to identify areas of improvement and implement quality improvements
  • Investigate Complaints, Returned products & Non- Conformities
  • Improve In-Process and Incoming Inspection testing
  • Work with the Manufacturing & Operations teams to improve the Capital Equipment and Disposables lines
  • Identify opportunities for tools, fixtures & process improvements
  • Work with stakeholders to create and deploy fixtures & tooling
  • Understand current QMS processes and implement procedure improvements to expedite projects and improve compliance
  • Manage product requirements and ensure traceability
  • Participate in risk management activities, including the identification and mitigation of potential quality risks
  • Ensure processes are set up to encourage adherence to QMS
  • Travel as required to support business activities
  • Other duties as assigned

Requirements:

  • University degree in Engineering or Science
  • or relevant work experience
  • P. Eng is an asset
  • 5+ years of experience working in a regulated industry (medical, automotive, aerospace, etc.)
  • Experience working in a clean room
  • Proven examples of fixture/tool implementation projects which deliver meaningful results to the business
  • Experience working on projects in a regulated environment
  • medical device development experience is an asset
  • Experience transferring designs from engineering to manufacturing
  • Experience operating in a quality environment such as GLP, GMP, GCP, ISO 13485 or equivalent
  • Able to work well in teams and independently
  • Detail-oriented
  • highly motivated
  • patient and diligent
  • Excellent problem-solving skills
  • Clear, concise and thorough documentation
  • Excellent verbal and written communication skills
  • Valid passport for travel to United States and Europe

Nice to have:

  • P. Eng is an asset
  • medical device development experience is an asset
What we offer:
  • group RRSP
  • medical benefits paid by the employer

Additional Information:

Job Posted:
March 21, 2026

Employment Type:
Fulltime
Work Type:
On-site work
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