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Senior Quality Technologist

Job in London, Ontario, K5Z, Canada
Listing for: Trudell Medical International
Full Time position
Listed on 2025-12-30
Job specializations:
  • Quality Assurance - QA/QC
    Quality Engineering, Quality Control / Manager, QA Specialist / Manager
Salary/Wage Range or Industry Benchmark: 30000 - 60000 CAD Yearly CAD 30000.00 60000.00 YEAR
Job Description & How to Apply Below

Trudell Medical International Inc., 725 Baransway Drive, London, Ontario, Canada

Job Description

Posted Friday, November 7, 2025 at 5:00 AM

At Trudell Medical International (TMI), we pride ourselves on our passion for finding innovative and creative solutions which has enabled us to develop medical devices that continue to make a difference in the lives of people around the world. Situated within a modern facility located in beautiful London, Ontario, TMI offers a comfortable work environment with a respectful and family-oriented culture.

As an employee of Trudell Medical International, not only will you contribute to the development of products at the cutting edge of medical device technology, but you will also have the opportunity to perform challenging work alongside a first-rate group of dedicated professionals.

We’re actively searching for our next team member for the position of:

Senior Quality Technologist

Purpose: Provide technical leadership and support to Quality Technologists and Quality Inspectors in maintaining and developing measurement techniques and plans to support current and new development programs. Set an example for high quality services when communicating with internal teams and external customers/suppliers. Administer, review, and maintain quality system documents. Contribute to general problem solving activities and process improvement initiatives.

RESPONSIBILITIES INCLUDE:

NEW and ongoing product support

  • Measure parts for suppliers and Product Development staff, as required
  • Communicate with suppliers on measurement issues, as required
  • Conduct Inspection Requests
  • Ensure that measurement plans are reviewed, generated, and maintained
  • Ensure that measurement plans are agreed to with suppliers
  • Ensure to review PPAP documentation for completeness and accuracy, highlighting issues prior to forwarding for approval
  • Process:
    Lead the development of fixtures as necessary, working with external resources (suppliers) or internal resources (engineers, quality specialist or level 3 technologist)
  • Process:
    Develop OGP Smart Scope routines
  • Process:
    Troubleshoot OGP Smart Scope routines
  • Process and Systems:
    Troubleshooting of automated QA equipment
  • Process and Systems:
    Support implementation of automated QA equipment
  • Process and Systems:
    Lead investigation of new measurement equipment and methods

incoming and in-process inspection

  • Perform required incoming inspection with calibrated measurement equipment according to measurement plans
  • Perform in-process inspections leading to the release of components and finished goods as required
  • Ensure all products are assembled following Assembly Procedures, Standard Operating Procedures, Good Manufacturing Practices, and in accordance with the Quality Policy Objectives
  • QMS and Systems:
    Lead investigations related to product and processes (non-conformance reports (NCRs), temporary deviations (TDs), and corrective and preventative action (CAPAs)) by gathering and analyzing data and resolving or facilitating resolution
  • QMS and Systems:
    Lead documentation and resolution of non-conformance reports (NCRs) and temporary deviations (TDs) by preparing NCRs and routing them for approval and review TDs and adjust inspections accordingly

data analysis

  • Use quality tools and practices for data analysis, e.g. 5 Why’s, root cause analysis, Pareto charts, statistical techniques, etc.
  • Ensure to prepare and distribute reports on data analysis
  • Process:
    Lead correlation studies and provide analysis and recommended actions
  • Process:
    Extract and analyze data from multiple sources, including SQL databases
  • Perform Gauge Repeatability and Reproducibility (GR&R), as required and generate records
  • Perform Gauge calibration, as required, and generate records
  • Ensure to manage calibration records in Gage Trak, as required
  • Ensure to generate, document, and maintain calibration procedures as required

departmental support

  • Participate in external audits as required by writing audit reports and issuing corrective actions
  • Participate in cross-functional teams as a Quality representative, including Supplier Quality, and Engineering, as required
  • Lead Quality development programs with the focus on continuous improvement
  • Lead…
Position Requirements
10+ Years work experience
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