Medical Device Quality Control (QC) Inspector

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profile Job Location:

Mississauga - Canada

profile Monthly Salary: Not Disclosed
Posted on: 30+ days ago
Vacancies: 1 Vacancy

Job Summary

Department: Quality and Regulatory

Reports to: Quality Control Team Lead

Location: On-site at 3505 Laird Road Mississauga Ontario

Status: Permanent Full-time

Closing date: October 9 2025

Duties and Responsibilities:

  • Inspect test and sample materials parts and products at all stages of manufacturing for defects and any deviations from specifications.
  • Reject and quarantine unacceptable or failing parts initiating non-conformance material reports when required.
  • Observe and monitor manufacturing operations to ensure conformance to procedures and to recommend process improvements.
  • Awareness of product failure modes and customer complaints. Communication of such issues to manufacturing personnel.
  • Assist supervisor in training manufacturing technicians on device defects that may occur from the improper performance of their specific jobs.
  • Follow relevant aspects of good manufacturing practices and the companys quality system with respect to document and record controls material identification and traceability control of nonconforming materials and deviations.
  • Review and approve batch records production documentation and quality control records to ensure completion accuracy and adherence to good documentation practices.
  • Raise issues to manufacturing and QA supervisors about any abnormality in the goods low yield or recurring rejects.
  • Assist production team with cleaning and housekeeping activities in the manufacturing environment.
  • Conduct ongoing and thorough inspections and audits of production processes equipment and documentation to identify any deviations from GMP standards and company procedures.
  • Other duties as assigned.

Qualifications :

Education:

  • A high school diploma is required.
  • Post-secondary diploma in a technical or quality-related field would be an asset.

Experience:

  • 1-2 years of experience working in a regulated manufacturing environment (e.g. medical devices pharmaceutical food automotive etc.)
  • Experience working in a cleanroom/controlled environment is an asset.
  • Experience working with computerized document control systems.

Skills:

  • Attention to detail.
  • Ability to read and understand engineering drawings and specifications.
  • Ability to read and interpret instructions and communicate effectively (verbally and written).
  • Hands-on experience with Excel office 365 applications and SharePoint.
  • Strong work ethic and passion to learn and contribute as a member of a high performing team.
  • Excellent communication and organization skills.
  • Strong interpersonal skills

Remote Work :

No


Employment Type :

Full-time

Department: Quality and RegulatoryReports to: Quality Control Team LeadLocation: On-site at 3505 Laird Road Mississauga OntarioStatus: Permanent Full-timeClosing date: October 9 2025Duties and Responsibilities:Inspect test and sample materials parts and products at all stages of manufacturing for de...
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About Company

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The University Health Network, where “above all else the needs of patients come first”, encompasses Toronto General Hospital, Toronto Western Hospital, Princess Margaret Cancer Centre, Toronto Rehabilitation Institute and the Michener Institute of Education. The breadth of research, t ... View more

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