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...
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
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