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Quality Control Associate @ University Health Network

CAOnsiteContractJob reference REF12792B
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About this role

Union: Non-Union

Number of Vacancies: 1

New or Replacement Position: Replacement

Site: 2400 Skymark Avenue, Mississauga

Department: Quality and Regulatory

Reports to: Quality Control Team Lead

Salary Range: $45,000 - $55,000 annually

Hours: 37.5 Hours Per Week

Shifts: Days, Monday - Friday

Status: Temporary Full-time (12-month contract)

Closing Date: Open until filled

Duties and Responsibilities:

Coordinate the incoming activities with production, reviewing, approving and archiving inspection records and issuing nonconformances as required.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.Follow relevant aspects of good manufacturing practices and the company’s 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.Prepare product release documentation to release finished goods into inventory.Assist in reviewing and approving production shipment paperwork, records and creating distribution records in electronic database.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.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.Other duties as assigned. 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 experience 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 specificationsAbility to read and interpret instructions and communicate effectively (verbally and written).Hands-on experience with Microsoft Excel and SharePointStrong work ethic and passion to learn and contribute as a member of a high performing team.Excellent communication and organization skillsStrong interpersonal skills We thank all applicants for their interest in this position with Traferox Technologies Inc. Please note that only candidates selected for an interview will be contacted.

Skills

ManufacturingAssociateMedical Device

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