Quality Control Associate

Universityhealthnetwork; Mississauga; On-site; CAD 45,000 - 55,000; Full time

Job summary

Traferox Technologies Inc. in Mississauga is seeking a Temporary Full-time Quality Control/QA Associate to coordinate inspection records, sample materials, and support GMP-compliant documentation.

The ideal candidate has 1–2 years of experience in a regulated manufacturing environment, exposure to cleanrooms, and proficiency with Excel and SharePoint. This role reports to the Quality Control Team Lead and is based at 2400 Skymark Avenue.

Qualifications

• High School diploma required; post-secondary diploma in a quality-related field would be an asset.
• 1-2 years experience in a regulated manufacturing environment (e.g., medical devices, pharmaceutical, food, automotive).
• Experience working in a cleanroom/controlled environment is an asset.
• Experience working with computerized document control systems.

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.

Skills

Attention to detail

Eng. drawings & specs

Read & interpret instructions

Excel & SharePoint

Work ethic & willingness to learn

Excellent communication

Interpersonal skills

Education

High School diploma

Post-secondary diploma (asset)

Tools

Microsoft Excel

SharePoint

Job description

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 specifications


• Ability to read and interpret instructions and communicate effectively (verbally and written).


• Hands-on experience with Microsoft Excel 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

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.