Job Title: Quality Control (QC) Associate

Location: Scarborough, Ontario. Close by the major intersection of Lawrence & Morningside.

Shift: Monday to Friday, 7:00 am - 3:30 pm

Pay Rate: $20.00/hr

Employment Type: Temp to Perm.

Assignment Information

Our client located in Scarborough; Ontario is looking to hire a Quality Control (QC) Associate position. This position will be responsible for ensuring that all finished goods are compliant with the client's quality control standards & policies and making sure to meet their high level of customer service. This position will report to the QA Manager/QA Lead.

Responsibilities:

• Perform incoming inspection for components and base products.
• Verify correct base products and components needed for production before production starts. Ensure all base product pallets have QC incoming blue stickers.
• Verify pre-production inspection to ensure that the production line is clean, clear and free from previous products and components that belong to other projects.
• Verify that all training requirements are completed before production starts and sign off training records on the line.
• Ensure GMP practices are followed on the line and report any GMP violations to Line Leads/Production Supervisor and QA Leader.
• Verify the first-off production sample before production starts and ensure the approved sample is visible to all workers.
• Perform in-process inspection to ensure no defects are detected during production.
• Perform the official release of products from the line and ensure every pallet produced is checked according to the co-packing procedure. All pallets have pallet tags and QC green stickers.
• Effectively inspect products and report any defects found to the Line Lead/Production Supervisor and QA Leader.
• Perform Final Inspection for pallets ready to ship out.
• Perform pre-production inspection for components, when needed.
• Completes all Quality Management System records at all stages of production and inspection.
• Any other assignments as needed.

Requirements:

• College diploma or equivalent experience.
• Minimum 3 years of related experience.
• Experience with developing/documenting procedures.
• Computer proficient.
• Knowledge of GMPs
• Quality orientation and attention to detail.
• Excellent interpersonal and communication skills.
• Problem analysis and problem resolution skills.
• Perform all other duties necessary for the position.