CPL seeks a Supplier Quality Specialist I to enhance quality control processes in pharmaceutical manufacturing through effective sampling and inspections. Excellent attention to detail is required.

As a Supplier Quality Specialist, you will be involved in the inspection of packaging materials and raw substances. Candidates must have at least two years in pharmaceutical manufacturing and will manage sampling and third-party testing orders. Your role is essential in ensuring compliance and improving quality processes.

Key Responsibilities:
• Inspect incoming raw materials and packaging components
• Perform ID testing using TruScan
• Create and manage purchase orders for testing
• Supervise storage and destruction of retention samples
• Implement improvements in sampling efficiency

Requirements:
• Two-year college diploma in a scientific field
• Minimum 2 years pharmaceutical experience required
• Proficient understanding of cGMP regulations
• Capable in SAP and Microsoft Excel
• Effective verbal and written communication skills

Uphold quality standards and contribute to CPL's mission of excellence in pharmaceutical product manufacturing.
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📌 Supplier Quality Specialist I at CPL (Ontario)
🏢 Contract Pharmaceuticals
📍 Ontario