Make a difference as a Technical Information Associate in Coquitlam, focusing on quality control and regulatory compliance. This full-time role offers an exciting way to contribute to our health brands.

In this permanent position, you will assist the QC group by evaluating supplier data and updating specifications for pharmaceutical products. Your duties will include submitting necessary change controls, coordinating quality testing, and creating operating procedures. A deep understanding of regulatory guidance from various health product authorities is also important for this role.

Key Responsibilities:
• Submit change controls to improve specifications
• Coordinate stability pulls for sampling
• Maintain accuracy in product specifications
• Create and revise operating procedures effectively
• File and organize technical documents diligently

Requirements:
• Bachelor’s degree or technical diploma in science
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