Elevate your career as a Quality Systems Specialist with Iovate Health Sciences! This role focuses on regulatory compliance and quality assurance in a agile setting in Milton, Ontario.

As an essential member of the Quality Assurance team, you'll utilize your expertise to support ingredient approval and maintain product safety. Your duties will encompass overseeing stability programs, managing quality complaints, and engaging with product development teams to implement corrective actions. Collaboration and independence are vital.

Key Responsibilities:
• Collaborate with Quality Assurance team for compliance
• Lead and manage the Stability Program testing
• Oversee ingredient approval and quality claims




• Execute the Change Control process effectively
• Draft Certificates of Analysis and Finished Specifications

Requirements:
• 4 years of QA experience within manufacturing
• Bachelor's level education in scientific discipline
• Understanding of GMP regulations and quality systems
• Excellent detail orientation and organizational skills
• Strong knowledge of Microsoft Office applications

Utilize your skills in quality assurance at Iovate and promote product safety and compliance!
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📌 Iovate Quality Systems Specialist Role (Ontario)
🏢 Iovate
📍 Ontario