Join Regeneron as an Associate Manager of Quality Assurance, focusing on the oversight of biologics importation for Canada. This hybrid position emphasizes GMP compliance and collaboration with quality teams.

Located in Toronto, this role includes being the Deputy Responsible Person while ensuring the timely disposition of biologic products. You'll create and revise key quality documentation while monitoring essential compliance metrics. Engage with local and global stakeholders to foster improvements in quality practices within a science-focused organization.

Key Responsibilities:
• Act as Deputy Responsible Person in product review
• Provide quality oversight for commercial and clinical products
• Create and manage quality documentation and change controls




• Resolve compliance issues using risk-based judgment
• Oversee logistics and distribution activities in Canada

Requirements:
• Canadian Bachelor's degree in Life Sciences
• At least 5 years of Quality Assurance experience
• Understanding of GMP environments and Health Canada regulations
• Robust collaboration and communication skills
• Preferred background in biopharmaceutical importation

Enhance your quality assurance career at Regeneron, making a meaningful impact on patient outcomes.
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📌 Quality Assurance Associate Manager Role (Ontario)
🏢 Regeneron
📍 Ontario