Join Regeneron as an Associate Manager in Quality Assurance, working hybrid from Toronto. Focus on GMP oversight and biologic product distribution compliance for Canada.

In this pivotal role at Regeneron, you will provide quality assurance support within a globally focused team. You’ll act as the Deputy Responsible Person for batch management and collaborate with various stakeholders, including regulatory authorities. Your role will be vital in maintaining high quality and compliance standards across our biologics portfolio.

Key Responsibilities:
• Oversee batch disposition and approval for Canadian products
• Develop and manage key quality documentation processes
• Ensure adherence to Health Canada inspection requirements




• Monitor compliance through quality system metrics
• Support collaboration across Quality teams globally

Requirements:
• Canadian Bachelor's degree in Life Sciences required
• At least 5 years of experience in Quality Assurance
• Knowledge of GMP and GDP principles essential
• Demonstrated ability to manage complex quality issues
• Experience with biologic importation preferred

Utilize your expertise to enhance quality assurance and regulatory compliance at Regeneron, impacting patients positively.
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📌 Hybrid Associate Manager for Quality Assurance (Ontario)
🏢 Initial Therapeutics
📍 Ontario