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 reviewProvide quality oversight for commercial and clinical productsCreate and manage quality documentation and change controlsResolve compliance issues using risk-based judgmentOversee logistics and distribution activities in CanadaRequirements:Canadian Bachelor's degree in Life SciencesAt least 5 years of Quality Assurance experienceUnderstanding of GMP environments and Health Canada regulationsStrong collaboration and communication skillsPreferred background in biopharmaceutical importationEnhance your quality assurance career at Regeneron, making a meaningful impact on patient outcomes.#J-18808-Ljbffr