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 settings 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.