Teams at Regeneron

Provide GMP quality oversight and act as Deputy Responsible Person for batch compilation, review, disposition, and release of biologic products in Canada. Manage quality documentation (Change Controls, Deviations, CAPAs, SOPs, APQRs), monitor quality metrics, oversee importation/distribution and 3PLs, support Health Canada inspections and audits, resolve complex compliance issues, and collaborate with global Quality teams to drive continuous improvement.

Lead and execute commercial launch planning across international markets 12-18 months prior to launch. Define scope, resources, and budgets; coordinate cross-functional stakeholders; build and track timelines, risks, and dependencies; run kick-offs and governance; escalate critical issues and provide leadership updates.

Lead global pharmacovigilance operations by defining governance, ensuring compliance and quality across regions, shaping regional-to-global responsibilities, driving strategic priorities, building high-performing teams, and integrating innovative technologies including AI.