Jobs 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.

The Office Manager coordinates daily office operations, managing vendors, supporting health and safety, and facilitating onboarding while enhancing workplace efficiency.

The Associate Director, Finance & Administration collaborates with leadership on budgeting, forecasting, financial planning, and compliance while managing resource planning and P&L insights.

The Canada Compliance Director leads compliance efforts across Canada, develops policies, coordinates with global teams, and mitigates compliance risks in the pharmaceutical industry.

Lead and manage global aggregate safety reporting (PSURs/PBRER, DSURs, PAER, local reports, SUSARs). Plan, produce, and distribute reports; define data requirements; ensure compliance and quality metrics; oversee CRO/vendor outputs; support inspections and audits; develop SOPs/templates/KPIs; drive process improvement and technology implementations; collaborate with safety, clinical, regulatory, epidemiology, and statistics teams.

Lead regional execution of the enterprise third‑party risk management program: oversee onboarding, due diligence, monitoring, issue remediation, reporting, KPIs/KRIs, and partner with Procurement, Legal, Compliance, IP, and InfoSec. Drive adoption of automation, AI, and analytics in TPRM platforms and develop team capabilities while providing regional governance and escalation for material risks.

Lead global execution of smaller/less complex clinical trials from design to close-out. Manage timelines, budgets, vendor/CRO relationships, study documentation, systems (CTMS/TMF/EDC/IVRS), risk mitigation, site selection/activation, recruitment strategies, database lock and close-out, and supervise Clinical Trial Management staff while driving process improvements and ensuring ICH/GCP and SOP compliance.

Field-based immunology sales role driving brand growth through high-quality HCP engagement, local account planning, cross-functional collaboration, multi-channel communication, and reporting to leadership.

Field-based specialty pharmaceutical representative for immunology in Southwestern Ontario. Drive sales growth, implement brand and local account plans, engage HCPs across multiple channels, collaborate with medical and regional teams, report results, and support launch/start-up activities while traveling within the territory.