Lead regional pharmacovigilance operations at Lilly, applying quality systems and regulatory expertise across aligned affiliates and countries.
As Associate Director or Director, you will translate global pharmacovigilance strategy into consistent regional execution. The work spans adverse event management, reporting, risk management, inspections, and Pharmacovigilance System Master File activities. You will connect affiliate safety teams with Global Patient Safety, Qualified Persons for Pharmacovigilance, and the Medical Quality Organization.
Key Responsibilities: Lead, develop, and motivate regional pharmacovigilance personnel
Maintain Lilly's regional pharmacovigilance system across affiliates
Oversee adverse event management and regulatory reporting activities
Monitor quality metrics,



investigate gaps, and drive CAPAs
Represent pharmacovigilance expertise in decision-making forums
Requirements: Bachelor's degree or higher in a relevant field
Minimum five years of pharmaceutical industry pharmacovigilance experience
Experience leading teams across affiliates or geographies
Regulatory agency inspection experience
Ability to travel as needed, approximately twenty percent
Apply regional leadership, regulatory knowledge, and quality expertise to strengthen pharmacovigilance execution across Lilly affiliates.

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📌 Regional Pharmacovigilance Director (Ontario)
🏢 Eli Lilly
📍 Ontario