Lead Event Deviations, CAPAs, and Change Controls for Sanofi Canada while applying Canadian GMP expertise across regulated activities.
This leadership role owns quality processes for Sanofi Canada’s internal and external partners. You will manage investigations, corrective actions, and planned changes across relevant Sanofi Business units. The position supports Health Canada requirements, imported products, and high-risk GMP activities while influencing stakeholders without authority.
Key Responsibilities: Own centralized Event, Deviation, and CAPA processes
Assess criticality and manage quality escalations
Present investigations and product release decisions during inspections
Oversee documented, traceable product and process changes
Track metrics and lead continuous improvement projects
Requirements: Bachelor’s degree in Science or equivalent
Seven to ten years of pharmaceutical industry experience
Extensive knowledge of Canadian GMPs
Experience with Canadian importation highly preferred
Excellent analytical, communication, and influencing abilities
Apply Canadian GMP, investigation, CAPA, and change control expertise to strengthen Sanofi Canada’s compliant quality operations.