Pharmacovigilance Associate - Markham (Hybrid -12pm-8pm)

The Pharmacovigilance (PV) Associate is a hybrid role based at our Markham facility, with a scheduled shift of 12:00 p.m. to 8:00 p.m. Key responsibilities include managing the collection, processing, and reporting of Adverse Events (AEs) and Product Complaints in compliance with organizational and national pharmacovigilance requirements. The role also includes assisting with Quality Management System (QMS) administration to support compliance with GxP regulations.