Description
Teva is hiring a Regulatory Affairs Manager in Montreal, Quebec for a hybrid role requiring three days on site. The position leads Canadian regulatory planning and execution for innovative medicines, oversees Health Canada submissions and regulatory strategy for clinical development programs and product registrations, and manages CTAs, NDSs, SNDSs, labelling updates, compliance reviews, pharmacovigilance reporting, and regulatory meetings with Health Canada. The role requires a science-related bachelor’s degree, preferred master’s degree, at least five years of pharmaceutical industry experience, strong Health Canada and ICH knowledge, and demonstrated leadership in submissions and cross-functional project work.
