Champion financial leadership for Surgery Canada, driving performance and compliance in a complex, multi-country environment while collaborating with cross-functional teams to execute strategic business initiatives.

Unlock potential by providing strategic CMC regulatory expertise to accelerate the development and lifecycle management of drug-device combination products, ensuring compliance with global regulations and engaging with cross-functional teams.

Elevate your career as a Principal Scientist in CMC Regulatory Affairs, leading strategies for drug-device combination products, guiding cross-functional teams, and ensuring compliance with global regulations to advance healthcare innovations.

Shape regulatory strategies for drug-device combination products, ensuring compliance with global standards while collaborating across teams to support development and lifecycle management in a hybrid role.

Join a team that's committed to driving innovation in regulatory science for drug-device combination products, collaborating cross-functionally to develop and execute strategies for successful global product submissions and lifecycle management.