Regulatory Quality Specialist — ISO 9001 & MDR

A global leader in in vitro diagnostics is seeking a Regulatory Compliance Specialist in Saint-Laurent-de-l'Île-d'Orléans, Canada. The role focuses on ensuring compliance with Canadian Medical Devices Regulations and ISO 9001 requirements. Candidates should possess a Bachelor’s degree in Science, Biology or Quality, along with strong Microsoft Office skills and 2+ years of experience in the Medical Devices Industry.

This role requires strong communication and collaboration skills as well as the ability to work in a dynamic international environment.