MD/IVD Regulatory Affairs Specialist
This role will support in defining Regulatory Affairs needs worldwide, focusing more particularly on the critical assessment of key country-specific requirements during all product life cycle stages, and highlighting the differences that may influence or impact companies’ strategy to enter in the market

Magellan is the first cloud-based compliance platform for Medical Devices and IVD products.

The Regulatory Affairs Specialist will play a key role in the development and update of Regulatory Intelligence information. This role will support in defining Regulatory Affairs needs worldwide, focusing more particularly on the critical assessment of key country-specific requirements during all product life cycle stages, and highlighting the differences that may influence or impact companies’ strategy to enter in the market (i.e. pre-market submission requirements, Quality Management System certification acceptance, business/local representative requirements, etc.).

The Regulatory Affairs Specialist will build a solid experience in healthcare products Regulatory Intelligence worldwide.

 

Responsibilities and Duties

Development and maintenance of Medical Device and IVD Regulatory Intelligence Database contents

Customer and Internal support

Others

 

Knowledge, skills and qualifications

 

This is a full-time position located in Vancouver. If you are interested in applying to this position, please contact us at [email protected]