Primary Functions:

The Manager of Regulatory Affairs is responsible for formulating, managing and executing strategies in order to achieve the objectives of the Regulatory Department. This could include management of regulatory staff and regulatory consultants who may undertake specific projects of both a medical and regulatory nature. The Manager is also responsible for developing and maintaining a close working relationship with Marketing, Sales, Quality Assurance, Project Management, Business Development, Clinical Research, Supply Chain Management and Labelling Team so that drug development, filing of submissions and maintenance of product compliance, are undertaken in a timely manner, consistent with applicable Federal and Provincial Regulations.

ROLES AND RESPONSIBILITIES:

• Managing and leading the team on New Product Registrations, Labeling and Post approval submissions with Hea...