Regulatory Affairs Analyst (15-month contract) PURPOSE Prepares labelling submissions and manages all aspects of labelling using conventional methods or NNCI's labeling system. Prepares submissions and obtains Health Authority approval for post-approval changes for marketed products and Clinical Trial Submissions for products in development. Prepares medical device submissions for new and existing devices, and performs related medical device activities, including maintenance of medical device licenses. Manages assigned projects. RELATIONSHIPS REPORTS TO:... ## Type: Permanent ## Location: Mississauga - Peel, Ontario, Canada