About

• Bachelor's or master's degree in a scientific, technical, or related discipline. 2+ years of regulatory affairs experience in the medical devices industry. Postgraduate certification in a regulatory affairs program. Working knowledge of the Canadian regulatory environment and Health Canada regulations, policies, and guidance. Previous experience with Class II or III device submissions. Demonstrated ability to effectively manage multiple projects and priorities. Basic computer skills, including Microsoft Word, Excel, Teams, PowerPoint, and Adobe Acrobat. Excellent written and oral communication, technical writing, and editing skills. Advanced computer skills to support submissions, communication, and presentations (e.g., MS Word troubleshooting such as references, section building, tables of contents). Quick learner, self-motivated, and independent worker with moderate supervision. Works well in fast-paced, cross-functional team environments.