Specialist 2 - Regulatory Affairs (Medical Device Exp)

JobDiva ID: 25-30890 Duration: 10 months contract Job Description: Regulatory Associate or Regulatory Specialist (depending on the skill/experience level of the candidate) Responsibilities: Support/manage medical device regulatory change assessments and regulatory submissions to Health Canada, system updates, managing documentation and other duties. Previous regulatory affairs experience is required, specifically with experience with Medical devices Experience: Include the level of experience that is expected from the candidate. Skillsets: Excellent communication and comprehension of the English language, Proficiency with Microsoft Excel and general computer skills, Multi-tasking with attention to detail Education: Bachelor’s Degree