Seeking an Expert in Regulatory Affairs to ensure excellence in medical device compliance. Lead the coordination of regulatory submissions to enhance surgical outcomes within the Canadian healthcare sector. In this specialized role, you will prepare submissions while ensuring conformity with Health Canada regulations. Collaborate with R&D;, Quality, and Clinical teams to streamline documentation processes and improve compliance tracking. Your attention to detail will support internal audits and help uphold the high standards necessary in medical device registration. Key Responsibilities: • Prepare regulatory submissions and document packages • Coordinate materials for annual registrations • Recommend compliance changes to documentation • Prepare for internal audits and inspections • Stay updated on regulatory changes Requirements: • Bachelor's degree in relevant discipline • 2+ years regulatory experience in medical devices • Robust knowledge of Canadian regulatory standards • Excellent organizational and communication skills • Ability to work independently and manage documentation Enhance your career while making significant contributions to medical compliance and innovation.
Apply on Kit Job: kitjob.ca/job/2fsp18
📌 Expert Regulatory Affairs Lead for Canadian Medical Devices (Anchor Point)
🏢 VB Spine
📍 Anchor Point
Reply to this offer
Impress this employer describing Your skills and abilities, fill out the form below and leave Your personal touch in the presentation letter.