Become a Quality Management Specialist at Vitaliti Technologies Inc. in Kitchener, Ontario, focusing on regulatory compliance and process efficiency. This position demands strong attention to detail and independent working capabilities.
The role of Quality and Regulatory Specialist is tailored for those with 5+ years in regulated environments, especially in medical devices. You will work hand-in-hand with teams to ensure QMS documentation meets ISO standards and support audits. This hands-on position is essential for maintaining compliance while driving quality initiatives forward.
Key Responsibilities:
• Liaise with regulatory bodies for device licensing and clearance
• Oversee quality processes, including inspections and product releases
• Ensure documentation conforms to regulatory standards
• Assist in developing QMS standards and workflows
• Conduct gap analyses and manage documentation updates
Requirements:
• 5+ years in a regulated quality setting
•...