Join Somagen Diagnostics as a Quality and Regulatory Affairs Lead in Mississauga. Oversee regulatory compliance, quality management systems, and enhance operational capabilities in the healthcare sector. This managerial position focuses on setting strategic objectives for regulatory affairs and quality controls within Canada’s largest independent provider of diagnostic solutions.

Your leadership will be crucial in integrating a Quality Management System and achieving ISO certification while ensuring product compliance and safety. Collaborate effectively across functions to streamline processes and foster a culture of quality excellence. Key Responsibilities:
Manage regulatory records and compliance standards
Develop ISO-oriented Quality Management System




Support regulatory communications and market access strategies
Oversee quality metrics and continuous improvement initiatives
Lead and develop staff in regulatory and quality roles Requirements:
Background in medical device Regulatory Affairs and Quality
Familiarity with Health Canada Medical Devices Regulations
Experience in QMS development and ISO standards
Proven leadership and project management capabilities
Excellent communication and decision-making skills Lead quality and regulatory processes that enhance healthcare outcomes at Somagen.

📌 Quality And Regulatory Affairs Lead At Somagen Mississauga
🏢 Diploma Healthcare Group
📍 Mississauga