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 standardsDevelop ISO-oriented Quality Management SystemSupport regulatory communications and market access strategiesOversee quality metrics and continuous improvement initiativesLead and develop staff in regulatory and quality rolesRequirements:Background in medical device Regulatory Affairs and QualityFamiliarity with Health Canada Medical Devices RegulationsExperience in QMS development and ISO standardsProven leadership and project management capabilitiesExcellent communication and decision-making skillsLead quality and regulatory processes that enhance healthcare outcomes at Somagen.

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