Regulatory and Quality Specialist Role

Support quality systems at Vitaliti Technologies as a Regulatory and Quality Specialist. This role combines ISO expertise with hands-on collaboration in medical device settings.
Vitaliti Technologies in Kitchener, Ontario, seeks a detail-oriented Regulatory and Quality Specialist to enhance its quality processes and regulatory compliance. Ideal candidates will have over five years of experience in maintaining Quality Management Systems, particularly within ISO-controlled medical environments. Your role is to work cross-functionally, ensuring that documentation is precise and aligns with regulatory requirements.
Key Responsibilities:
• Communicate with regulatory agencies regarding trials and licensing approvals
• Oversee internal quality operations, such as inspections and product releases
• Ensure compliance of QMS documentation with relevant standards
• Help develop and improve standards and workflows in quality management
• Identify documentation gaps and manage...