Elevate quality standards as a Quality Assurance Manager in Regulatory Affairs for medical devices. Lead QA activities and drive compliance in a fast-paced workplace.

In this leadership role, you will oversee daily Quality Assurance and Regulatory Affairs operations, ensuring they align with ISO 13485 requirements. With 5-10+ years of experience, you will coach a team, build cross-functional relationships, and establish KPIs for continuous improvement in quality metrics.

Key Responsibilities:
• Lead day-to-day QA and Regulatory Affairs activities
• Establish goals and track quality objectives
• Coach and develop QA/RA team members
• Ensure audit readiness across various functions
• Directly execute critical QA/RA work hands-on

Requirements:
• 5–10+ years in Quality Assurance leadership
• Experience in ISO 13485 environments
• Proven experience with audit management and CAPA systems
• Strong communication skills with stakeholders
• Background in engineering or science preferred

Drive the success of regulatory compliance and quality management in the medical device sector.
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📌 Quality Assurance Manager in Medical Devices (British Columbia)
🏢 Jobtailor
📍 British Columbia