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

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.

📌 Quality Assurance Manager in Medical Devices (Burnaby)
🏢 Jobtailor
📍 Burnaby