Elevate quality standards as a Quality Assurance Manager in Regulatory Affairs for medical devices. Lead QA activities and drive compliance in a rapid-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.#J-18808-Ljbffr

📌 Quality Assurance Manager In Medical Devices (Winnipeg)
🏢 Jobtailor
📍 Winnipeg