I am an experienced engineer and researcher with over five years in the med-tech industry, currently serving as a Risk Manager. My expertise spans research and development in healthcare technology, including the conceptual design and experimental validation of medical prototypes. In my current role, I implement risk-based approaches to ensure compliance with international standards for medical devices. I am also focused on process improvement initiatives, aiming to optimize development and operational workflows for efficiency and quality. My work is dedicated towards developing risk management framework for devices and processes that prioritizes integration with quality assurance and regulatory compliance, thereby enhancing patient safety.