As a Medical Device Guru at Greenlight Guru, I help medical device companies achieve and maintain regulatory compliance and quality excellence. I leverage my cross-functional and valuable team player skills to provide guidance, support, and training on the best practices of quality management systems, design control, and change control for Class I and II medical devices.Previously, I was a Quality Engineer at Handicare Stairlifts UK, where I implemented a robust quality management system that met the ISO 13485 and FDA CFR 820 requirements. I also performed internal audits, investigated complaints, reported MDRs, and facilitated CAPA progression. My passion for improving the quality of lives stems from my education background in biochemistry and cancer sciences, where I gained a strong foundation in molecular biology, cell signaling, and oncology. I hold a Master of Research degree from the University of Birmingham and a Bachelor of Science degree from the University of Wolverhampton, both with honors.