I bring a strong, multidisciplinary professional background that blends medical device labeling expertise, quality systems knowledge, and emerging AI and data capabilities. In my role as a Labeling Specialist, I have developed a deep understanding of regulatory requirements, including EU MDR and global market standards, ensuring that product labeling is accurate, compliant, and aligned with patient safety requirements. I am highly skilled in document control, change management, and cross-functional collaboration, with the ability to translate complex technical and regulatory information into clear, actionable deliverables. In parallel, my work in AI data annotation and quality evaluation reflects a forward-thinking mindset, strong analytical thinking, attention to detail, and the ability to critically assess outputs for accuracy and consistency. I combine analytical rigor with practical execution, allowing me to perform effectively in both highly controlled quality environments and evolving, technology-driven spaces.

To make contact, please e-mail me at [email protected].