Over the past decade, I have worked across academic and industrial environments— from research institutes in Portugal, the UK, and Germany, to start-ups and global medical device companies. My core expertise lies in regulatory affairs and quality management, with a focus on requirements engineering, risk-based verification and validation, documentation management, and compliance strategy. I have successfully guided numerous medical products to market by translating complex regulations into structured, actionable processes. Since 2016, I have complemented my medical device background with cross-industry experience, working in diverse product environments where I gained profound insight into product safety, system reliability, and regulatory strategy beyond the medical field. This broadened perspective enables me to bring cross-sector thinking to regulatory challenges and content planning. Since 2019, I have actively mentored young professionals and co-supervised master’s thesis in Germany.