Highly driven and enthusiastic BSc Mathematics and MSc Bioengineering graduate, currently employed as a Regulatory Affairs Specialist for a medical devices manufacturer. Working with EU MDR Class III, FDA 510(k) haemostats and an advanced wound care range, primarily within the NPD team, assisting project teams with product realisation in line with global regulations and guidelines. Also taking regulatory lead within project teams on global device registrations and change controls for manufacturing and materials changes, interacting with customers, importers, distributors and authorised representatives to maintain global regulatory compliance for existing products in the post-market phase.