In my role on the Regulatory Affairs Team, I lead the preparation of regulatory applications to gain market clearance for orthopaedic implants and accessories across various jurisdictions, including the US FDA, regions following EU MDR requirements, Mexico etc. My responsibilities extend to creating medical device labelling, managing regulatory documentation, coordinating MDSAP audit responses, and providing regulatory guidance at all organisational levels. Additionally, I assist with an array of pre- and post-market initiatives, and providing regulatory guidance to all relevant departments.

Member of the Materials Engineering Team. This experience has greatly enhanced my technical expertise as well as my soft skills. My key responsibilities include literature research, design of experiments, conducting laboratory testing, technical review and providing detailed technical reports for failure analysis and regulatory compliance. I also manage supplier development/relationships while maintaining effective stakeholder communication across all levels for the above projects.

Tutoring in Primary school to year 12 level mathematics. It enhanced my ability to convert information into a digestible format for diverse audiences.

Designed and prototyped a limb capture device aimed at assisting with lower limb prosthetic fitting, this experience greatly enhanced my leadership ability, CAD design, communication skills, and hands-on prototyping skills.

Contributed to research efforts focused on exploring lithium battery electrode materials. I gained practical knowledge and skills in various characterization techniques, including SEM and Raman Spectroscopy.