Oneaho Monyileote is a Regulatory Affairs and Quality Assurance Specialise with over 10 eight years of experience in in medical devices, in vitro diagnostics (IVDs), pharmaceuticals, and biotechnology sectors. Her expertise spans regulatory licensing as a Medicine Registration Officer at SAHPRA, quality management systems implementation, risk management, auditing and GxP. She is passionate about translating complex regulatory and quality requirements into practical, compliant solutions that support product safety, operational excellence, and continuous improvement within regulated healthcare environments.
