Noxolo Magubane, Sr. Global Regulatory Affairs Specialist

  • Posted on Oct 31, 2018 at 17:33

Noxolo joined WCG in 2014 and she is currently working as the Sr. Global Regulatory Affairs Specialist where she is part of the Global Regulatory Affairs team and supports the registration of medical devices and drug products primarily in Africa.  Noxolo has over 7 years of experience in Regulatory Affairs field particularly in the registration of medical devices, biological and pharmaceutical products across the African region.   She holds a Post-Graduate Diploma in Pharmaceutical Medicine from Stellenbosch University and a Bachelor of Science degree in Biochemistry and Microbiology from the University of Kwa-Zulu Natal.

She began her career at Quintiles as a Clinical Research Apprentice.   In 2012, she joined Sanofi Pasteur as a Medical and Regulatory Affairs Associate, the main responsibilities for that role included drug safety and pharmacovigilance and various Regulatory Affairs activities such as clinical trial registrations, product registrations and submission of post-approval amendments and label updates in South Africa and various SADC countries.  She is an active member of the Southern Africa Pharmaceutical Regulatory Affairs Association (SAPRAA), Regulatory Affairs Professionals Society (RAPS) and the Organization for Professionals in Regulatory Affairs (TOPRA).  Noxolo has a publication in the TOPRA International Journal for Professionals in Regulatory Affairs (Regulatory Rapporteur).