The South African Health Products Regulatory Authority (SAHPRA), is the National Medicines Regulatory Authority established in terms of the Medicines and Related Substances Act, 1965, (Act No. 101 of 1965) as amended, to provide for the monitoring, evaluation, regulation, investigation, inspection, registration and control of medicines, scheduled substances,...
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Provide regulatory strategic direction and management of activities of the Biological Medicines Unit, including risk management and audit, Supporting the work of the SAHPRA and its Advisory Committees, Management of evaluation and assessment of registration and amendments of biological medicines, Development/Update of technical guidelines and maintenance of policy, managing risk and audit queries, Conduct consultation meetings, Lot Release of Vaccines........
Qualification :
Matric certificate and a Bachelor of Pharmacy degree and NQF level 8 as recognised by the South African Qualifications Authority (SAQA) and a Master’s degree in pharmacy at NQF level 9.
A post-graduate qualification in management would be advantageous.
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