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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Inspect pharmaceutical manufacturing sites for compliance with Good Manufacturing Practices as accepted by SAHPRA. Assess and evaluate GMP inspection reports of other regulatory authorities on international pharmaceutical manufacturing sites where medicines for exportation to South Africa are manufactured. Perform pre- and post-registration inspections on information submitted in a medicine application dossier.
Qualification :
Matric certificate and appropriate four-year Bachelor of Pharmacy degree and registration as a Pharmacist with the South African Pharmacy Council (SAPC) at NQF level 8 as recognised by SAQA or Honours degree in Chemistry/Engineering/Biochemistry/Biology/Microbiology or equivalent related qualification at NQF level 8 as recognised by SAQA plus a minimum of five (5) of experience in relevant pharmaceutical regulatory or GMP environment.
A relevant Master’s qualification at NQF level 9 as recognised by SAQA will be an added advantage.
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