New Openings at South African Health Products Regulatory Authority

• 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.
• Valid driver’s licence.

Deadline:21st November,2025

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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.

Deadline:21st November,2025

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• Review and verify all licence applications, Check all licence applications for completeness, correctness, and compliance, Reconcile and prepare reports, Imports and exports reconciliations, Follow up on defaulters, Follow up on non-renewals and non-returns, Process and update information on the database relating to: (Inspections and communicate non-compliances to Radiation Scientists, Source exchanges, Imports and exports), Process information related to radiation over-exposure on the database....

Qualification :

• Matric certificate and a BSc (Physics or Medical Physics) or a B. Rad. (Diagnostic/Nuclear Medicine/Radiotherapy) qualification.

Closing Date: Monday, 01 December 2025