INSPECTOR GMP (GOOD MANUFACTURING PRACTICES)

A 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. A relevant master’s degree in Pharmacy qualification at NQF level 9 as recognised by SAQA will be an added advantage. Must have a valid driver’s licence. Comprehensive and sound knowledge of all relevant legislations, protocols, regulations, and guidelines about the Medicines and Related Substances Act 101 of 1965. Good verbal and numerical reasoning skills to allow analysis and interpretation of written and numerical data. Good communication skills (verbal, written, conflict management, and resolution). Resilience. Delivery of service objectives with professional excellence and efficiency. Ability to make effective decisions by using evidence Ability to work unsupervised for long periods. Ability to work within a team environment. Good planning and organisational skills. Ability to meet tight deadlines and manage multiple, often competing priorities.

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. *Perform a once-off evaluation on information submitted by HCR (Applicants). *Work closely with other inspection teams, SAHPRA departments, and external regulators to ensure inspection activities are planned and communicated effectively.

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