About South African Health Products Regulatory Authority
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, ... read moreregistration and control of medicines, scheduled substances, clinical trials and medical devices, and related matters in the public interest.
EXECUTIVE MANAGER: HUMAN RESOURCES MANAGEMENT
South African Health Products Regulatory Authority Jobs in South Africa
SALARY: R309 253.00 – R328 223.00 PER ANNUM (TOTAL COST TO COMPANY)
Ref No.: SAHPRA 64 of 2025/26
CENTRE: Pretoria
REQUIREMENTS: Applicants must hold a Matric certificate and a three-ye
Qualification :
Matric certificate plus a BSc Hons Medical Physics
Professional registration with HPCSA
Valid driver’s licence is essential.
Required Skills
Self-
Qualification :
Minimum of two (2) years of administration experience. Must be computer literate
Required Skills
Administrative practices, record keeping, and report preparation.
Plan and perform inspections in accordance with the Hazardous Substances Act, related regulations and code of practice, Prepare formal reports of your finding/s during inspections,
Participate in
Reviewing a broad range of applications as a primary-, peer reviewer.
Conducts evidence-informed practice.
Makes or recommends regulatory decisions.
Qualification :
Matric certi
Evaluation and assessment of the quality, safety and efficacy of new applications for the registration of Biological Medicines,
Evaluation and assessment of applications for the amendment of the
Evaluate and generate evaluation report(s) for registration applications (Generics & New Chemical Entities) in compliance with required template and adopted regulatory /scientific standards (SA
Evaluation and assessment of the quality, safety and efficacy of new applications for the registration Biological Medicines,
Evaluation and assessment of applications for the amendment of the qua
Develop strategy, annual performance plan, operational plans, and budget for the Medical Device and Radiation Control Programme, aligned with organisational needs and optimal resource utilisation,
Manage the operations of the Biological Medicines Unit concerning the processes, inputs, targets, outputs, and resourcing requirements to ensure effective operation within the unit,
Manage the de
Operational Management Ensure compliance with the provisions of the Medicine and Related Substances Act 101 of 1965 as amended, through the implementation of the strategies for preventing, detectin
Inspect different disciplines of pharmaceutical manufacturing, importing or exporting sites such as import/export/applicant and non-sterile manufacturing for compliance with Good Manufacturing Prac
Responsible for the accurate and timeous assessment of safety documents received, and performance as per the defined processes. Preparing comprehensive reports for various purposes (e.g., regulator
Develop and monitor the CEO office operational plans aligned to strategic goals, boosting productivity and efficiency. Oversee project execution from management and stakeholder meetings, preparing
Grade 1: Four-year Bachelor of Pharmacy degree NQF or Honours degree in Chemistry or equivalent related qualification at NQF level 8 as recognised by SAQA, plus a minimum of five (5) years of exper
Ensure that all imported health products possess applicable SAHPRA authorisations, e.g., licence, product authorisation, certificate, or permit, before release into the Republic. Stop non-compliant
Strategic Planning & Technology Leadership: Develop, secure approval, and implement strategic technology plans aligned with business goals and digital transformation objectives. Define and main
Purpose of the role
The purpose of the role is to co-ordinate the allocation of applications to evaluators to ensure that applications are compliant with the Medicines and Related Substances Act
