The South African Health Products Regulatory Authority (SAHPRA) is actively seeking professionals to join its team in key roles that support the regulation and oversight of health products, clinical trials, and medical devices across South Africa. If you are passionate about contributing to public health and safety, SAHPRA offers a range of career opportunities in Durban, Port Elizabeth, and Pretoria. Read on to learn more about the exciting positions currently available, the skills required, and how you can apply.
1. Border Medicines Control Technician – Durban & Port Elizabeth
Job Overview
SAHPRA is looking for two experienced Border Medicines Control Technicians to work at Durban Harbour and Port Elizabeth Harbour and Airport. The primary responsibility of this role is to monitor the compliance of imported health products, ensuring that only safe and regulated products enter the country.
Salary Range
R434,554.00 – R461,223.00 per annum (Total cost to company)
Requirements
- Education: Matric certificate and Advanced Certificate: Pharmacy Technical Support qualification.
- Experience: At least 2 years’ experience as a Pharmacy Technician or Post-Basic Pharmacist Assistant.
- Skills: Strong knowledge of the Medicines and Related Substances Act, regulatory protocols, communication, and decision-making skills. Proficiency in MS Office and the ability to work independently.
Key Responsibilities
- Ensure compliance of all imported health products at South African ports.
- Work closely with border control agencies and Port Health to ensure regulatory adherence.
- Monitor and report on compliance status, issuing corrective actions where necessary.
- Maintain records of import-related documents and create weekly reports.
How to Apply
Interested applicants must submit their applications through the SAHPRA website portal at SAHPRA Careers. The closing date for applications is 14 March 2025 at 16:00.
2. Call for Expression of Interest: Clinical Trials External Evaluators
SAHPRA is inviting experts to serve as External Evaluators for the evaluation of clinical trials, including safety and efficacy assessments. These evaluators play a crucial role in supporting SAHPRA’s work in regulating clinical trials and medicines in South Africa.
Salary Range
This role offers a flexible hybrid working model with competitive compensation.
Requirements
- Qualifications: MBChB, BPharm, or a Master’s in Health Sciences (preferable).
- Experience: Minimum 5 years in clinical research or medicine regulation.
- Skills: Deep knowledge of Good Clinical Practice (GCP), clinical trial legislation, safety data interpretation, and pharmacology.
Duties
- Review Serious Adverse Event (SAE) reports, progress reports, and study safety reports.
- Analyze clinical trial data and provide recommendations for regulatory decisions.
- Collaborate with multidisciplinary teams on clinical trials projects and advise on improvement measures for safety reporting systems.
How to Apply
To apply for the Clinical Trials External Evaluators position, submit your CV and supporting documents via SAHPRA External Evaluators Application Portal. The closing date is 13 March 2025 at 16:30.
Why Work with SAHPRA?
SAHPRA is South Africa’s key regulatory authority overseeing the safety and efficacy of health products, including medicines, medical devices, and clinical trials. Working with SAHPRA gives you the opportunity to make a tangible impact on public health by ensuring the safety of medicines and other health products used across the country.
As a part of the team, you will be involved in critical decision-making processes that shape public health policy and help safeguard the well-being of millions. The roles offered provide opportunities for professional development, with a focus on building expertise in the regulatory field.