Company:
South African Health Products Regulatory Authority
Industry: Healthcare / Medical
Deadline: Nov 7, 2025
Job Type: Full Time
Experience: 3 years
Location: South Africa
Province:
Field: Administration / Secretarial
REQUIREMENTS:
- Matric certificate and an appropriate 3-year Bachelor of Science Degree at NQF
- level 7 as recognised by SAQA (Appropriate 4-year degree in Chemistry/Pharmacology or Bachelor of
- Pharmacy will be an advantage), and registration with a statutory council if applicable. Three (3) years of relevant regulatory experience. Experience in product review or assessments will be an added advantage.
COMPETENCIES:
- Knowledge and good understanding: Theoretical knowledge of technical aspects for the evaluation of medicines across all fields, namely: Medicines and Related Substances Act (101 of 1965). Safety and efficacy. Quality and bioequivalence. Naming and scheduling. Good
- Manufacturing Practice. Knowledge of the regulatory environment. Good Clinical Practice.
- Pharmacovigilance.
Skills:
- Comfort working with computers and computer software packages.
- Displays a strong
academic background.
- Good and effective communication skills (written and verbal).
- Planning and coordination skills.
- Conflict management.
- Critical thinking and problem-solving skills.
Self Management.
- Attributes:
- Able to remain self-motivated with the ability to work independently.
- Positive attitude.
- Team player.
- Ability to work precisely and efficiently.
- Ethical behaviour and adherence
- to the SAHPRA Code of Conduct. Flexible. Deadline driven. Honest. Ability to prioritise and display
- excellent time management skills. Ability to work under pressure. Ability to tolerate stress.
- Responsiveness. Relationship management.
DUTIES:
- Technical screening of medicines applications:
- Assess each module of the application
- against the relevant technical screening form to ensure they are appropriate in terms of format and
- content as defined by the relevant guidelines.
- Generate a validation report
