Posted:
10/5/2025, 5:44:52 PM
Location(s):
Alberton, Gauteng, South Africa ⋅ Gauteng, South Africa
Experience Level(s):
Mid Level ⋅ Senior
Field(s):
Legal & Compliance
1. Regulatory Affairs
- Prepare, submit, and maintain SAHPRA dossiers.
- Monitor regulatory changes and provide regulatory intelligence.
- Support in inspections and audits.
- Coordinate responses to authorities.
- Maintain a registration database.
2. Pharmacovigilance
- Collect, assess, and report adverse events.
- Maintain pharmacovigilance systems.
- Draft and maintain Risk Management Plans and PSUR’s.
- Responsible for pharmacovigilance audits (Self inspection, ALLISA audit and external audit).
- Communicate safety updates to stakeholders.
3. Quality & Compliance
- Ensure GxP compliance.
- Document control, deviation handling, CAPA.
- Provide training on regulatory/PV requirements.
- Collaborate with QA, production, and distribution teams.
- Bachelor of Pharmacy (BPharm) or equivalent.
- Registration with the South African Pharmacy Council.
- 3–5 years’ experience in regulatory affairs, QA, or pharmacovigilance.
- Strong knowledge of SAHPRA, ISO, WHO GxP/GVP, GMP/GDP standards and regulations.
Our Differences make our Performance
At Air Liquide, we are committed to build a diverse and inclusive workplace that embraces the diversity of our employees, our customers, patients, community stakeholders and cultures across the world.
We welcome and consider applications from all qualified applicants, regardless of their background. We strongly believe a diverse organization opens up opportunities for people to express their talent, both individually and collectively and it helps foster our ability to innovate by living our fundamentals, acting for our success and creating an engaging environment in a changing world.
Website: https://airgas.com/
Headquarter Location: Radnor, Pennsylvania, United States
Employee Count: 10001+
Year Founded: 1982
IPO Status: Delisted
Industries: Industrial ⋅ Medical ⋅ Retail