Senior regulatory affairs pharmacists
Jordan HR Midrand
Qualifications
Bachelors Degree in Pharmacy/Diploma in Pharmacy and Registration with the South African Pharmacy Council
Experience- 5 years experience in Regulatory Affairs, preferably in human medicines, including complementary medicines and medical devices for end-to-end regulatory activities.
- Good Manufacturing Practices (GMP)
- Pharmaceutical production experience or exposure to supplement regulatory knowledge.
- Experience in use of CTD software builder and compilation of eCTD dossier applications.
- IT skills including Microsoft Office
- Ability to prioritise and work to tight deadlines
- Systems and operations analysis
- Ability to cope with a high degree of complexity and change
- Cross Functional skills: Ability to network, liaise and negotiate with others
- Ability to set standards and objectives and monitor progress
- Complex problem solving and decision-making skill
- Must demonstrate responsibility, excellence and collaboration and align with Company values
Jordan HRMidrand
Qualifications
• Bachelors degree in Pharmacy/Diploma in Pharmacy and Registration with the South African Pharmacy Council
Relevant experience
• Minimum of 5 years experience in Regulatory Affairs, preferably in human medicines
• Demonstrable...
CuriskaJohannesburg, 25 km from Midrand
Hiring: Regulatory Affairs Manager
Location: Midrand, South Africa
As a Regulatory Affairs Manager, you will oversee product registration and dossier maintenance in the SEA Cluster, ensuring compliance with regulations and pharmacovigilance...
Midrand
Overview
Hire Resolve’s client is actively seeking a Regulatory Affairs Manager to join their team in Midrand, Gauteng. As a Regulatory Affairs Manager, you will be responsible for ensuring a thorough and seamless product registration process...