Reference: HC003465-Nomfu-1 Job Summary/Purpose Regulatory: Responsible to ensure that regulatory submissions and compliance are executed for all products in South Africa. Develop and communicate with head office on the regulatory strategy and life cycle management of all products in South Africa. R
Education/Degree
B.Pharm Degree
Registered with The South African Pharmacy Council
Recommended experience needed:
· 2-3 Years experience in compilation and submission of Act 101 dossiers.
· Knowledge of Act 36 dossier submissio
Reference: HC003465-Nomfu-1 Job Summary/Purpose Regulatory: Responsible to ensure that regulatory submissions and compliance are executed for all products in South Africa. Develop and communicate with head office on the regulatory strategy and life cycle management of all products in South Africa. R
change documentation. Perform testing and quality assurance on system changes in the test environment environment. Document the testing and quality assurance results of the changes in the test environment. Perform Perform testing and quality assurance on system changes in the production environment. Ensure system codes
Minimum 8 years of hands-on experience in Quality Assurance, with a strong foundation in SDLC and STLC
discipline. Minimum of 3-5 years of experience in quality assurance, process improvement, or a related field.
discipline. Minimum of 3-5 years of experience in quality assurance, process improvement, or a related field.
Responsible for the Education and Training Quality Assurance and administrative performance of the department;
business processes and operations. Testing and Quality Assurance: Develop test plans and test cases to validate