Requirements:
- Grade 12
- B.Pharm Degree
- 2 to 3 years' in the pharmaceutical manufacturing environment with QMS experience

Responsibilities:
- Ensure compliance of production, packaging and testing documentation to MCC, cGMP and Pharmacy Council requirements
- Audit completed batch manufacturing and packaging documentation
- Verification of bulk QC reports
- Review finished product release reports from the QC labs
- Ensure that the necessary in-process checks and controls during manufacturing and packaging are recorded
- Address and investigate deviations identified during batch documentation reviews and propose CAPA where necessary
- Release all batches of finished products on the system
- Maintain status of all batches of finished products on the system
- Verify correct manufacture and expiry dates of the products on the system prior to release