Requirements:
- Grade 12
- B.Pharm degree
- Registered with the SAPC
- Minimum 2 to 3 years' experience in a pharmaceutical manufacturing environment
- Minimum 2 to 3 years' QA experience
- cGMP skills

Responsibilities:
- Compile, review and approve QMS SOP's to ensure compliance to the GMP guidelines
- Train relevant staff on SOP's
- Review change controls, deviations and assessing the impact of the change and non-conformance on quality procedures
- Review investigations arising from customer complaints
- Identify and implement preventative actions
- Perform internal audits as per schedule, compile reports and follow up on CAPA
- Participate in risk assessments on QMS and departmental processes
- Participate in Quality Management Reviews to identify trends in QMS processes and implement CAPA's
- Initiate, review and finalise technical agreements with all the company contractors, raw material and packaging suppliers
- Implement the recall process timeously
- Review master batch documents for compliance
- Ensure technical reviews on dossiers are performed
- Monitor and assess any OOS and OOT from the stability reports