Requirements:
- Grade 12
- B.Pharm degree
- 3 to 5 years' in the pharmaceutical manufacturing environment, with QMS experience
- Knowledge of Quality Assurance, relevant current Medicine Regulatory Authority guidelines
- Computer literate

Responsibilities:
- Maintain and improve the Quality Management System
- Perform internal audits of all departments for compliance with cGMP and regulatory requirements
- Maintain an effective Change Control reporting system and evaluate proposed changes
- Maintain an effective Deviation reporting system and evaluate deviations for effective root cause analysis
- Review site SOP's for compliance with local and international cGMP guidelines
- Investigate customer complaints and compile reports for closure. Track & trend status for CAPA and improvements
- Monitor and track CAPA as a result of audit findings, deviations, risk assessments and customer complaints
- Maintain accurate documentation systems
- Training staff on quality systems
- Prepare data for and participate in the Quality Management Review Meetings
- Assist with release with final products where required