Job Purpose: To assist and maintain aspects of the Quality Management System, adhering to SA GMP requirements and those of the Office of Global Quality. To assist with Pharmaceutical Quality System elements (Quality Complaints Investigations, PQR’s, Quality Risk Management) To review and authorize Non-conformance Reports, Change Controls and complete Master Batch Documentation Review.

Main Duties and Responsibilities are: Ensure that the QA Database is accurately maintained. Generate and review Standard Operating Procedures. To provide support to the business by timeous review of products for release. Product Release and Supply: to ensure timeous QA release of stock from warehouse; to assess laboratory requirements for new product analysis; to assist in reviewing the monthly Schedule of Open Orders to set-up laboratories in advance of delivery of product; to compile the Monthly Metrics re...