System to be SAHPRA inspection-ready at all times and assume all the responsibilities of the Responsible are kept of all product batches released to market. Quality Management Processes: Manage all final product place to ensure high quality products. Ensure that all manufacturers, laboratories, packers, warehouses in place to maintain the positive GMP status of all sites. Also oversee that global audits are performed that Quality Technical Agreements are in place for all sites utilised for products, and that these are maintained
System to be SAHPRA inspection-ready at all times and assume all the responsibilities of the Responsible are kept of all product batches released to market. Quality Management Processes: Manage all final product place to ensure high quality products. Ensure that all manufacturers, laboratories, packers, warehouses in place to maintain the positive GMP status of all sites. Also oversee that global audits are performed that Quality Technical Agreements are in place for all sites utilised for products, and that these are maintained
Facilitate training and perform all training required by laboratories. Maintain all training matrices and training training records of all laboratory staff. Conduct training and co-ordinate training with external providers line with current and future needs Update and track all learning and development initiatives, keep track identify barriers to learning Manage all training administration and ensure all compliance and audit requirements
Facilitate training and perform all training required by laboratories. Maintain all training matrices and training training records of all laboratory staff. Conduct training and co-ordinate training with external providers line with current and future needs Update and track all learning and development initiatives, keep track identify barriers to learning Manage all training administration and ensure all compliance and audit requirements
to stakeholders and in the correct format. Manage all Final product manufacturers, Final Release Laboratories quality systems to ensure quality products Ensure that all Manufacturers, Laboratories, Warehouses and Distributors in place to maintain the positive GMP status of all Manufacturers, Laboratories, Warehouses and Distributors that Quality/Technical agreements are in place for all our products Manage and facilitate artwork projects Quality Systems and ensure that the SOP's are guiding all personnel in a clear and understandable manner Support
to stakeholders and in the correct format. Manage all Final product manufacturers, Final Release Laboratories quality systems to ensure quality products Ensure that all Manufacturers, Laboratories, Warehouses and Distributors in place to maintain the positive GMP status of all Manufacturers, Laboratories, Warehouses and Distributors that Quality/Technical agreements are in place for all our products Manage and facilitate artwork projects Quality Systems and ensure that the SOP's are guiding all personnel in a clear and understandable manner Support
tender applications. Responsibilities: Maintenance of all Internal Price files on Oracle. Assist with Price necessary filling system on a monthly basis. Coordinate all Single Exit Price related functions. Check the Department of Health website for published tenders. Prepare all relevant documentation for tender submissions to
compliance with all the provisions of the Act 101 of 1965; Pharmacy Act, Act 53 of 1973 and all regulations (RP) with all tasks where required. Deputize the Responsible Pharmacist (RP) by performing all RP duties
compliance with all the provisions of the Act 101 of 1965; Pharmacy Act, Act 53 of 1973 and all regulations (RP) with all tasks where required. Deputize the Responsible Pharmacist (RP) by performing all RP duties
within oncology practices. Maintaining a data-base of all targeted clients. Liaising with the Sales Manager Ability to develop business relationships with all stakeholders in oncology/hematology practices for