environment
following Acts and Tracing Tools: Knowledge of internal audit and client system National Credit Act Debt Collectors Collectors Act FICA Magistrate's and High Court Act, Rules and Procedures Municipal debt control and and by-laws Municipal system Act CPA Companies Act Prescription Act Experian, XDS, Traceps, Company searches
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following Acts and Tracing Tools: Knowledge of internal audit and client system National Credit Act Debt Collectors Collectors Act FICA Magistrate's and High Court Act, Rules and Procedures Municipal debt control and and by-laws Municipal system Act CPA Companies Act Prescription Act Experian, XDS, Traceps, Company searches
Purpose of the Job/KPAs Ensure compliance with the FIC Act by the Financial Institutions. Deal with referrals frameworks. Enforce and monitor compliance with the FIC Act by the financial institutions and conduct inspections of financial sector laws, FIC Act and the Financial Sector Regulation Act is essential. Good report writing
Purpose of the Job/KPAs Ensure compliance with the FIC Act by the Financial Institutions. Deal with referrals frameworks. Enforce and monitor compliance with the FIC Act by the financial institutions and conduct inspections of financial sector laws, FIC Act and the Financial Sector Regulation Act is essential. Good report writing
artwork review and quality management system for Act 101 products. Integrate ISO 13485 medical devices controls. Conduct annual product quality reviews for Act 101 products. Review ongoing stability reports, update (RP) of findings. Assist with QA batch release of Act 101 products in the absence of QA Manager and RP/Deputy licenses, and assist with GMP in-house training. Act as an authorized representative for medical devices products registered under Act 36 of 1947 would be an advantage. Experience with QMS (Act 101), change control
Equity Act, Skills Development Act, Labour Relations Act, and Basic Conditions of Employment Act. Facilitate Equity Act, Skills Development Act, Labour Relations Act, Basic Conditions of Employment Act, and other
Equity Act, Skills Development Act, Labour Relations Act, and Basic Conditions of Employment Act. Facilitate Equity Act, Skills Development Act, Labour Relations Act, Basic Conditions of Employment Act, and other
artwork review and quality management system for Act 101 products. Integrate ISO 13485 medical devices controls. Conduct annual product quality reviews for Act 101 products. Review ongoing stability reports, update (RP) of findings. Assist with QA batch release of Act 101 products in the absence of QA Manager and RP/Deputy licenses, and assist with GMP in-house training. Act as an authorized representative for medical devices products registered under Act 36 of 1947 would be an advantage. Experience with QMS (Act 101), change control