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
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
the Occupational Health and Safety (OHS) Act, Road Transport Act, Governance Codes (Combined Code) of practice coaching on OHS Act . To ensure compliance with the OHS Act 85 of 1993 and COID Act. Accountable to providing compliance to legal provisions e.g., OHS Act, Environmental Act, and limited exposures. To be accountable follow safe working procedures in line with OHS Act, as well as customer requirements. 2.Administration legislation & procedure (OSHAct 93 of 1993, COID Act, etc.) and governance knowledge. Sound knowledge
the Occupational Health and Safety (OHS) Act, Road Transport Act, Governance Codes (Combined Code) of practice coaching on OHS Act . To ensure compliance with the OHS Act 85 of 1993 and COID Act. Accountable to providing compliance to legal provisions e.g., OHS Act, Environmental Act, and limited exposures. To be accountable follow safe working procedures in line with OHS Act, as well as customer requirements. 2.Administration legislation & procedure (OSHAct 93 of 1993, COID Act, etc.) and governance knowledge. Sound knowledge
sites and to ensure compliance with OHS and NEMA act. Responsible for all Risk related items on site and
sites and to ensure compliance with OHS and NEMA act. Responsible for all Risk related items on site and
Substances Control Act 101 of 1965, as amended and South African Pharmacy Act (Act 53 of 1974), and other
applicable), Medicines and Related Substances Control Act and South African Pharmacy Council, ensuring timeous guidelines Maintain current knowledge of relevant Acts, Regulations and Guidelines pertaining to the pharmaceutical
life-cycle maintenance. Knowledge of new and emerging Acts, Regulations and Guidelines pertaining to the pharmaceutical
life-cycle maintenance. Knowledge of new and emerging Acts, Regulations and Guidelines pertaining to the pharmaceutical