Regulatory Affairs (RA): Submit new dossiers for health products to authorities in South Africa and other markets research organizations for data generation for new product registrations or variations. Maintain dossiers review and quality management system for Act 101 products. Integrate ISO 13485 medical devices into the change controls. Conduct annual product quality reviews for Act 101 products. Review ongoing stability reports findings. Assist with QA batch release of Act 101 products in the absence of QA Manager and RP/Deputy RP
Regulatory Affairs (RA): Submit new dossiers for health products to authorities in South Africa and other markets research organizations for data generation for new product registrations or variations. Maintain dossiers review and quality management system for Act 101 products. Integrate ISO 13485 medical devices into the change controls. Conduct annual product quality reviews for Act 101 products. Review ongoing stability reports findings. Assist with QA batch release of Act 101 products in the absence of QA Manager and RP/Deputy RP
customer Technical team
library and manage incoming raw material and final products. BSc Food Science/Dip Food Technology or similar Final product against master sample Conduct sensory and chemical analysis Develop COA & Product Specification Capturing of QC results on internal system Filing of production sheets QC incoming raw materials Test against of filing system, both hard copy and digital – production sheets, supplier COA's, Kosher & Halaal Certificates