(RA): Submit new dossiers for health products to authorities in South Africa and other markets (Namibia, Botswana material in compliance with legislation; submit to authorities as needed. Renew all registrations according assist with GMP in-house training. Act as an authorized representative for medical devices. B. Pharm
(RA): Submit new dossiers for health products to authorities in South Africa and other markets (Namibia, Botswana material in compliance with legislation; submit to authorities as needed. Renew all registrations according assist with GMP in-house training. Act as an authorized representative for medical devices. B. Pharm
of Course Development Software, Instructional Authoring Software, Instructional Education Models and Web
nted communicator and motivator with natural authority, a confident manner, and a highly performance-oriented
Process and submit relevant regulatory returns to authorities (SARS (VAT201, EMP201, EMP501, IRP6 etc.), UIF
Talented communicator and motivator with natural authority, a confident manner, and a highly performance-oriented
Submission of Relevant Regulatory Returns with Authorities (SARS (VAT201, EMP201, EMP501, IRP6 etc), UIF
Submission of Relevant Regulatory Returns with Authorities (SARS (VAT201, EMP201, EMP501, IRP6 etc), UIF
which we will contact you directly for your authorization to proceed with your application. Should you
reports to the GM, stakeholders, and regulatory authorities as required. Operational Finance Management: