Assisting the regulatory manager in the compilation of new registration submissions, dossier updates, dossier maintenance and dossier conversions for ethical and veterinary pharmaceuticals, including NCE's, generics, line extensions and parallel registration submissions in accordance with SAHPRA's regulatory requirements.Comprehensive dossier reviews (ethical and veterinary) for new submissions, dossier updates, dossier maintenance and dossier conversion submissions in accordance with SAHPRA's regulatory requirements.Drafting, maintenance and updating of PI's, PIL's and Labels in accordance with SAHPRA's regulatory requirements.Compilation and review of new registration submissions, dossier updates, dossier maintenance and dossier conversions for veterinary products registerable with the Act 36 Authority.