needed to drive performance in their respective departments. Robust mitigation plans in place to engage. , LRMP Labelling and Artwork Management Robust Health Authority interactions To track and manage all Marketing Authorization Applications to the SA Health Authority according to SA HA guidelines and GRP business priorities. License maintenance: Ensure all post-approval product maintenance activities including technical changes to the label or the packs, PBRERs, and post approval commitments are submitted and approved
interpreting, presenting and discussing this data with health professionals during face-to-face interactions patients ‘needs; Collaborating with the Medical Department to plan and execute educational/scientific activities Administrative Support Staff Pharmacists Related Health Care Professionals e.g. Nurses Radiology Directors
interpreting, presenting and discussing this data with health professionals during face-to-face interactions patients ‘needs; Collaborating with the Medical Department to plan and execute educational/scientific activities Administrative Support Staff Pharmacists Related Health Care Professionals e.g. Nurses Radiology Directors
registration of medicines with the South African Health Products Regulatory Authority and the maintenance Responsible and accountable to the South African Health Products Regulatory Authority and the South African provide insight into RA activities and report on department progress. Form part of the global Senior Leadership
registration of medicines with the South African Health Products Regulatory Authority and the maintenance Responsible and accountable to the South African Health Products Regulatory Authority and the South African provide insight into RA activities and report on department progress. Form part of the global Senior Leadership
Commerce – Procurement and/or Supply Chain Management Post Grad Degree will be advantageous Degree plus 5 years' management level Sound understanding of Safety, Health and Environment Ensure team compliance with the
processes, and plans in support of new registrations and post-approval submissions. To ensure regulatory input strategies are defined and executed and Board of Health requirements are met, ensuring a submission ready
order forecasts to Responsible Pharmacist to secure post importation testing readiness of labs Warehouse
order forecasts to Responsible Pharmacist to secure post importation testing readiness of labs Warehouse
Qualifying Requirements are: CA(SA) Minimum 5 years post articles experience Overall strong IFRS knowledge