years' experience in Regulatory Affairs, preferably in human medicines Demonstrable experience across quality, time and cost standards Competencies: Experience in use of CTD software builder and compilation
advantageous Preferred experience: A minimum of 3 years within similar roles. 5 years' experience with the Pharmaceutical having worked within the Emerging Africa Markets. Experience working in a pharmaceutical industry and general knowledge of drug development and clinical research Experience in Scientific report writing would be advantageous organizing essential Ability to work under pressure. Experience working in a pharmaceutical industry and general
Plastician Extrusion-related (PSA). Minimum Working Experience: 5 Years of Supervision in the Plastics Technology