Qualifications Bachelors Degree in Pharmacy/Diploma in Pharmacy and Registration with the South African Pharmacy Council Experience 5 years experience in Regulatory Affairs, preferably in human medicines, including complementary medicines and medical devices for end-to-end regulatory activities. Good Manufacturing Practices (GMP) Pharmaceutical production experience or exposure to supplement regulatory knowledge. Core competencies Experience in use of CTD software builder and compilation of eCTD dossier applications. IT skills including Microsoft Office Ability to prioritise and work to tight deadlines Systems and operations analysis Ability to cope with a high degree of complexity and change Cross Functional skills: Ability to network, liaise and negotiate with others Ability to set standards and objectives and monitor progress Complex problem solving and decision-making skill Must demonstrate responsibility, excellence and collaboration and align with Company values
