Job Description

Full job descriptionThe Focus Group Sandton, South Africa 10 February 2026 Mid 65000 - 80000 Full Time Cost to Company 5 years - 8 years Skills Dispensing (Medical) Management Medical Medical Assistance Medical Nutrition Therapy Medical Sales Medication Administration Medication Management Pharmaceutical Teamwork Industries Healthcare Medical Pharmaceutical Job DescriptionSUMMARYThe Regulatory Affairs Pharmacist will compile, submit and track the regulatory submissions for the clients product portfolio and ensure compliance with the related Acts and guidelines of each territory and includes registration, pre-approval and post-approval activities. Monitoring and reviewing project progress on an ongoing basis. Ensuring the timely completion of responsibilities and activities in line with the business goals.RESPONSIBILITIESEvaluation, compilation and submission of accurate new product applications and post registration dossier amendments to SAHPRA and African Regulatory Authorities, in accordance with established and current formats and requirements.Maintenance of registration dossiers in compliance with regulatory requirements, including submission of renewals in South Africa and across Africa.Submission of labelling updates in line with the timelines and country specific requirements.Evaluation of artwork changes and initiation of artwork.Review of promotional material in accordance with relevant Promotional and Marketing Codes.Liaising with SAHPRA & the Regulatory Authorities in Africa (English speaking).To act as Deputy Responsible Pharmacist in the absence of the Responsible Pharmacist when required.EDUCATION AND EXPERIENCEB. Pharm DegreePharmacist registered with the South African Pharmacy Council.5 years’ experience in a South African pharmaceutical regulatory affairs environmentAdvantage: Biological product submissions across the African regionPrevious Animal Health industry experience would be an advantageTECHNICAL AND BEHAVIORAL SKILLS REQUIREMENTS