This role involves supporting Adcock Ingram's Regulatory Affairs team in managing electronic and paper-based regulatory documents to ensure compliance with SAHPRA, EMA, and ICH standards. Key responsibilities include maintaining regulatory systems, preparing eCTD submissions, tracking application statuses, and coordinating publishing tasks across projects. The ideal candidate has 3-5 years of experience in Regulatory Affairs or a Life Sciences/IT qualification with 2-3 years of relevant experience. Strong Microsoft Office (including PowerBI) and eCTD software skills are required.