Minimum requirements for the role: Must have a relevant tertiary qualification SACNASP registration would be ideal Minimum 5 years experience in Act36/1947 regulatory management and product development Experience with GHS labelling requirements is essential Strong communication and public relations skills The successful candidate will be responsible for: Managing the regulatory function in South Africa. Preparing generic and biological dossiers, including tracking product registrations and approval timelines. Preparing label extensions and amendments. Managing technical data, samples, and residue studies. Liaising with appointed consultants. Liaising with global suppliers. Liaising with CropLife South Africa and participating in working groups. Liaising with Act 36/1947 and ensuring compliance with the latest guidelines. Managing MSDS, labels, and Trem cards. Providing regulatory support to the global stewardship function in risk management of registered products and implementing mitigation strategies to ensure compliance with Act 36/1947 requirements. Providing regulatory support to the commercial function. Providing regulatory support for South African registrations to regulatory personnel in other countries to ensure registration expansion. Representing the company at events. Please note that subsequent to the screening and shortlisting process, all further communication will be entered into only with the shortlisted candidates. If you do not receive any feedback from us within 2 weeks of applying, please consider your application unsuccessful.