new agricultural products from inception to registration, including commercialisation and post launch Formulating and assessing trial reports to registration application standards. Working with internal
new agricultural products from inception to registration, including commercialisation and post launch Formulating and assessing trial reports to registration application standards. Working with internal
Responsibilities: Registration planning and business support Implement a registration plan and provide timely submission and approvals in line with the registration business plan. Timeous, comprehensive, and accurate accurate feedback to cross- functional teams. Registration plan Implemented and aligned with international compilation and dispatch: Complete due diligence of registration dossiers/ documents. Obtain relevant information Health Authorities regarding submissions, product registration or maintenance throughout the lifecycle of the
and registration of complementary medicines and other human medicines. Prepare the registration applications Ensure the maintenance and/or update of existing registrations in accordance with the relevant legislation
and legislation for drug development, product registration, line extension and license maintenance. Proven experience at a health authority. Implement a registration plan and provide business support. Provide regular timely submission and approvals in line with the registration business plan. Timeous, comprehensive, and accurate accurate feedback to cross- functional teams. Registration plan Implemented and aligned with international compilation and dispatch: Complete due diligence of registration dossiers/ documents. Obtain relevant information
and legislation for drug development, product registration, line extension and license maintenance. Proven experience at a health authority. Implement a registration plan and provide business support. Provide regular timely submission and approvals in line with the registration business plan. Timeous, comprehensive, and accurate accurate feedback to cross- functional teams. Registration plan Implemented and aligned with international compilation and dispatch: Complete due diligence of registration dossiers/ documents. Obtain relevant information
strategies, processes, and plans in support of new registrations and post-approval submissions. To ensure regulatory countries to enable efficient and effective registration of medicinal products consistent with the supported distributors, if applicable, on the progress of registration submission and approval activities, and ensure Knowledge and Skills required Experience in registration of products and regulatory knowledge of South
field.
related field. Professional certification or registration in SHEQ-related disciplines (e.g., SHEQ management
knowledge of the various territories where the registration process is required. Effectively managing, auditing