RegulatoryAffairsAnalyst

Welcome to Haleon. We’re a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we’ve grown, evolved and are now entering an exciting new chapter – one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands – including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® – lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it’s time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose – to deliver better everyday health with humanity – at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture. As a **Regulatory Affairs Analyst** , you will play a key role in ensuring that products across the LATAM Export Cluster markets comply with all applicable regulatory requirements while supporting commercial objectives. This role involves working closely with cross-functional stakeholders, maintaining regulatory systems, and contributing to regulatory strategies to enable efficient and compliant product launches and lifecycle management. **Key Responsibilities** * Support regulatory activities to ensure products (medicines, medical devices, cosmetics, and nutritional supplements) meet all compliance requirements across assigned markets. * Review and approve promotional materials in line with corporate policies and current regulatory legislation. * Maintain and update regulatory information in systems such as SAP and Veeva Regulatory with high business impact. * Support the preparation and submission of regulatory dossiers, applications, and documentation for new product launches and lifecycle management. * Monitor and assess regulatory changes, ensuring timely adaptation and communication of risk