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.
Hello. We’re Haleon. A new world-leading consumer health company. Shaped by all who join us. Together, we’re improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands – including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum – through a unique combination of deep human understanding and trusted science. What’s more, we’re achieving it in a company that we’re in control of. In an environment that we’re co-creating. And a culture that’s uniquely ours. Care to join us. It isn’t a question.
With category leading brands such as Sensodyne, Voltaren and Centrum, built on trusted science and human understanding, and combined with our passion, knowledge and expertise, we’re uniquely placed to do this and to grow a strong, successful business.
This is an exciting time to join us and help shape the future. It’s an opportunity to be part of something special.
About the role
The Regulatory Affairs Manager ensures compliant market access for diverse portfolios (medicines, devices, cosmetics, foods) by leading product registration, labeling, and claims aligned with commercial goals. They maintain ongoing compliance, manage health authority interactions, and oversee submissions and inspections. Serving as a key strategic partner, they collaborate cross-functionally with marketing, supply chain, and quality teams while coaching junior staff. Externally, they build strong relationships with regulators and industry bodies to facilitate approvals. Finally, they monitor regulatory trends, mitigate risks, and drive continuous improvement to support successful product launches and lifecycle management.
Key responsibilities
Product Lifecycle & Launch Management: Lead the end-to-end regulatory process for new product launches and lifecycle maintenance (NPD & Line Extensions), utilizing systems like Veeva Vault to prepare dossiers, secure registrations, and ensure compliant labeling and claims aligned with commercial plans.
Regulatory Strategy & Risk Mitigation: Develop robust regulatory strategies (e.g., RSD) and conduct gap analyses to identify risks early; proactively manage the impact of regulatory changes and propose solutions to ensure products are scientifically robust and legally compliant.
Cross-Functional Collaboration & Process Excellence: Act as a strategic partner to Marketing, Sales, Supply Chain, and QA teams, embedding regulatory requirements into business processes (e.g., Quality Agreements, TTS); maintain SOPs and compliance databases to drive operational efficiency.
Stakeholder Engagement & External Representation: Serve as the primary point of contact for Health Authorities and industry bodies, managing inspections, responding to queries, and building strong relationships to facilitate smooth approvals and negotiations.
Regulatory Intelligence & Safety Oversight: Monitor global and local regulatory landscapes (including e-commerce and sustainability trends), analyze impacts on the portfolio, and establish robust safety review processes to ensure product integrity and…