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.

About the role
As a Regulatory Affairs Lead for Southern Europe, you will be responsible for leading regulatory strategy, operations,

compliance and risk management activities across the Southern Europe markets. In addition, you will have direct responsibility for all Regulatory Affairs activities in Italy, acting as the local RA accountable.
The role reports to the Europe Regulatory Clusters & Operations Lead

Role Responsibilities
- Establish strategic direction for all regulatory processes in the Cluster countries in alignment with Operating Unit (OU) Regulatory Affairs strategy & objectives and cluster functions strategy & objectives (Commercial, Medical, etc.).
- Ensure the regulatory strategy is executed for the registration of the products intended to be placed on the cluster markets.
- Ensure the appropriate maintenance of the existing licenses.
- Ensure the advertising and promotional materials are approved (in case it is relevant) and in line with the local legislation requirements in all Cluster countries.
- Ensure regulatory contribution to the local claims’ development and localis

South Europe Regulatory Lead

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