🚀 Head of Regulatory Affairs

Join a global leader in healthcare that is dedicated to improving lives through innovation and compliance excellence. With a focus on strategic growth and transformation, this is your opportunity to work in a dynamic, purpose-driven environment and make a meaningful impact on regulatory processes and product success. About the Role We are seeking a highly experienced Head of Regulatory Affairs to lead and manage regulatory strategies across a diverse portfolio of products, including licensed medicines, cosmetics, medical devices, and food supplements. Based in Reading, this position offers a unique opportunity to drive impactful regulatory initiatives, ensure compliance with UK and EU regulations, and support strategic business transformation. Responsibilities Develop and execute regulatory strategies to ensure compliance and timely market access. Evaluate product classification, claims, and risk/benefit to guide regulatory submissions and lifecycle decisions. Prepare, review, and submit regulatory dossiers and notifications (e.g., CPNP for cosmetics) for local and international markets. Act as the primary liaison with regulatory authorities, licensing partners, and trade associations (e.g., PAGB, CTPA), ensuring effective communication across the organization. Collaborate with cross-functional teams, including Quality, Marketing, Product Development, and Supply Chain, to align regulatory input with business objectives. Oversee regulatory review and sign-off of product artwork and promotional materials, ensuring compliance with legislation and codes of practice. Maintain regulatory documentation and systems, ensuring audit readiness and compliance with Health & Safety and Quality standards. Lead and develop the Regulatory Affairs team, managing resources, supporting succession planning, and overseeing a regulatory budget of over €2 million. Required Skills Extensive experience in Regulatory Affairs, including navigating complex regulatory landscapes and supporting successful product launches and lifecycle management. Significant experience in the consumer goods industry, preferably in consumer healthcare, cosmetics, or related areas. Comprehensive knowledge of UK and EU regulatory frameworks for cosmetics, medical devices, and food supplements (experience with licensed medicines is a plus). Hands-on experience with regulatory submissions and direct interactions with health authorities. Strong communication, project management, and organizational skills, with the ability to work cross-functionally in a dynamic environment. Equal Opportunity Statement If you’re ready to make a real impact, thrive in a dynamic environment, and lead a high-performing team through strategic regulatory transformation, we’d love to hear from you. Apply now and take the next step in your career!