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!