Senior Regulatory Affairs Manager (UK/Ireland) in London

At Perrigo, we are driven by our mission to make lives better through trusted health and wellness solutions, accessible to all. We are proud to be a Top 10 player in the European Consumer Self-Care market and the largest U.S. store brand provider of over-the-counter and infant formula. Dedicated to providing the best self-care for everyone, we are the people behind the brands you trust. We are committed to enhancing the wellbeing of our colleagues and consumers alike. We pride ourselves on fostering an inclusive, collaborative culture where each person can experience a sense of belonging.

As a key member of the Europe North Cluster Regulatory Affairs Team, the Senior Regulatory Affairs Manager will have oversight and accountability for regulatory licensing and post-marketing regulatory activities for all products marketed within the UK & Ireland. In this role, you will be responsible for ensuring strategies and relationships with local authorities align with the business needs of Perrigo Europe North Cluster with a particular focus on the UK & Ireland.

• Ensure the company's regulatory affairs activities are conducted according to relevant regulations, laws, and standards.
• Oversee the company's regulatory application process to obtain all necessary permits, licenses, certificates, authorizations, etc.
• Establish and maintain good relationships with regulatory authorities, trade associations, and internal stakeholders.
• Ensure appropriate basis to marketing strategies are identified and/or implemented; assist in identification of advanced regulatory strategies for all regulatory classifications, with a focus on medicinal products and medical devices.
• Provide advisory to the company's management on emerging regulations and developments in the industry, particularly in the field of medicinal products and medical devices.
• Manage a team of regulatory affairs professionals.

• A scientific degree in a pharmaceutical, chemical or biological discipline.
• 8 years of Regulatory Affairs experience, ideally within UK OTC including Post Marketing Licence Maintenance activities, renewals, and safety updates.
• Must have leadership experience and strong experience in medicinal products.
• Experience from launching new products and interactions with PAGB and ClearCast.

We believe our people are our greatest asset. Alongside competitive compensation, we offer benefits tailored to supporting you and your family, as well as career development opportunities to ensure you feel valued and supported, both professionally and personally.

We love our offices and the setting they provide for in-person collaboration and celebration. But we also appreciate the opportunity to work remotely can energise you too, so we promote flexibility with the ability to work two days a week from home in many roles.

We are proud to be included in the Forbes list of 'America's Best Employers by State 2024'.

We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law.