Senior Regulatory Affairs Manager (UK/Ireland)

Location: At Perrigo, we are driven by our mission to Makes 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 Opill®, Compeed®, Solpadeine®, NiQuitin®, and many more. We Are Perrigo . 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. Join us on our One Perrigo journey as we evolve to win in self-care. Description Overview As a key member of the Europe North Cluster Regulatory Affairs Team, the Senior Regulatory Affairs Manager will have oversight and accountability for regulatory licencing and post marketing regulatory activities for all products marketed within 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 UK & Ireland. Scope of the Role Ensure 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 relationship with regulatory authorities, trade associations and internal stakeholders. Ensure appropriate basis to marketing strategies are identified and/or implemented; assists in identification of advanced regulatory strategies for all regulatory classifications, with focus on medicinal products and medical devices. Provide advisory to company’s management on emerging regulations and developments in industry, particularly in the field of medicinal products and medical devices. Manage a team of regulatory affairs professionals. Experience Required A scientific degree in a pharmaceutical, chemical or biological discipline. 8 years Regulatory Affairs, 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. Benefits 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. Find out more about Total Rewards at Perrigo. Hybrid Working Approach 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". Find out more here Applicants please note: To apply to this position please click the APPLY button at the bottom of the application. (The SAVE button will only save your profile information but not submit an application for this open position.) Thank you. We are an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or other characteristics protected by law. #weareperrigo