Senior Regulatory Specialist - Self Care At Kenvue, we realize the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we re the house of iconic brands - including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON S and BAND-AID that you already know and love. care is our talent. Our global team is 22,000 brilliant people with a workplace culture where every voice matters, and every contribution is appreciated. We are passionate about insights, innovation and committed to delivering the best products to our customers. We put people first, care fiercely, earn trust with science and solve with courage and have brilliant opportunities waiting for you! Hybrid Senior Regulatory Affairs Specialist Self-Care This position is reporting to EMEA Regulatory Science & Advocacy Director. At Kenvue, we realise the extraordinary power of everyday care. Built on over a century of heritage and rooted in science, we re the house of iconic brands - including NEUTROGENA, AVEENO, TYLENOL, LISTERINE, JOHNSON S and BAND-AID that you already know and love. care is our talent. We put people first, care fiercely, earn trust with science and solve with courage and have brilliant opportunities waiting for you! As a Senior Regulatory Affairs Specialist Self-Care, you will be part of the EMEA Regulatory Science & Advocacy team and you will support regulatory intelligence, policy development, external engagement, and cross functional alignment. You provide clear regulatory insights to help guide strategic decisions in the evolving EU self care environment. Regulatory Intelligence & Foresight Monitor regulatory developments from EMA, HMA, CMDh, the European Commission, and national competent authorities. Track topics such as EU pharmaceutical legislation revision, Rx to OTC switches, labelling and packaging rules, pharmacovigilance, benefit risk considerations, and quality standards. Provide concise analyses to support business preparedness. Regulatory Policy Contribution Contribute to company positions on EU regulatory and policy initiatives affecting the self care landscape. Ensure EMEA specific insights are reflected in global regulatory and policy discussions. Support development of advocacy materials and briefing documents. External Advocacy & Representation Participate in industry association working groups and relevant regulatory or policy platforms. Contribute scientific and regulatory expertise to help shape proportionate, consumer centric, and innovation friendly frameworks for OTC medicines. Collaborate with Regulatory Affairs, Medical, Quality, Legal, Government Affairs, R&D, and Commercial teams. Communicate regulatory changes clearly and pragmatically. Provide regulatory assessments to support decision making and internal governance processes. Help ensure organizational readiness for evolving regulatory expectations. Relevant bachelor s degree or higher in Regulatory Affairs, Life Sciences, Pharmacy, Law, Public Policy, or related field. Minimum 5 years of experience with EU regulatory frameworks for self care and OTC products. Strong understanding of EU regulatory processes and interactions with competent authorities. Proven ability to interpret complex regulatory texts and translate them into actionable guidance. Fluency in English. Competitive Benefit Package Paid Company Holidays, Paid Vacation, Volunteer Time, Summer Fridays & More! Extensive Learning & Development Opportunities All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identify, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability. #If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation.