Regulatory Affairs Specialist

Kenvue is currently recruiting for a:Regulatory Affairs SpecialistWhat we doAt 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. Science is our passion; care is our talent.

Who We AreOur 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. With expertise and empathy, being a Kenvuer means having the power to impact millions of people every day.

We put people first, care fiercely, earn trust with science and solve with courage – and have brilliant opportunities waiting for you! Join us in shaping our future–and yours. For more information, click here.

Role reports to:Associate Director, Regulatory AffairsLocation:Europe/Middle East/Africa, United Kingdom, Reading, BerkshireWork Location:HybridWhat you will doRegulatory Affairs Specialist The Regulatory Affairs Specialist is responsible for all regulatory activities associated with assigned medicines within their geographical and/or brand area of responsibility.

This role involves the compilation and submission of applications (new submissions and post-approval), resolution of Health Authority questions in cooperation with other functions, and the management of post-approval commitments and variations/renewal applications as needed. What you will do - Assist in the development of regulatory strategies across the EMEA region, providing regulatory input and technical guidance on regulatory

requirements to product development teams within the Self Care franchise. - Coordinate, compile, and submit new drug applications to regulatory agencies within their geographical and/or brand area of responsibility. - Manage MRP, DCP, and Workshare submission activities for medicines. - Develop effective partnerships with R&D, Franchise (Marketing), and local regulatory colleagues. - Collect and evaluate information on regulatory

requirements for quality, preclinical, and clinical data to meet applicable regulations. - Prepare and submit regulatory submissions for the registration and maintenance of products throughout their lifecycle, according to applicable regulatory

requirements and guidelines. - Monitor the progress of the regulatory authority review process through appropriate communication with the Health Authority, seeking opportunities to expedite regulatory approvals where possible. - Prioritize, plan, and monitor allocated projects against defined timelines. - Develop and maintain a thorough understanding of the regulatory environment and supporting data

requirements.**Regulatory Compliance** - Ensure that all assigned products comply with local regulatory and quality system

requirements. - Maintain logs of communication and outcomes with regulators and other relevant internal or external stakeholders. - Stay aware of current regulations and anticipate implications and opportunities arising from changes in the regulatory environment. - Participate in the development and implementation of applicable processes, SOPs, and working instructions. - Ensure that enterprise regulatory systems are accurate and fully maintained.

- Review and escalate compliance issues, implementing relevant corrective/preventative actions locally. - Identify and implement regional process improvement opportunities and ensure the implementation of relevant global or regional regulatory initiatives. ---**Specific

Requirements** - Relevant Bachelor's Degree or higher. - 4+ years of related regulatory experience. - Represent Regulatory Affairs on cross-functional product/project teams and provide regulatory advice. - Apply organizational understanding and awareness in decision-making. *Essential Knowledge - Knowledge of the consumer healthcare environment and product development. - Hands-on experience with regulatory

requirements and registration activities for medicines in the EU/EMEA. - Understanding of regulatory frameworks and external environments, with the ability to apply these to regulatory solutions throughout the product lifecycle. - Solid understanding of regulatory, medical, safety, and quality

requirements in relevant markets. **Core Competencies:** - Excellent communication skills, capable of articulating concepts clearly both verbally and in writing, especially when simplifying complex regulatory or technical issues. - Strong interpersonal skills; able to build effective personal networks internally and externally. - Collaborative with a strong sense of ownership, accountability, and recognition for delivering results.

- Strong organizational and time management skills, with the ability to work under pressure. - Ability to work effectively in a multi-cultural, highly matrixed organization. - Proficiency in English. If you are an individual with a disability, please check our Disability Assistance page for information on how to request an accommodation. 000000.