Regulatory Affairs Project Manager

Hello. Were Haleon. A new world-leading consumer health company. Shaped by all who join us. Together were improving everyday health for billions of people. By growing and innovating our global portfolio of category-leading brands including Sensodyne, Panadol, Advil, Voltaren, Theraflu, Otrivin, and Centrum through a unique combination of deep human understanding and trusted science. Whats more were achieving it in a company that were in control, an environment that were co-creating, and a culture thats uniquely ours. Care to join us? It isnt a question. With category leading brands such as Sensodyne, Voltaren, and Centrum built on trusted science and human understanding, and combined with our passion, knowledge, and expertise, were uniquely placed to do this and to grow a strong, successful business. This is an exciting time to join us and help shape the future. Its an opportunity to be part of something special. About the role Are you interested in a Regulatory Affairs role in a dynamic, fast, and flexible company? If so, this position could be an ideal opportunity to explore. This role will provide YOU the opportunity to lead key activities to progress YOUR career by joining a collaborative team of regulatory professionals. Your responsibilities include some of the following: E2e management of regulatory projects ensuring timely submission and successful approval. Participating in cross-functional projects, being the LOC Regulatory first point of contact for QSC, CMC, CMO, and internal manufacturing sites. Management of local product information updates in accordance with GDS, being the LOC Regulatory first point of contact with the global labelling team. Management of medicinal product upgrades, e.g., new indication, switch RX to OTC, improved formulation, new claims. Qualifications & Skills Relevant previous experience (6 years) in a pharmaceutical/healthcare company. Strong knowledge of pharmaceutical laws and regulations and fluent management of the lifecycle management. Knowledge of the fundamentals of medical devices. Scientific Degree (Pharmacy, Pharmaceutical chemistry, Chemistry, or related disciplines). Fluent in English. Preferred Good team player with strong interpersonal skills to work well in cross-functional teams. Works with a spirit of continuous improvement and innovation, creatively open to new ideas and methods. Results-driven mindset and problem-solving skills. Ability to work in a fast-paced, dynamic environment managing multiple priorities. Please save a copy of the job description as this may be helpful to refer to once the advert closes. Diversity, Equity, and Inclusion At Haleon, we embrace our diverse workforce by creating an inclusive environment that celebrates our unique perspectives, generates curiosity to create unmatched understanding of each other, and promotes fair and equitable outcomes for everyone. We strive to create a climate where we celebrate our diversity in all forms by treating each other with respect, listening to different viewpoints, supporting our communities, and creating a workplace where your authentic self belongs and thrives. We believe in an agile working culture for all our roles. If flexibility is important to you, we encourage you to explore with our hiring team what the opportunities are. As you apply, we will ask you to share some personal information, which is entirely voluntary. This helps us consider a diverse pool of qualified candidates and understand our progress on inclusion and diversity. Rest assured, hiring managers do not have access to this information, and it will be kept confidential. Haleon is an Equal Opportunity Employer. All qualified applicants will receive equal consideration for employment regardless of race, color, national origin, religion, sex, pregnancy, marital status, sexual orientation, gender identity/expression, age, disability, genetic information, military service, veteran status, or any other protected class. Accommodation Requests If you require a reasonable accommodation or assistance to apply for a job at Haleon, please inform your recruiter with specific details. We will provide all necessary accommodations and treat your information confidentially. Required Experience : Key Skills Proofreading, Adobe Acrobat, FDA Regulations, Manufacturing & Controls, Biotechnology, Clinical Trials, Research & Development, GLP, cGMP, Product Development, Chemistry, Writing Skills Employment Type : Full-Time Experience : 6 years Vacancy : 1 J-18808-Ljbffr

Location: Milano, Lombardia, IT

Posted Date: 11/2/2025