RA Senior Manager OH category

About the role

The purpose of this role is to provide regulatory management, governance and expertise to one category, sub-category, brand or a portfolio of products such that our products are successfully introduced or maintained Globally. The individual will build a network of collaborative relationships within Oral Health and LOC/BU/Region and ensure all regulatory requirements are met for both innovation and the lifecycle of existing products according to the company Values. An individual may also manage a small team for which they will set a compelling vision and deliver against the sub-category strategy and mission. The role requires the individual to provide specialist regulatory advice across the Category and Function.

Responsibilities

• Develops novel regulatory strategies and influences approaches within Project Teams in order to secure competitive approvals and speed to market in conjunction with LOC/BU/Region regulatory teams.
• Provides CMC evaluations for potential changes as requested and follows up to ensure regulatory compliance including completion of appropriate internal compliance records e.g. change controls
• May supervise or mentor other team members.
• Plans, prepares and delivers high-quality regulatory files to agreed timelines.
• May lead non-product related activities within the function and input cross functionally, in order to direct new policy or pioneer new processes or improvements to company's competitive advantage.
• Support the development of the strongest claims possible aligned to consumer insight and within the regulations, ensuring risks are appropriately addressed and communicated within the CAP meetings and tools.
• Ensures compliance of their actions by adhering to global, regional and local processes, policies, SOPs and working instructions.
• Why you?
• Basic Qualification:
• 10+ years of experience
• B achelor's degree in science
• Life science, or Consumer Healthcare, or Pharmaceutically-related science, or Research and Development, or Regulatory Affairs
• Regulatory professional at this level must be skilled in scientific interpretation/evaluation/communication of technical information and an ability to interface effectively with R&D, supply chain and commercial counterparts with credibility
• Ability to work on multiple projects or tasks simultaneously. Ability to analyse data and write reports with attention to detail.
• Ability to use regulatory knowledge; use strategic regulatory thinking; ability to plan and organize regulatory pathways and critically evaluate and report.
• Working towards scientific knowledge; communication and influencing on route to market and external influencing and negotiating
• Job Posting End Date
• 2026-07-15
• Equal Opportunities

Benefits

Additional Information

Welcome to Haleon. We're a purpose-driven, world-class consumer company putting everyday health in the hands of millions. In just three years since our launch, we've grown, evolved and are now entering an exciting new chapter - one filled with bold ambitions and enormous opportunity. Our trusted portfolio of brands - including Sensodyne®, Panadol®, Advil®, Voltaren®, Theraflu®, Otrivin®, and Centrum® - lead in resilient and growing categories. What sets us apart is our unique blend of deep human understanding and trusted science. Now it's time to fully realise the full potential of our business and our people. We do this through our Win as One strategy. It puts our purpose - to deliver better everyday health with humanity - at the heart of everything we do. It unites us, inspires us, and challenges us to be better every day, driven by our agile, performance-focused culture.

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