## Regulatory Associate FTC 6 monthsApplylocations: Weybridge St Georges Avenuetime type: Full timeposted on: Posted Todaytime left to apply: End Date: June 2, 2026 (13 days left to apply)job requisition id: 543930Welcome 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.Regulatory Affairs Product Lifecycle Management Associate Medicinals**FTC - Fixed Term Contract - 6 months****Weybridge St Georges****Job Purpose:**The objective of the Product Lifecycle Management (PLM) team is to co-ordinate and deliver the timely preparation of global renewal applications and safety reporting (ie PBRERs and RMPs) for the Haleon portfolio as quickly and efficiently as possible once the required data & documents are available from relevant sources, such as R&D, sites or reference markets.This role will partner with the business to deliver robust strategic and successful regulatory outcomes for the medicinal portfolio to enable committed business plans with the ability to make independent judgment and decisions in their area of responsibility. **Key Responsibilities:*** Prepare/ensure availability of high-quality documents required to support maintenance activities of product licences are completed globally, for:* Renewals,* Safety Reports (ie PBRERs and RMPs),* Licence Cancellation Requests.* Manage the execution and delivery, with close attention to detail, of ‘Right First Time’ dossiers, ensuring filings for planned initiatives are completed as planned and in accordance with market data requirements.* Partner with all associated stakeholders, i.e. CMC, Category, Clinical, Medical, Safety, Local Regulatory to manage the execution and delivery of ‘Right First Time’ dossiers, ensuring filings for planned initiatives are completed as planned and in accordance with market data requirements.* Support Market Specific Requirements and legal type documents which are applicable for all types of submissions. e.g. Power of Attorneys, Letters of Authorisation, Certificate of Pharmaceutical Products, Certificate of Free Sale, other supporting Regulatory Statements and arrange legalisation with Foreign Office/Embassies as required.* Display ability to minimize impact by communicating and escalating to peers and senior management when required.* Comply with relevant Regulatory SOPs and systems.**Knowledge*** Expertise in using IT systems* Critical assessment of processes and systems, initiates improvements as required.**General*** Act as Regulatory representative on project teams, as required, understanding and applying project management tools.* Support processes to improve ways of working /communication.This is a role that requires a basic understanding of what Regulatory Affairs is and how this fits within the lifecycle of a product.**Job Posting End Date**2026-06-02
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