Regulatory Affairs Manager GB&I

Haleon plc.; Greater London; On-site; GBP 80,000 - 105,000; Full time

Job summary

Haleon plc seeks an experienced Regulatory Affairs Manager to manage a defined GB&I product portfolio, ensuring proactive compliance with UK, Irish and European laws. You will oversee submissions, claims advice, and labeling while coordinating with internal teams and external agencies.

Based in London Bankside with three onsite days, you will drive regulatory strategy, maintain systems, and mentor staff to meet business targets and ensure safe, compliant product launches across consumer health

Qualifications

• Degree in pharmacy, chemistry or life science with proven regulatory experience.
• 5+ years in Regulatory Affairs, including OTC, with UK/EU knowledge.
• Familiarity with PAGB Code of Practice and advertising rules.
• Experience with electronic regulatory submissions and document management systems.
• Strong planning, organization and prioritization for high-volume workloads.
• Customer-focused, collaborative team player with clear communication.

Responsibilities

• Lead regulatory activities for defined product portfolio in GB/I, ensuring timely compliance.
• Provide advice on product claims, copy and labeling and support submissions.
• Train and guide staff on regulatory affairs and systems usage.
• Ensure timely maintenance, renewals and PV activities within set timelines.
• Set priorities in changing contexts and coordinate with matrix teams.
• Collaborate with Regulatory Agencies and cross-functional partners for approvals.
• Contribute to regulatory strategy and filing plans to minimise development time.
• Drive process improvements and maintain internal SOPs and work instructions.

Skills

Leadership

Communication

Time management

Team player

Regulatory knowledge

Education

Degree in pharmacy, chemistry or life science

Tools

Electronic regulatory submissions systems

Document management systems

Job description

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.

JOB PURPOSE

• To manage a defined portfolio of products within the GB&I Regulatory Affairs Group to ensure proactive and timely compliance with all UK, Irish and European legislation and ensure that all regulatory activity is planned and geared to support and deliver commercial requirements.
• To identify and communicate regulatory issues which have the potential to affect the competitive impact of Consumer Healthcare products in the UK and Ireland.
• Provision of an effective regulatory service to allow OTC medicines, medical devices, cosmetic products and food supplements to be legally sold in the UK and Ireland with strong claims which can be supported.
• To facilitate the launch of new cosmetic, medical device, medicinal and food supplement products, and to ensure that appropriate new Marketing Authorisations are obtained where necessary to allow continued and future sale of Consumer Healthcare products in GB&I (as relevant to portfolio).
• To help ensure that regulatory activities are planned and geared to commercial requirements.
• To ensure all regulatory maintenance activity, pack copy and advertising for the GB&I business is managed to comply with the regulations and relevant company requirements.

ROLE GRADE: 7

Key Responsibilities:

• Responsible for ensuring that medicinal, medical device, cosmetic and food supplement products can be legally sold and supported in compliance with regulations.
• Provide advice, recommendations and support for product claims, copy and labelling.
• Responsible for ensuring that all personnel are given adequate training and guidance in all aspects of regulatory affairs work, and to ensure that all regulatory systems and databases are up to date and effectively managed.
• Ensures quality of both own and submission team work and compliance with regulatory guidelines and process within the required timelines. Responsible for the maintenance activities associated with a defined portfolio, including product renewals, and routine PV activity.
• Sets and resets priorities in rapidly changing circumstances and works with other team members to maintain focus and deliver objectives.
• Creates and maintains good working relationships within the Business and across Global Regulatory (GRA) functions, as well as other support functions, including factories and GMS teams, Quality, R&D, and with influential external bodies (Trade Associations and professional bodies).
• Leadership of, preparation and review of day to day submissions with full accountability for delivery. May also take accountability for larger projects as part of a broader project plan i.e. line extensions, global strategic projects, system changes etc.
• Contribute to the assessment of new innovation projects and exploratory product development briefs.
• Working either independently on Regulatory Strategy or with Category Regulatory Representatives, to help develop the regulatory strategy or components of filing strategies designed to minimise time for development and regulatory approval and optimise competitive positioning and global opportunities.
• Required to liaise with Regulatory Agencies to resolve issues in relation to their accountabilities and lead regulatory interactions.
• To support effective change management and to progress artwork changes through the Artwork Management System in line with requirements.
• Identifies, challenges, develops and implements written procedures (e.g., local SOPs, work instructions), and proactively highlights opportunities for process improvement.
• Responsible for highlighting own training needs and working with his/ her manager to develop a training plan and achieve training goals.

BASIC QUALIFICATIONS:

Business Skills & Competencies

• Degree in pharmacy, chemistry or life science.
• Minimum of 5 years relevant experience in Regulatory Affairs, (including OTC regulatory experience), and with an excellent knowledge of EU and UK medicinal, medical device and cosmetic regulatory requirements.
• An in-depth knowledge of the PAGB Code of Practice, together with an excellent working knowledge of other advertising Codes and labelling guidelines.
• Previous experience with electronic regulatory submissions and document management systems.
• Strong organisational and planning ability to organise and prioritise a high volume of work so as to ensure that all regulatory activities meet business targets.
• Strong customer focus and good team player who has the ability to work with a large group of people.
• An excellent communicator who ensures that marketing expectations are met with ongoing communication. Confident and capable of resolving conflict situations.
• Ability to foster strong matrix working. Facilitates dialogue between team and matrix members so they understand links between their different ideas and perspectives. Brings team members into the discussion so they can contribute their ideas. Capable of developing and recommending strategies for change. Developing personal networks, within Haleon and capable of using them to secure appropriate support and outcome for a project.
• Capable of identifying project or team issues in advance and seeking necessary help and support to resolve. Ability to derive creative solutions to regulatory problems, while balancing the expectations of a variety of stakeholders and ensuring compliance with regulation.
• Show a constant focus on improving performance and excellence in all tasks. Challenges and questions ways of working to seek improved process. Seeks to raise levels of performance by establishing or improving process.

Behavioural Skills & Competencies

• High learning agility, and has the ability and willingness to deal effectively with first-time situations or changing conditions.
• Self-reliant, flexible, with good time management skills with ability to operate in an empowered environment with limited guidance.
• Be able to demonstrate highly effective oral and written communication skills at all times. Capable of delivering key communications with clarity, impact and passion.
• Prioritises work to remain focused on objectives in rapidly changing circumstances.
• Ability to identify and clarify problems for assigned tasks and implement appropriate solutions.
• Team player and ability to work in a matrix environment.
• Demonstrates the flexibility to manage multiple projects in complex virtual /global environments and ability to work within cross-functional teams.
• Track record of delivery against objectives and deliverables.
• Strong leadership skills with proven ability to influence, network and negotiate with key internal / external stakeholders.

This role will be based in London Bankside (UK) with 3 days a week onsite

Job Posting End Date

2026-10-09

Equal Opportunities

Haleon are committed to mobilising our purpose in a way that represents the diverse consumers and communities who rely on our brands every day. It guides us in creating an inclusive culture, where different backgrounds and views are valued and respected – all in support of understanding and best serving the needs of our consumers and unleashing the full potential of our people. It’s important to us that Haleon is a place where all our employees feel they truly belong.

During the application process, we may ask you to share some personal information, which is entirely voluntary. This information ensures we meet certain regulatory and reporting obligations and supports the development, refinement, and execution of our inclusion and belonging programmes that are open to all Haleon employees.

The personal information you provide will be kept confidential, used only for legitimate business purposes, and will never be used in making any employment decisions, including hiring decisions.

Adjustment or Accommodations Request

If you require a reasonable adjustment or accommodation or other assistance to apply for a job at Haleon at any stage of the application process, please let your recruiter know by providing them with a description of specific adjustments you are requesting. We’ll provide all reasonable adjustments to support you throughout the recruitment process and treat all information you provide us in confidence.

Note to candidates

The Haleon recruitment team will contact you using a Haleon email account (@haleon.com). If you are not sure whether the email you received is from Haleon, please get in touch.