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.

About the Role

As a CS Science Specialist, you will contribute directly to the ongoing monitoring and evaluation of product safety across clinical development and post-marketing settings.

Your work will help ensure that safety information is assessed accurately, potential safety signals are identified and escalated appropriately, and high-quality safety documentation is delivered in line with global regulatory and compliance requirements.

You will work with information from multiple sources to understand emerging safety topics, support safety evaluations and contribute to regulatory and product labelling activities. The scope goes beyond a single area of safety science, giving you exposure to clinical studies, real-world evidence, post-authorisation safety studies, pharmacoepidemiological studies and other product safety activities.

You will also have the opportunity to contribute to cross-functional project teams and Consumer Safety process improvement initiatives, working with guidance and support from more senior colleagues as you build your expertise.

Key responsibilities

In this role, you will:

• Monitor the safety of assigned products and perform signal detection activities, using approaches such as signal management tools, literature reviews and individual case awareness tools.
• Gather and evaluate relevant safety information from appropriate sources and database searches to investigate potential signals, clearly documenting, communicating and escalating outcomes.
• Prepare accurate, fit-for-purpose safety evaluation documents with clear conclusions, including responses to internal requests and regulatory authorities.
• Contribute to the safety elements of regulatory submissions, including submissions for new products, formulations or indications, as well as documentation supporting licence renewals.
• Provide safety input into development programmes covering areas such as clinical studies, real-world evidence, post-authorisation safety studies, pharmacoepidemiological studies and sensory studies.
• Support risk minimisation and product information activities, including umbrella branding assessments, product labelling and documentation required for labelling updates.
• Support the preparation of safety-related documentation, which may include the safety components of Safety Data Exchange Agreements.
• Maintain readiness to support internal audits and regulatory inspections.
• Represent Consumer Safety Science on cross-functional project teams, with appropriate guidance, and contribute to initiatives aimed at improving Consumer Safety processes.

Qualifications and skills

Essentials

You will bring a degree in a biomedical or healthcare-related discipline together with a foundation in safety science and an interest in developing your expertise further.

For this role, you will need:

• knowledge of medical and drug terminology, together with an understanding of causality assessment and methodologies used in safety evaluation and risk management;
• foundational knowledge of the relevant regulatory environment and regulations applicable to different product types;
• an understanding of the relevant therapeutic area and related disciplines, including areas such as statistics;
• the ability to communicate scientific and safety information through clear and accurate medical writing;
• confidence using computing tools and working with different sources of information to investigate safety questions;
• the ability to assess available information, identify potential approaches and make decisions in consultation with others when appropriate;
• strong relationship-building skills and the ability to work effectively with stakeholders on product safety topics.

You do not need to approach every safety question alone. The role involves collaboration and consultation, with guidance available from more senior colleagues where appropriate.

   

    

PLN 144 672,00 - PLN 198 924,00 The salary range for this position is indicative and provided as a guide. The final offer may vary depending on factors including relevant experience, skills, qualifications, and internal equity considerations. Further details regarding the total reward and benefits package will be shared during the recruitment process. Salary ranges may vary by location in line with local market conditions and applicable pay transparency regulations. Compensation information is shared for the primary location of this role. Where the position is advertised with additional locations the compensation range will be discussed during the recruiting process.

   

 

 Job Posting End Date

 

 

2026-09-27

 

 

 

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.