Job Description

Home to the world's best loved and trusted hygiene, health, and nutrition brands. Our purpose defines why we exist: to protect, heal and nurture in the relentless pursuit of a cleaner, healthier world. We are a global team united by this purpose. Join us in our fight to make access to the highest quality hygiene, wellness, and nourishment a right and not a privilege.

Research & Development

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In Research and Development, we're full of highly skilled talents that include Scientists, Engineers, Medical, Clinical and Regulatory professionals - all working to create a cleaner, healthier world. With nine Centres of Excellence, we continually seek out new opportunities by using science, our entrepreneurial flare and our fearless innovation to develop and enhance our existing portfolio, never compromising on quality or performance.



We do the right thing, always, by ensuring we act with responsibility and integrity, by complying with regulatory legislation across the globe, whilst ensuring our products are safe for our consumers and are to the highest quality.



The size of our organisation means you'll have the opportunity to learn and work in different functions within R&D, giving you exposure to different disciplines, teams and environments. You will also have access to our Research and Development Academy, designed to develop our team and allow you to grow in our great organisation.

About the role

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As a key specialist of our Global Regulatory Operations, Medicines Post Launch Team, you will support with the strategy and execution of key compliance projects and post-launch activities for our existing portfolio of Medicinal products. You may also be asked to support work within a different classification area from time to time. In your role you will ensure operational excellence of your area of responsibility and will deliver activities in a timely manner to a high standard in line with our operating model and internal best practice.

Hiring Manager - Will Ratcliffe

Closing Date - 3rd August 2025

We reserve the right to close this vacancy once sufficient suitable applications have been received. We advise applying early to avoid disappointment as applications will be reviewed regularly

Your responsibilities

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Supporting a complex and diverse set of regulatory requirements and landscape overview across multiple markets to enable dossier maintenance and compliance post launch.

Responsible for delivery of high quality submissions to agreed operations time frames and collaborating across partner functions to ensure timely delivery of all information required.

Supporting non dossier maintenance activities e.g. GMP documentation support for any/all of the Reckitt medicinal manufacturing sites globally

Ensuring all activities are performed in line with the operating model and internal best practice including the compliant use of all systems to ensure audit readiness at all times

The experience we're looking for

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Degree in a relevant scientific discipline - such as Chemistry, Biological Sciences, Microbiology, Pharmacy.

Some knowledge of the Regional and Global regulatory environment

An ability to support work on multiple projects at any given time and a capability to prioritise and manage your own workload independently, seeking support from the regulatory project lead as needed.

Strong communicator able to liaise with stakeholders of all levels

Agile and can demonstrate this by being able to work across different classifications as needed (with supervision and guidance where required).

A creative, results focused individual with a passion for working collaboratively and with empathy with cross functional teams, built on technical credibility, trust and strong relationships.

The ability to consistently deliver work to time, cost and quality standards in a high-pressure environment.

You strive for a high level of accuracy in authoring and or reviewing documentation for regulatory purposes, with a focus on ensuring the level of registered information is appropriate.

Able to review and summarise regulatory /technical information both orally and in written communications.

What we offer

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With inclusion at the heart of everything we do, working alongside our four global Employee Resource Groups, we support our people at every step of their career journey, helping them to succeed in their own individual way. We invest in the wellbeing of our people through parental benefits, an Employee Assistance Program to promote mental health, and life insurance for all employees globally. We have a range of other benefits in line with the local market. Through our global share plans we offer the opportunity to save and share in Reckitt's potential future successes. For eligible roles, we also offer short-term incentives to recognise, appreciate and reward your work for delivering outstanding results. You will be rewarded in line with Reckitt's pay for performance philosophy.

Equality

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We recognise that in real life, great people don't always 'tick all the boxes'. That's why we hire for potential as well as experience. Even if you don't meet every point on the job description, if this role and our company feels like a good fit for you, we still want to hear from you. All qualified applicants will receive consideration for employment without regard to age, disability or medical condition; colour, ethnicity, race, citizenship, and national origin; religion, faith; pregnancy, family status and caring responsibilities; sexual orientation; sex, gender identity, gender expression, and transgender identity; protected veteran status; size or any other basis protected by appropriate law.