Regulatory Operations Specialist - Medicines in Hull

We are Reckitt, 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.

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.

The Regulatory Operations Specialist plays an essential role in a team that works across the medicinal regulations to deliver high quality variation packages efficiently. You will ensure appropriate levels of detail within the files for internal purposes and ongoing maintenance activities throughout the full product lifecycle. You will ensure business agility in manufacture and supply activities and will strive to maintain an excellent level of compliance for our products globally. You will ensure that all regulatory dossier activities are completed according to the best process, in a consistent approach across projects. You will work alongside a wide range of cross functional stakeholders including the RAS Global function, Medical, R&D, Supply, Quality and Marketing.

Your responsibilities:

• 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.

Key Challenges:

• Working in a fast paced FMCG environment to ensure that a product remains compliant during its lifecycle post approval, with no loss of supply due to a regulatory reason.
• Keeping on top of the ever changing regulatory environment and ensure that all relevant information is applied to all necessary product and dossier updates.
• Meeting business / project deadlines in a pressurised environment.
• Building relationships across Regulatory, the wider R&D community, and supply functions within Reckitt.

The experience we're looking for:

• Regulatory affairs experience, including dossier creation and global product registrations.
• Knowledge of regional and global regulatory requirements and their impact on dossiers and registrations.
• Preparing and submitting dossiers for medicinal product registrations and supporting documentation.
• Managing multiple projects simultaneously, including workload prioritization within a team environment.
• Knowledge of global product development, product maintenance, and regulatory requirements impacting dossier maintenance.
• Bachelor's or Master's degree in a relevant scientific discipline, such as Chemistry, Biological Sciences, Microbiology, or Pharmacy.
• Working collaboratively with cross-functional teams to achieve regulatory and business objectives.
• Delivering outcomes to agreed timelines, quality standards, and project requirements in a fast-paced environment.
• Authoring and maintaining accurate regulatory documentation and dossier content.
• Communicating regulatory information and requirements to a range of stakeholders.

The skills for success:

• Regulatory, Task Execution Under Pressure, Business Acumen, Commercial Awareness, Objective Setting, Accountability, Consumer Insight, R&D, Product Lifecycle Management, Intellectual Property, Business Partnership, Collaboration and partnership building, Adapt to changes in technological development plans, Ability to challenge the status quo and propose improvement, Innovation Processes.

What we offer:

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: 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.