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Global Regulatory Senior Associate - Nurofen NPD


As a Global Regulatory Senior Associate, you’ll support the development of regulatory strategies, its execution and dossier delivery for leading brands like Nurofen in a global frame, working with the Regulatory Senior Manager in driving regulatory expertise for the assigned projects. You will collaborate with local regulatory teams in the development of plans and project execution. 
Global Regulatory Senior Associate - Nurofen & Stepsil's NPD
Slough, Berkshire, Hybrid Working 
Competitive Salary & excellent benefits package, 25 days annual leave, Bonus, Private Healthcare, 10% Pension Contribution 

Your expertise in project management, dossier content and submission to deliver a “right first time” approach and overcoming regulatory difficulties will be paramount to enable delivery of regulatory strategies. Globally, you’ll be responsible for the management of Regulatory NPD requirements for Nurofen / Strepsil's brand. To achieve it, you’ll work collaboratively with a wide range of stakeholders like, R&D, Medical, Local Regulatory, Marketing and Supply.
You’ll succeed because…

…you’re a problem solving person willing to hear and understand others points of view. You’re culturally aware, thriving in an international context and keen to build a career in a leading global business and because you have worked in Regulatory over 5 years:
•    Have regulatory experience to manage medicinal portfolio and supporting new product development portfolio across EU.
•    Have strategic mindset to communicate the business of any regulatory challenges and risks.
•    Are proactive, results-oriented, and able to juggle multiple projects and priorities.
•    Have good oral and written communication skills and maintain high standards for quality, even under tight timings.
•    Work collaboratively with Snr Manager/Manager in order to define and implement the regulatory strategy.
•    Support key innovation initiatives as required assigned by manager.
•    Work collaboratively within R&D community to define global registration dossiers and technical documentation. If required, attend meetings with regulatory bodies in order to confirm submission requirements.
•    Work in partnership with the local regulatory teams to identify and be aware of key requirements and that they are considered to deliver a ‘right first time’ approach to new product development. 
•    Responsible for project management of Regulatory NPD requirements & dossier/technical file creation in line with the project strategy.
•    Assist in monitoring, collecting, interpreting and sharing with business partners, regulatory issues and trends that will impact RB products, policies and procedures.  Assist in the development of strategies and plans of action to address them.  
•    Assist in the preparation of responses to address significant safety ,regulatory and PR issues in the assigned Category.   

You’ll love it because…
… You’ll share your experience with and learn from experienced colleagues. The company will present you many professional-growing opportunities as you succeed in your role. You’ll be able to probe and develop your abilities globally thriving in a changing and diverse regulatory framework.




At Reckitt, 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. Come and join a team whose purpose is to protect, heal and nurture in the relentless pursuit of a cleaner and healthier world.

All qualified applicants to Reckitt 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.

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