Ras Senior Associate Gastrointestinal

3 weeks ago


Kingston upon Hull, United Kingdom Reckitt Full time

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**:
**About the role**:

- Want to steer the growth of a major global brand? As a RAS Senior Associate Gastrointestinal you’ll have the freedom to show us what’s possible and help drive innovation that makes an impact. Globally.**RAS Senior Associate Gastrointestinal**

**Kingston upon Hull, East Yorkshire**

**Hiring Manager: Steven Hesp (Regulatory Affairs and Safety Strategy Senior Manager - Gastrointestinal)**

**Internal Application Deadline: Wednesday 31st January 2024**

**Competitive Salary & excellent benefits package including Performance Bonus, 25 Days Holiday plus Bank Holidays, 10% Pension Contribution, Private Healthcare, Annual Salary Review, ShareSave Scheme, Hybrid Working and much more**
- You’ll play a critical role driving innovation and developing new products. You’ll navigate a complex regulatory environment. As a steward for our brands, you’ll ensure our product portfolio supports our ambitious growth plans. You’ll anticipate and influence regulatory changes and lead our thinking about what’s possible. You’ll develop global registration dossiers and technical documentation to ensure our products are safe, efficient and continue to make our customers lives better.**Your responsibilities**:

- Ensure proper representation of the Regulatory and Safety Strategy Gastro Intestinal Team in multi-functional teams
- Represent the Regulatory Function with end-to-end oversight and responsibilities of the registration / notification processes that happen around the world
- Overall accountable for the Regulatory and Safety E2E (end to end) Strategy for Gastro Intestinal projects from development, innovation and growth projects to maintenance, risk management & defence activities to meet the business objectives
- Lead the strategy with the corresponding country regulatory affairs to define development plans and timings of projects and critical regulatory parameters in data and timings
- Matrix leadership for the cross functional regulatory focus teams, including all regulatory and safety disciplines and across local teams, to ensure one voice & execution
- Accountable for the creation and delivery of the product core dossier/technical files, to achieve in market registration/launches, giving support to the rest of the team in driving consistency & direction. Ensure appropriate resources and expertise when working with the dossier/technical file authors, to ensure consistency and ‘right first time’ approach, in line with the agreed regulatory strategy and in a consistent approach across projects
- Be responsible for coordinating responses to Regulatory Agency questions
- Supports work required to refine Regulatory processes and procedures to optimise accuracy and efficiency, thus enabling speed to market
- Monitor competitive intelligence/regulatory horizon to bring ideas for category
- Working with country regulatory, support and where necessary lead Health Authority meetings/negotiations in support of submission and approval of strategic new product registrations in critical markets
- Work in partnership with the local regulatory teams to identify and be aware of key requirements and that they are taken into account to deliver a ‘right first time’ approach to new product development
- Provide strategic oversight for Gastro Intestinal projects across the full product life cycle
- Motivate and lead teams within a results-oriented culture, where personal ownership, being ‘nimble’, strong teamwork, and ‘care for colleagues’ are key
- Lead projects with a clear understanding of a broad set of registration/regulatory requirements across multiple markets meeting project objectives and milestones. Accountable of delivering project results following Reckitt’s processes and procedures. Responsible of communicate risks and progress with guidance
- Maintain oversight of own resource needs and raise any issues in advance

**The experience we're looking for**:

- You have relevant regulatory and/or safety strategic experience of Health products and across multiple product classifications and regions relevant Regulatory Experience and knowledge in NPD and dossier/technical file creation and global registrations
- You are a trusted business partner with proven track record of working closely with cross functional teams to deliver the effective execution of regulatory strategies
- You will have a sound understanding of regulatory requirements in the relevant area/classification. Share knowledge and experience with peers and cross-functional team.
- You are experienced in preparing and submit


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