Reckitt Benckiser Group Location:
Kingston upon Hull
A fantastic opportunity is available to be part of a truly global transformation program, supporting the business transformation to RB 2.0. You will be leading the team which will actively lead and collaborate across a range of business functions including Tax, Legal, IS and Finance centrally and locally to develop the plan for the business unit separations across 50+ markets and support the development of the Health Hub as part of Project Gemini.
The work entails leading IMEX and CDO teams through the programme and regulatory activities associated with legal entity restructuring, including mapping of ongoing projects and regulatory environment changes to deliver the right regulatory inputs and develop strategies to perform appropriate activities to separate into Health and Hygiene Home business units.
You will develop the required plans for both legal entity restructuring activities and change of ownership for products and factories as necessary for each individual market, giving regulatory strategic advice and project delivery to the central team functions in line with business strategies.
You will support the business and local regulatory teams in markets in key regulatory activities relating to restructuring entities within the markets and consider any regulatory environment changes as well as ongoing project interactions which may impact the programme delivery whilst partnering with the tax, finance and legal teams to finalise strategies and perform the structural changes required for RB2.0 and ensuring visibility to the stakeholders within the project team and for the programme review board.
Is this You?
With a Life Science or Chemistry degree, or equivalent, youll have extensive Regulatory or R&D experience with Consumer products including proven expertise in notification or maintenance of regulatory dossiers or technical documentation including manufacturing and logistics licenses used in external regulatory applications.
Knowledge of the Regional and Global regulatory environment and how it impacts regulatory dossiers and registrations
Experience or knowledge of business change programs, with a focus around change of ownership applications for regulatory products is beneficial
Experience in preparing and submitting regulatory dossiers, updates/variations.
Experience working across different classifications of products is beneficial (e.g. medicines, medical devices, biocides, cosmetics, etc.)
Knowledge of global drug/device or consumer product rules, regulations and guidelines.
Experience in solving regulatory issues, and appropriate timely escalation and communication of problems impacting programs
Excellent cross functional senior stakeholder management
In Return RB offer very competitive salaries with excellent benefits and the chance to progress your career within a truly Global organisation.
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