Regulatory Affairs Coordinator Health & Wellbeing

Detalles de la oferta

.**Full/Part Time: Full Time****Location: Mexico city based, fully remote****Business Context**Established in 2018, Unilever's US-centric Health & Wellbeing business is a collective of fast-growing, science-backed companies powering a lifestyle of wellbeing designed for a lifetime of possibilities. Comprised of Liquid I.V., Nutrafol, OLLY, Onnit, SmartyPants, Welly and Equilibra (in Italy), the Health & Wellbeing Collective operates with a start-up mindset and is supporting consumers on their proactive wellbeing journey by bringing innovative products to the market.Unilever identified Health & Wellbeing as a key growth space for the future and has built the business through a clear M&A criteria and growth strategy to €1bn+ turnover, delivering double-digit, volume-led growth quarter after quarter.You will be part of the International Expansion team which is responsible for launching H&W's brands across the world. This cross functional team has end to end responsibility for international expansion of the brands in a fast-paced environment. If you are excited about the prospect of bringing disruptive brands across the world this role is for you.**Role Details Overview**:We are looking to recruit an RA Specialist/ RA Assistant Manager to co-ordinate and drive the international expansion Vitamins, Minerals and Supplements ("VMS") brands within Health & Wellbeing business. This is a key role that will support the brand teams with the successful expansion of several existing US VMS brands into new markets.Previous experience of working in VMS and of working with multiple stakeholders across the globe, including authorities and trade associations, and functions, including regulatory, R&D, legal, safety, quality and public affairs is essential.This will report into Alexa Sarcona, H&W RA Manager International Expansion and will be based in United Kingdom or South America (Unilever Office TBC) with global cross-functional interactions.- regulatory landscape overview and regulatory management of VMS products; - formulation, ingredients, raw materials, product specifications and claims review; - review and approve packaging and marketing materials to comply with local regulations; - support with product notification/registration (dossier preparation for product notification), stability and shelf-life considerations, labelling requirements; - liaise with internal stakeholders and authorities' officers to ensure quick and quality submission dossier for notification/ registration.- Provide training/ education on regulatory matters to internal stakeholders.Ensuring relevant regulatory risk assessments are communicated to relevant functional experts to inform strategy on ingredients, formulations, and any advertising, brand promotion and communication.Working cross-functionally with internal stakeholders at global and local level to ensure business objectives are met through strong regulatory strategy and partnership


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