The Company Our client is a specialist in the manufacturer for the pharmaceutical sector. Due to growth, they are now looking to recruit a Regulatory Specialist. The Role * Manage and maintain EU, GB and EMEA authorisations of biocidal products; ensure compliance with other chemical regulations where applicable e.g. CLP; manage and maintain transitional biocidal registrations. * Submission, maintenance, changes and renewals for products under EU BPR, GB BPR and other EMEA regulations as per market requirements. * IUCLID dossier build, use of R4BP, preparation of SPCs, submission of IUCLID dossiers, preparation and submission of Poison Centre Notifications. * Supporting Quality Assurance with implementing regulatory changes e.g. label artwork and Change Controls. * Providing regulatory input for SDS preparation, marketing, sales, technical and R&D. * Attend regulatory meetings in EU and elsewhere as required. * Regulatory monitoring, including awareness of new regulations and changes to existing regulations, including internal communication of any potential impact to the company. * Maintain compliance with other chemical regulations e.g., REACH, CLP, Detergents, as applicable for product range. * Submission of annual biocidal product sales quantities to selected Member States. * Liaise with all departments, project teams, suppliers, testing laboratories, distributors, consultants and Member State Competent Authorities to co-ordinate and monitor regulatory submissions and requirements * Support other group sites with global disinfectant registrations. * Could be full time or part time depending on the person. * Could also offer remote working but site visits at least once a month or expected. The Person * Will have experience within a similar role. * Must have biocides and BPR experience. * You will have good IT Skills (Word, PowerPoint and Excel). * Be proficient in use of IUCLID and R4BP. * Good scientific communication (written and oral). * Experience with human health toxicology and environmental risk and exposure assessments would be desirable. * Experience with efficacy testing for regulatory purposes is desirable. * Experience with CLP, REACH, SDS authoring and regulatory labelling would be beneficial. The Benefits * Discretionary annual bonus. * Private Medical Insurance for you and your family. * Pension Scheme. * Corporate benefits platform and Cycle to Work Scheme. * Death in Service Benefit. * Remote or part time working