Are you looking for a new position as a Regulatory Affairs Specialist? Do you have experience reviewing and approving promotional materials within the medical devices space? We are recruiting for a Regulatory Affairs Specialist to combine their knowledge of scientific, regulatory and business issues to enable promotional materials created and distributed in the EMEA region to meet required legislation and standards. This position requires an ability to understand and evaluate competing perspectives and provide clear regulatory guidance.The successful candidate will be based at our client''s Maidenhead site (1 day a week from home), working 37.5 hours per week on an initial 12 month contract basis. Potential to be extended or become a permanent position. Key responsibilities in this role include:The review and approval of promotional materials for marketed productsResponsible for keeping current with industry changes relating to advertising and promotion, interpreting new guidance to industry, and continuing efforts to evaluate processes within Regulatory Affairs relating to the promotion of products in EMEAMaintain up to date knowledge of regulatory requirements and communicate changes in regulatory information to project teams and senior management in a timely mannerThe Specialist will assist local EMEA personnel in local process improvements and contributes to local and/or global process improvements that relate to promotion of products Applicants will need:A higher educat