Responsibilities - Support for new projects in collaboration with R&D, Marketing and Project Management - Review of possible claims and communication opportunities for new projects or products already in the market - Establish synergies between the different local regulatories with a global approach for the development of any new project. - Ensure regulatory compliance of all the products (ingredients permitted, allowed quantities, etc) in local and global formulations. - Control and adaptation to new regulations. - Preparation of packaging texts, review of proposal and approval of final artworks. - Coordinate between the different local regulatories for the multilingual packaging project. - Supervision and/or preparation PIF, TD, eCTD dossiers. Life cycle maintenance of these dossiers. - Registration and notifications tasks of different products (food supplements, cosmetics, medical devices or OTCs) prior to its commercialization. - Request of different national codes required for commercialization. - Verification of the communication of marketing materials, websites, etc - Direct contact with Regulatory bodies and consultants. - Direct contact with RoW partners to provide all the information and documents necessary for registration of products abroad. - Post-market surveillance activities for medical devices. Coordinate with PV department for OTCs and medical devices. - Management of information (databases, SOPs) according applicable ISO requirements (22000, 14001, 13485) Sector: Industria Farmacéutica Función: Salud / Medicina