• Collecting and coordinating information and preparing regulatory documentation for submission to regulatory agencies, authorities or to commercial partners.• Scientific/Medical and CTD writing and preparing regulatory documents required during registration of medecines. • Maintain a thourough and current knowledge of national and international regulation, guidance and standards applicable to company products.• Elaboration of Procedures, instructions and specification… Show more • Collecting and coordinating information and preparing regulatory documentation for submission to regulatory agencies, authorities or to commercial partners.• Scientific/Medical and CTD writing and preparing regulatory documents required during registration of medecines. • Maintain a thourough and current knowledge of national and international regulation, guidance and standards applicable to company products.• Elaboration of Procedures, instructions and specification sheets following GMP guidance. • Participating in developing the quality management system and getting ISO certified. (ISO 9001, ISO 22000 HACCP) Show less

- Élaboration d'un plan d'action Marketing B2B et B2C.- Inbound and outbound marketing Statergy. - Digital Brand Content - New product development, Sourcing, Competitors investigation, Design and Launching.

Free-lance corporate, Specialized in Branding and digital marketing.