Head Regulatory and Medical Affairs Lead and manage the registration process in ensuring approvals of new products, manufacturing permits, import permits and amendments to products in the 3 countries. Contact with health authorities on regulatory conditions. Manage all Regulatory, Pharmacovigilance, Quality, Medical, Compliance & Publicity activities in the 3 countries. Monitor pharmaceutical laws and ensure operational compliance (advertising, congress, packaging, samples, pharma SOP,...). Lead a multi-country team of regulatory affairs, medical and quality experts.