the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines and Related of new products, with a focus on complementary medicines and medical devices. Conduct dossier due diligence and registration of complementary medicines and other human medicines. Prepare the registration applications
the relevant medicine Regulatory Authorities (Country Specific where applicable), Medicines and Related experience in Regulatory Affairs, preferably in human medicines Demonstrable experience across the product development
experience in Regulatory Affairs, preferably in human medicines - Demonstrable experience across the product development
experience in Regulatory Affairs, preferably in human medicines - Demonstrable experience across the product development
Patho-Biocatalysis Group (PBG) and the Infectious Diseases and Medicinal Plants Research Niche
To ensure legal compliance with the relevant Medicine Regulatory Authorities (Country Specific where
advantageous. Additional Requirements: Excellent oral and written communication skills; analytical and
advantageous. Additional Requirements: Excellent oral and written communication skills; analytical and
research at national and/or international conferences (oral presentations).
genomics, molecular diagnostics, and personalized medicine. Watchmaker Genomics is inviting applications