As part of a team, you will prepare meetings of European Pharmacopoeia groups of experts, contribute to the preparation of working documents for these groups, contribute to the elaboration and revision of European Pharmacopoeia texts and follow up meetings with a view to publication of scientific texts and memoranda.
With an appropriate recognised qualification (see on-line vacancy notice), you have experience with methods of synthesis and control used in quality control of pharmaceutical substances and products acquired for example at university, in the pharmaceutical or a comparable industry, in a control laboratory and/or in a regulatory agency. You also have excellent knowledge of one of the Council of Europe’s official languages (English) and knowledge of the other (French).
Applications must be made in English or French using the Council of Europe on-line application system. By connecting to our website www.coe-recruitment.com you can consult the detailed vacancy notice and create and submit your application.