Manager Regulatory Affairs (m/w)

Your Tasks

Development of submission of quality related documents for clinical studies (CTA); development of IMPD; compilation of applications (module 2.3 and 3); dossier compilation; co-operation with different professional groups within the company group; reporting to Head of Department Regulatory
Affairs

Your Profile

University degree in medicine, pharmacy or life science and several years of professional experience in the field of Regulatory Affairs (Pharma) in international teams with emphasis on chemically defined pharmaceuticals; Master in Drug Regulatory Affairs (DGRA) appreciated; profound knowledge of medicine; experience with inhalative medicinal products appreciated;
advanced IT skills; good command of English; good command of German and other languages appreciated; structured, thorough and detailed scientific way of working; ability to work collaboratively in a complex team environment; good organisational skills; willingness to travel

Please send your complete application documents via mail to contact@tyrell.eu under specification of your salary requirement and your earliest availability.