Stellenbeschreibung

www.daiichi-sankyo.eu Daiichi Sankyo is one of the world's 20 leading pharmaceutical companies and employs almost 32,000 people. The company's world headquarters are in Tokyo. Its European base is located in Munich, Germany. Daiichi Sankyo Europe has affiliates in 12 countries. For our Clinical Trial Supply department in our production plant in Pfaffenhofen/Ilm we are seeking highly qualified candidates to fill the position: Distribution Manager CTS (m/f) Key responsibilities: Distribution Management of Investigational Medicinal Products (IMs) – Study Project Setup * Collaboration within Global Clinical Supply Operations (US, UK and Japan) * Set up study specific distribution instructions * Set up investigational site address database * Design shipping documentation * Support project implementation into the interactive response technology system (IRT) * Determine and initiate timely orders of necessary components for distribution (i.e. temperature loggers, shippers, insulated containers, gel packs etc.) * Set up temperature logger strategy * Issue IMP & temperature logger handling instruction for investigational sites * Confirm regulatory country requirements and lead times regarding import * Act as contact person for questions related to study logistics * Ensure continuous process improvement Distribution Management of IMPs – Study Project Maintenance * Ship order management * Schedule site & depot shipments * Check shipping documents (e.g. proforma invoices, shipping protocol, courier documents, address labels, delivery note, acknowledgement of receipt etc.) * Check further accompanying documents (e.g. release documents) * Assure correctness of pick & pack processes * Supervise distribution operator(s) * Manage finished goods & components inventory * Shipment oversight * Act as contact person for shipment related questions from the clinical sites General * Assure regulatory compliance (GMP, GCP, GDP) * Maintain relevant SOPs * Manage permanent and temporary personnel * Support implementation ERP system (SAP) Professional experience and personal skills: * University degree in Natural Sciences, Pharmacy, Logistics or an equivalent qualification * At least a minimum of 5 years' working experience in a comparable position * Experience in regulatory compliance * Strong communication and interpersonal skills, demonstrable intercultural competency * Experience with GxP and Investigational Medicinal Product (IPM) would be an advantage * Open-minded, flexible and motivated * Willingness to support packaging and project management activities within Clinical Trial Supply group * Strong team player and the ability to build effective working relationships * Excellent German and English skills, both oral and written communication What we offer: We offer an interesting, diversified and challenging position, good contractual conditions, all the social benefits of a modern company and a professional environment where you will have the opportunity for personal growth. Are you interested in this opportunity? Then we look forward to your online application. Apply online >>