Expert (m/w/d) Logistic Operations Distribution - Clinical Supply Planning & Operations

With over 120 years of experience and around 19,000 employees in more than 30 countries/regions, Daiichi Sankyo is committed to discovering, developing and providing new nursing standards that enrich the quality of life worldwide. In Europe, we focus on two areas: The aim of our specialty business is to protect people from cardiovascular diseases, the most common cause of death in Europe, and the patients suffering from it, to help enjoy every precious moment of life. In the field of Clinical Supply Planning & Operations, you play a central role in the global distribution of clinical trials. You ensure that IMPs, intermediate stages, finished products and laboratory samples reach their destinations efficiently, compliant and on time. You work closely with international partners in Japan, the USA and Europe. From now on we are looking for a dedicated/n for our location in Pfaffenhofen Expert (m/w/d) Logistic Operations Distribution - Clinical Supply Planning & Operations Position: In the field of Clinical Supply Planning & Operations, you play a central role in the global distribution of clinical trials. You ensure that IMPs, intermediate stages, finished products and laboratory samples reach their destinations efficiently, compliant and on time. You work closely with international partners in Japan, the USA and Europe.

Coordination and processing of the logistics for clinical trials (IMPs), pharmaceutical stages, finished products and laboratory samples Compilation of shipping and customs documents as well as implementation of shipment processing within the EU and worldwide Provision and control of all materials and documents required for the dispatch of clinical trials appointment planning in coordination with sponsors and courier services Contact person for correspondence for document creation and for requests for shipments (e.g. client, importer of record, customs, recipient); including tracking of shipments Implementation of return processing and goods orders in SAP Maintenance of data, documents and stocks in SAP, ICSM, MS Access, Excel and IRT systems Collection of offers and implementation of the audit and clearance ensuring GMP compliance; Creation, revision and further development of work instructions and specification documents Close cooperation within the Global Clinical Supply Operation (Japan, USA, EU) Working on the continuous optimization of work processes Ensuring compliance with all GxP requirements (GMP, GCP, GDP) as well as legal and regulatory requirements

Complete university studies in pharmacy, natural sciences, logistics or a comparable qualification Multiannual professional experience in a comparable position, ideally in the GxP-regulated environment Experience in dealing with Investigational Medicinal Products (IMPs) and temperature-controlled shipments High interaction and communication skills, especially in the international environment (e.g. cooperation with teams in Japan and the USA) Impressed team orientation and ability to build trustful and effective working relationships Self-responsible, reliable and structured operation High flexibility in handling changing priorities and requirements Very good IT skills (MS Office, SAP) as well as a strong technical understanding and high affinity for standards and guidelines Very good knowledge of German and English in word and writing (e.g. creation of English-language documents and correspondence) Compliance with the Air Safety Authority Reliability Test criteria