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Supply Chain Coordinator (Måløv, Denmark)

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Supply Chain Coordinator

- Supply Chain and Logistics
- Denmark - Måløv

Are you looking for new challenges within supply chain management? Would you like to be part of a rapidly growing part of Novo Nordisk’s R&D organisation coordinating multiple activities together with a dedicated team of colleagues? Then we have a job for you.

About the department
Clinical Supplies Coordination (CSCo) is a key member of R&D and is vital in bringing new drugs to market. In CSCo we have a unique understanding of the combination of drug development and supply chain management. Our main and most important task in CSCo is to ensure that trial products are available on time and in the right quality and quantity for all clinical trials conducted globally by Novo Nordisk. We do this in close collaboration with our stakeholders across Global Development, Regulatory Affairs, Product Supply, affiliates, and CMC Supply. In order to meet Novo Nordisk’s ambitious goals within diabetes, haemophilia and other chronic diseases, we are furthermore working with reducing our product waste, shortening our lead time and optimising the use of resources by means of various LEAN tools. We are around 50 people in Clinical Supplies Coordination and are located at Novo Nordisk site Måløv. The department is divided in four teams (Diabetes Planning, Diabetes Logistics, Biopharm Planning and Biopharm Logistics). The open position is in the Diabetes Logistics team.

The job
As Supply Chain Coordinator in our Diabetes Logistics team you will be responsible for the complex clinical supply chain ensuring timely and sufficient trial product for our clinical trial sites globally. You will through efficient and timely planning decide how much product needs to be packed and available throughout the study life time, and by setting up a proper distribution strategy you will make sure we do not have stock outs on any depots or clinical sites around the world. Your responsibilities also include providing input to the specification of our web-based trial supply management system (IVRS) and supporting stakeholders globally during trial conduct with regards to ensuring trial supply availability.

Qualifications
You have an academic degree within supply chain management or logistics combined with some years’ experience from the pharmaceutical industry and a GMP/GCP regulated environment. Alternatively, you are a pharmacist with strong experience within supply chain management. You have strong analytical skills, a strong quality mind-set, communicate effectively, meet deadlines, approach tasks in a structured way and you are able to work with multiple and frequently changing priorities in a dynamic environment that is driven by the tight deadlines characterising the final phases of drug development projects. You are a dedicated team player who inspires trust amongst colleagues and partners. You have a positive attitude to challenges and see continuous improvement as a natural part of your job. You have excellent computer skills and working with MS Excel and MS Project are a natural part of your work day. You are fluent in written and spoken English.

In this position, you will be able to further develop your supply chain skills and business understanding, and you will broaden your personal competences and skills.

At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth

Contact
For further information, please contact Team leader Tanja Lund Erichsen, +45 3079 8155.

Deadline
17 November 2013.

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