Arbejde Supply Chain Associate Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Supply Chain Associate

jobbeskrivelse:
- Administrative - Denmark - Måløv Our growth is your opportunity Being part of Novo Nordisk Research & Development means working at one of the world's largest and most successful biopharmaceutical companies. Our R&D organisation is vital to Novo Nordisk's continued growth and we always welcome talented people who would like to grow with us. 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 might have a job for you. About the department Clinical Supplies Supply Chain Planning (CSSCP) is a key member of R&D CMC Clinical Supplies (CS) and is vital in bringing new drugs to market. Our responsibility 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 operate in the combined field of supply chain management and regulatory requirements within drug development. The job As Supply Chain Assistant in our Supply Planning Team you will assist the Supply Chain Planners who are responsible for the clinical supply chain in each trial ensuring timely and sufficient trial product for our clinical trial sites globally. The Supply Chain Assistant must efficiently execute the packaging and distribution plan across multiple trials and is furthermore responsible for several supporting processes across the trial portfolio. The main responsibilities include: Create orders and provide documentation for packaging of trial product for the clinical trials; Create shipping orders for trial product and provide required documentation; Filing and archiving of relevant trial documents; Ordering Blood Glucose meters for diabetes trials; Support stakeholders (internal as well as external) during trial conduct and make sure all trial products are destroyed when the clinical trial is closed down. Qualifications Your educational background is within administrative/planning or logistic. Ideally, you have experience from a similar job with planning or with the pharmaceutical area. Knowledge of GMP/GCP is an advantage. 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 are service minded and good at initiating and driving things. You have a good sense of humour and a positive attitude to challenges and see continuous improvement as a natural part of your job. You have excellent computer skills, are good at learning and understanding new systems and working with MS Excel and MS Project are a natural part of your work day. Experience with PMX and IWRS is an advantage. You are fluent in written and spoken English. At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development. Contact For further information, please call Søren Vodsgaard on +45 3075 2352. Deadline 1 February 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark

GÆLDER

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