Arbejde Publishing Associate in Regulatory Operations Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Publishing Associate in Regulatory Operations

jobbeskrivelse:
- Administrative - Denmark - Søborg To support the growing number of electronic lifecycle submissions we are seeking a Publishing Associate to join the Publishing Support & Archives team. Join a fast-changing environment where engaged people do their best every day to obtain and maintain market authorizations worldwide for all Novo Nordisk medicine across the globe. Our people have a unique combination of scientific insight and the ability to navigate many agendas and stakeholders. That makes Regulatory Affairs a truly interesting place to work – but also quite challenging. Are you up for the challenge? About the department The Publishing Support & Archives team is part of the Global Submission Management area in Regulatory Operations, located in Søborg, Denmark. One of our major tasks in the area is to publish regulatory submissions worldwide. The position As a Publishing Associate, you will be interacting with many stakeholders in the company in relation to planning, compiling, publishing, production and delivery of lifecycle eCTD’s, and other submission format types. On top of publishing lifecycle submissions, and in order to meet the emerging requirements, you will be an active player in the constant strive for optimising the use of our IT systems and continuously improve the compiling and publishing processes. The position requires good coordination and planning skills, accountability and the ability to work under tight deadlines. It is important to be service minded and to adapt to changes easily. We are looking for a person who enjoys structure, promptness and a dynamic environment. Qualifications You have a relevant educational background e.g. in science, business administration or languages. You have experience with professional use of IT systems and are proficient in the MS Office. Ideally, you already have extensive knowledge of document management and eCTD publishing processes as well as insight into the classical regulatory disciplines. You have an understanding of the evolving eSubmission standards, and you will work to ensure that we always deliver compliant submissions efficiently and timely to the Regulatory Agencies in the European countries. You are a strong team player, but you also enjoy working independently and as a person you thrive in a busy environment and you bring a “can do” spirit, a healthy common sense and a good sense of humour to your work – even when the pressure is on. You take initiative and thrive with joggling many tasks at the same time. You are a skilled communicator, who is able to collaborate with a lot of stakeholders and comfortable using your fluent written and spoken English on a daily basis when working with colleagues from Denmark as well as with colleagues in the Novo Nordisk affiliates. Working at Novo Nordisk 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 contact Tina Lindquist at +45 3075 9652. Deadline 15 May 2016.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Revisions- og regnskabscontrollerarbejde

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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