Arbejde Regulatory Associate Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Regulatory Associate

jobbeskrivelse:
- Administrative - Denmark - Søborg 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. Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring rapid regulatory approvals of new products and of changes to existing products in all our markets. Regulatory Affairs is a fast-changing field where no two days are alike, and the engaged employees in our unit need a unique combination of scientific insight and the ability to navigate tight deadlines and many stakeholders. That makes Regulatory Affairs a truly interesting and challenging place to work. About the department In the Modern and Human Insulins department we are responsible for all the regulatory Life Cycle Management (LCM) activities with clinical and/or labelling impact for the marketed modern insulin products (Levemir®, NovoRapid® and NovoMix®) and human insulin products. We are currently looking for a Regulatory Associate to join our department of 11 dedicated employees. The job Your primary task will be to handle the regulatory activites for one of our modern insulin products which is marketed worldwide. You will do this in close collaboration with the product responsible regulatory professional, internal stakeholders and Novo Nordisk affiliates worldwide. You will be administrative responsible for preparing, compiling and submitting documentation to health authorities, and assisting in ensuring approval of the documentation. You will also be handling requests from affiliates and other stakeholders. You will work in a fast paced environment with tight deadlines, and you will be supported by a team of friendly colleagues with a good sense of humour. Qualifications Preferably, you have some years of experience from working in Regulatory Affairs. You have an educational background as pharmaconomist, medical secretary, bachelor in science, marketing, English or similar. You have a flair for IT systems and experience with MS Office applications as you will be responsible for managing data entry and electronic filing in our various databases and document management systems. Fluency in written and spoken English is a must. On a personal level, you are very structured, systematic and you have a strong quality mind-set. You have a positive attitude and you keep your spirits high also under pressure. You can work independently, but you are also the team player who helps and cares about your colleagues and contributes to the good atmosphere in our department. 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 Dorte Tingskov at +45 3075 8086. Deadline 16 March 2015.

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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