Arbejde Regulatory Project Manager Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Regulatory Project Manager

jobbeskrivelse:
- Research & Development - Denmark - Søborg Join a fast-changing environment where engaged people do their best every day to get Novo Nordisk medicines approved 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 challenging. Are you up for the challenge? About the department RA Biopharm- hGH is part of Regulatory Affairs. In our area we are a dedicated and diverse team of 30 people located in Søborg, Denmark. As a team, we are breaking new ground within the therapeutic areas of growth hormone and hemophilia. Furthermore, we are supporting all marketed products with growth hormone, Hemophilia and hormone replacements. In this dynamic environment, our dedicated group prepares the regulatory strategies and is responsible for global interactions with regulatory authorities. We work closely with many different stakeholders within Novo Nordisk headquarters and affiliates. We have a strong team-spirit and together we go the extra mile to succeed. The Job The position is situated in Søborg. As a Regulatory Project Manager you will be part of an extend project team for 1-2 projects in different stages of development/life cycle management. You will head up 1-2 regulatory teams consisting of experienced Regulatory Professionals and Associates and you are expected to diligently secure theregulatory input to global regulatory strategies and submissions. Furthermore, you will plan, coordinate and review regulatory documentation and support internal working groups. To this end, you will work closely with the Project Director who is overall responsible for the projects. In addition, you will be part of cross functional teams sharing your knowledge and getting new ideas and you will report to the department director. Qualifications As a minimum, you have a Master’s degree in biology/health science plus extensive experience from the pharmaceutical industry working with regulatory aspects in the full life cycle of a project/product. You can document solid scientific understanding and you have successfully worked in project teams respecting the contribution of everyone. You have demonstrated that you are organised, detail-oriented and a proactive problem-solver. You communicate well and are completely comfortable speaking and writing English and dealing with international communication comes easy to you, On a personal level, you thrive in busy and changing circumstances and bring a can-do attitude and a healthy sense of humour. You keep focus on jointly moving the projects and are able to work independently, be challenged and find new solutions. 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 Eva Gamwell Henriksen +45 3079 6202. Deadline 18 June 2015.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse:
Arbejde inden for biologi, botanik, zoologi og beslægtede områder

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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