stillingsbetegnelse:
Regulatory Associate in Faster Acting Insulin Projects

jobbeskrivelse:
- Regulatory Affairs - 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 is seeking Regulatory Associate for our department Regulatory Faster Acting Insulins Projects. If you thrive in a dynamic and challenging environment with focus on regulatory execution, this job offers you the opportunity to be part of the major regulatory submissions. About the department Novo Nordisk Regulatory Affairs makes medicine available to patients all over the world by ensuring rapid regulatory approvals in all our markets. Regulatory Affairs is a fast-changing and complex landscape, therefore, a high level of professionalism and a thorough business understanding is essential for the employees in our unit in order to make a difference to our business. We are currently looking for a Regulatory Associate with an interest in administrative tasks within late stage development project heading toward regulatory submission. The job In our team you will work in a fast-paced environment with tight deadlines, cross-departmental collaboration and the challenges of international communication. .You main responsibility will be mangment and compilation of regulatory documents, as well as preparation of patient information leaflet and label for regulatory submission. You will also be involved in administration and coordination of a wide range of regulatory tasks to ensure a smooth workflow in our department – but also among our stakeholders within Novo Nordisk headquarters and affiliates. You will work together with dedicated and highly engaged professionals developing and executing regulatory strategies with the aim to make innovative medicines available for patients with diabetes Qualifications You may have an education within the healthcare area (e.g. Pharmacy Technician, Nurse or Laboratory Technician) as well as experience from working in regulatory affairs. You have a flair for IT systems and are comfortable using English in your daily work. On a personal level, you are proactive, flexible, systematic and have a strong quality mindset and a sense for details. As our project is entering regulatory execution phase, it is crutial that you thrive in a busy environment with overalping and changing deadlines, have good coordination and planning skills and maintain a healthy sense of humour especially when the pressure is on. Your are a strong team player, but also enjoy working independently. At Novo Nordisk, we work together to prevent, treat and eventually cure diabetes. Nearly 371 million people worldwide are living with diabetes today, with two people diagnosed with the disease every ten seconds. Working here is not just a way to make a living, but a way to make a difference Contact For further information, please call Magdalena Niepsuj Jayatissa on +45 3079 3647. Deadline 8 December 2014.

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