stillingsbetegnelse: Labelling Supporter in RA Affiliate Coordination

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. 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. For the Labelling Support team, part of RA Affiliate Coordination in Regulatory Operations in Søborg, we are looking for a Labelling Supporter for a temporary position. About the department RA Affiliate Coordination is a department in Regulatory Operations (part of Regulatory Affairs). Regulatory Affairs is a fast-changing field, and the 450 employees serve as Novo Nordisk’s advocates around the world – and make a meaningful difference to our business making medicine available to patients all over the world by ensuring rapid regulatory approval in all markets. In Labelling Support we are responsible for approval of master data and support related to labelling and packaging materials for all Novo Nordisk A/S products and devices worldwide. You will be reporting to the team leader of the Labelling Support team and will be part of a team consisting of 7 labelling supporters situated in Søborg, Denmark. The team works closely with especially logistics in Product Supply, other teams in Regulatory Affairs and Affiliates all over the world. The job You will primarily be involved in pre-approval of master data for packaging material and master packing orders for Novo Nordisk A/S products and devices for production sites using the production model PRISM. The team works, among others, closely together with QA from both R&D and Product Supply, logistics at all NN production sites, Regulatory Affairs Affiliates worldwide and Regulatory Affairs HQ. You will therefore also be involved in general support to our stakeholders ensuring good collaboration related to our core competencies. We work in a fast-paced environment with changing deadlines and tasks ensuring a challenging and interesting job. Qualifications We are looking for a candidate who can work independently and systematically with an eye for details. In addition, you are used to work with tight deadlines and changing assignments. Experience from master data entry and approval and/or the pharmaceutical industry together with GMP knowledge will be considered an advantage. As stakeholder management is an important part of the job, we expect you to have good communication skills and expect that you possess strong cross-cultural skills. Finally, you must be 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 Louise Wanning Tvede Anderson on +45 3079 1551. Deadline 16 January 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