stillingsbetegnelse: Regulatory Professional

jobbeskrivelse:
- Regulatory Affairs - Denmark - Søborg In Regulatory Affiliate Support, we are looking for a Regulatory Professional with excellent IT skills to join a dedicated group of people working closely together with Novo Nordisk A/S affiliates worldwide, Regulatory Affairs product/project groups in headquarters in Denmark and with the Regulatory Affairs Operations Team in India. About the department Regulatory Affiliate Support is part of Regulatory Operations within Regulatory Affairs, which makes medicine available to patients all over the world by ensuring rapid regulatory approval in all markets. Regulatory Affairs is a fast-changing field, and the 330 employees serve as Novo Nordisk’s advocates around the world – and make a meaningful difference to our business. You will be part of a dedicated team consisting of 15 people situated in Søborg, Denmark providing support and services across Novo Nordisk A/S projects and products. The job In Regulatory Affiliate Support we are responsible for supplying Novo Nordisk A/S affiliates with additional registration file documentation for submissions to health authorities worldwide. Furthermore, we are responsible for management of the IT system Register to ensure precise updates of our product portfolio in collaboration with the Regulatory Operations Team in India. As Regulatory Professional, you will be working with updating and maintaining data in Register as well as optimizing processes related to the system and for documenting the process. In addition, collaboration with Novo Nordisk A/S affiliates supporting these with additional documentation and samples will be part of your job. Supporting various stakeholders such as Product Supply, Quality and Regulatory Affairs with knowledge within Register and requlatory issues will also belong under your responsibility. New requirements and challenges constantly emerge within these areas; therefore, the position includes possibility for project work to identify optimisations and solutions. Qualifications You have a relevant degree within science/pharmacy/medicine or business/marketing with advanced IT skills, preferably witin Register or similar systems, as well as a strong business and process orientation. You have at least 3 years experience from the pharmaceutical industry and within regulatory affairs. We expect that you are able to drive activities and tasks independently and systematically with an eye for detail and high quality output. You are able to stay on target, work with tight deadlines and manage multiple assignments without loosing track. You have good analytical skills and problem solving abilities and address your responsibilities with decisiveness and a positive mind set. You have advanced communication skills and have the experience with presenting in large forums as stakeholder management and communication are essential for succeeding in the job. Furthermore, we expect that you possess strong cross-cultural skills and are used to working with international business partners. Finally, you must be fluent in written and spoken English. In Novo Nordisk A/S it is your skills, your commitment and your ambitions which help us to improve many people’s lives. In return we offer you the opportunity to work with talented colleagues, and we offer you a wide range of opportunities for professional and personal development. Contact For further information, please contact Pil Arnild Mortensen at +45 3079 0635 or Tina Lindquist at +45 3075 9652. Deadline 4 August 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