stillingsbetegnelse: Quality Coordinator

jobbeskrivelse:
- Quality - Denmark - Bagsværd Are you looking for an opportunity to apply your knowledge about and experience within GxP requirements, quality and compliance in an engaged and proactive way? Do you enjoy maintaining the balance between having the overview and knowing the detail? Do you excel when it comes to stakeholder management and sparring with other professionals? Then you may be our new Quality and GMP-coordinator for Contract and Local Manufacturing (CLM) in Bagsværd. About the department Contract and Local Manufacturing (CLM) is responsible for all Novo Nordisk contracts and licence manufacturing of semi-finished and finished drug products to local and global markets. CLM comprises of around 280 employees with 40 based in Denmark, 120 in Kaluga Russia and 120 in Koriyama Japan. Our main office is located in Bagsværd, Denmark, which will also be your main location. The Job As our Quality and GMP coordinator, you will be the overall Quality Ambassador of CLM. You are involved in setting quality targets for the Danish as well as the organisations outside Denmark to ensure CLM as a Unit is in control of our Quality and Compliance. You will be responsible for ensuring the general level of quality and compliance is continuously improved and that our quality systems and –processes live up to the requirements of relevant authorities and Novo Nordisk standards. You will therefore also play the most central part when inspections and audits are conducted in the area and in the departments. A significant task for the Quality and GMP-coordinator will be to follow-up and continuously improve the quality and compliance of all areas in CLM. You will therefore also be expected to develop and implement best practices as well as teaching and guiding your colleagues about rules, regulations, systems and processes. The position as Quality and GMP-coordinator is a newly established position. You will be reporting directly to Lars Bisgaard, who is the Corporate Vice President of CLM. You will be responsible for acting as the liaison between the line-of-business of CLM and the quality department, and therefore to be able to understand and convey messages and perceptions from both areas and proactively identify solutions that meets the requirements. Qualifications You hold a relevant academic degree (e.g. Pharmacy, Engineering or Chemistry) and have extensive experience from working within the pharmaceutical industry with GxP, quality and compliance requirements. You keep yourself updated continuously on changes in authorities’ requirements, and have an excellent ability to translate these into relevant targets as well as engaging with stakeholders to implement these targets. You have great interpersonal, stakeholder and communication skills, and an ability to set a clear direction and inspire others to follow. You have a strong personal drive enabling you to persistently pursue your goals and achieve results in a challenging environment. Lastly, you are proficient both in spoken and written English. At Novo Nordisk, you will have the opportunity to build a life-changing career in a global business environment. From research and development, to manufacturing, marketing and sales, we strive to improve quality of life for more than 371 million people living with diabetes. Contact For further information, please contact Lars Bisgaard at +45 3075 9318. Deadline 9 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