Arbejde CVP Quality Coordinator Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: CVP 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 from different back-grounds? Then you might be the new CVP Quality Coordinator for Contract and Local Manufacturing (CLM). About the department CLM is part of Novo Nordisk’s Product Supply organisation, responsible for Novo Nordisk’s outsourced drug manufacturing world-wide. The primary role of CLM is to establish and manage production handled by local manufactures in countries like India, Bangladesh, Algeria, Egypt, Russia, Japan and several European countries. Your role will cover support to the CLM department in Denmark (Bagsværd) as well as the sites in Japan & Russia. You should expect to visit the sites 1-2 times per year. The Job As CVP Quality Coordinator you will be the Quality Ambassador of CLM. You will play a key role in setting quality targets for Denmark, Japan & Russia and facilitate and communicate a close follow up. You will be responsible for the continuous improvement of the general level of quality and compliance in CLM as well as ensuring that quality systems and –processes live up to the requirements of relevant authorities and Novo Nordisk standards. You are expected to develop and implement best practices while teaching and guiding your colleagues about rules, regulations, systems and processes. You will also be an anchor person when inspections and audits are conducted. Organisationally you will be part of CLM’s Business Support department which consists of 8 dedicated colleagues and you will also enter D&S Quality Coordinator network. You will work closely with the management team in CLM and be responsible for acting as the liaison between the line-of-business and the Quality Assurance department in CLM. This will require the ability to understand and convey messages and perceptions from both areas and proactively identify solutions to meets 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 guide the organisation based on your knowledge. Experience with Quality Management Reviews, Quality Activity Planning, Quality data systems and Audit and Inspection preparation and coordination may also offer a smooth entry into the job. Basic knowledge of MS-Excel is an advantage. As a person you are structured, data-driven, analytical and a clear communicator. You manage to have an overview and set direction while keeping an eye on the detail. You work independently 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 366 million people living with diabetes. Contact For further information, please contact Katrine Bisgaard Høy at +45 3079 2715. Deadline 19 February 2016.

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

GÆLDER

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