Arbejde QA Senior Project Manager Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: QA Senior Project Manager

jobbeskrivelse:
- Project Management - Denmark - Bagsværd Do you want to work with inspections and cross-functional tasks within Biopharm QA? Biopharm QA Compliance and QMS is looking for a Senior Project Manager who can coordinate the preparation and support to Health Authorities inspections in Biopharm as well as managing cross-functional quality projects. About the department Biopharm QA Compliance and QMS is part of the Biopharm QA organisation and consists of 9 highly qualified professionals and specialist. The department is located in Bagsværd, but we work across functions and sites and therefore our employees covers activities which are performed at the different Danish Biopharm sites (Gentofte, Måløv, Kirke Værløse, Hillerød and Kalundborg). Our main responsibility is to ensure the inspection readiness and adherence to QMS, quality processes and process governance, compliance, quality improvements projects, as well as customized GMP training. The job One of your main responsibilities will be to plan, prepare and execute the inspections by Health Authorities in Biopharm in collaboration with involved LoB and QA departments; The planning consists of holding meetings to provide involved departments within and outside Biopharm with relevant information about the inspection; You will be also responsible for ensuring that the necessary preparation activities are taking place and you will be managing the inspection process together with the secretariat team; You will share this responsibility with an experienced colleague with whom you will collaborate daily in order to optimally ensure continuous support to inspections. Furthermore, you will be regularly assigned cross-functional Quality projects as well as improvement initiatives. You will be working closely with Biopharm Quality management and PSQ support functions. We can offer you an interesting position with good opportunities for both professional and personal development. Qualifications You have a Master degree in pharmacy, engineering or natural science and you are familiar with GMP requirements for the pharmaceutical industry. You have minimum 3 years of relevant practical experience, including working with quality assurance activities, GMP inspections and managing cross-functional projects. You are a team player, and also demonstrate ability to work independently; you take charge, and also ensure stakeholder involvement and confidence throughout. You create structure and overview, have a keen eye on details and are an example of a strong quality culture. As a person, you are ambitious and outgoing with a proactive approach. You have good co-operation skills and are able to communicate on different levels in the organisation and with external stakeholders. At Novo Nordisk, we use our skills, dedication and ambition to help people with diabetes. We offer the chance to be part of a truly global work place, where passion and engagement are met with opportunities for professional and personal development. Contact Please contact Cristina De Simoni Klitgaard at +45 3075 6783. Deadline 29 January 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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