Arbejde Associate Manager to QC support team in Material Manufacturing Develop Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse:
Associate Manager to QC support team in Material Manufacturing Develop

jobbeskrivelse:
- Management - Denmark - Hillerød Do you like challenges and do you have a strong track record leading your team members to success? Do you have experience with Quality Control (QC) Support? If so, this job as associate manger in a newly established department called Material Manufacturing Development (ManDev) in Hillerød could very well be your new job. About the department You will join Material ManDev in Product Supply, Sourcing Operations, which will consist of 34 employees organised in three teams, two QC support teams and one material transfer team, when we are fully manned. We will be located in Hillerød from November 2015. We are responsible for coordinating transfer of raw materials incl QC methods from development to production, preparing registration documentation and maintain documentation on existing raw materials. We will be cooperating with a variety of functions, including development, QC and QA for raw materials, and various Novo Nordisk production sites and external contract manufactures. The job As associated manager for one of the QC Support teams you will be responsible for ensuring timely transfer of QC methods from development to production in close collaboration with both development and final QC laboratory. The team will be responsible for establishment of new QC platforms, qualification of equipment and validation of new methods and will furthermore be involved in optimization of existing QC methods. As we are a newly established department, within a new area and with only one QC support team, you can expect to get high influence on setting the right team and for creating a work environment that fosters job enthusiasm and a can-do attitude. You will be an important key player for ensuring that you and your team, in close collaboration with our stakeholders, create standard processes for the different activities. You will get responsibility for the team’s performance and for ensuring that the activities are planned and timely completed and in compliance with GMP and corporate standards. You continuously follow up on the team’s performance and manage board meetings to provide a complete overview of activities. Qualifications You have a solid education in science, supplemented with experience from QC or QC support. Preferable you will also have experience with drug development. Naturally, you take an interest in people management, and you know the value of earning trust and respect from colleagues, and in addition, you have experience with change management. You have a structured approach to your work and are capable of keeping a sense of perspective. You have to be a person who thrives in a busy and constantly changing workday. You also need to be capable of contributing with ideas for optimising procedures. You are fluent in both spoken and written 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 contact Trine Kantsø +45 3079 4362. Deadline 30 November 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

GÆLDER

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