Arbejde Analysis Coordinator for Material ManDev Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse: Analysis Coordinator for Material ManDev

jobbeskrivelse:
- Project Management - Denmark - Hillerød Do you want take part in coordinating the implementation of analytical methods on complex raw materials and Support QC with analytical challenges? In that case you should apply for the new position as Analysis Coordinator in Material MDev. If you are as ambitious as we are, you can look forward to an exciting job in an environment where we seek to be best in class in everything we do. About the department You will join a newly established Material Manufacturing Development (Material MDev) department in Product Supply Sourcing Operations that will consist of 30 employees organised in three teams. We will be located in Hillerød from November 2015. We are responsible for coordinating transfer of raw materials from development to production 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 You will be responsible for coordinating the analytical development and validation activities from clinical phase 3 to launch on raw materials needed for our new products being transferred from development. Your primary focus will be on analytical activities related to complex raw materials produced at external contract manufactures (CMO). You will be the CMOs primary contact regarding coordinating analytical activities to ensure that the CMO has needed analyses ready to support delivery of the needed material. You will work closely with the drug substance and drug product coordinators across the organisation. You will also have a close cooperation with the chemists in the department to secure timely implementation of new materials and new analytical methods in Novo Nordisk. A broad understanding of analytical methods is needed and a high GMP and compliance mind-set is required. In general, the assignments carried out by the department are diverse as we deliver to various parts of Novo Nordisk. This gives a variety of analytical challenges and strong collaboration with your colleagues is therefore an essential key to success. Qualifications You hold a master degree in Chemistry, Pharmacy, Engineering or another relevant field within the natural sciences. Your degree is supplemented with several years of experience with analytical methods and in-depth knowledge of working with GMP in a laboratory environment. Strong project management skills are required. You have a high level of energy to drive yourself and your colleagues forward. You are result-oriented and take pride in delivering on your milestones, and you motivate your colleagues with a positive, forthcoming attitude. You work well independently, although it also motivates you to cooperate with colleagues and stakeholders across functions and departments. Lastly, you must have fluency in written and spoken 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 Bodil Rindel at +45 3079 4379 or Tine Sloth Høg at +45 3075 0019. 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

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