stillingsbetegnelse: QA Professional, temporary position

jobbeskrivelse:
•Quality •Denmark - Måløv Do you see yourself contributing to high quality and compliance of products used for Novo Nordisk clinical trials globally? Then here is an opportunity to start or continue your career at Novo Nordisk A/S with a 12 month temporary position as QA Professional. About the department You will be part of a dedicated team of 22 colleagues located in Måløv. We are part of the CMC Quality Assurance organization, which is responsible for all QA activities related to Investigational Medicinal Products used for the increasing number of Novo Nordisk clinical trials globally. We are looking for a new colleague to support the quality activities in the clinical supplies part of the Novo Nordisk R&D organisation. The job The organisation’s continued high level of compliance, audit and inspection readiness is at the top of your agenda. As a Qualified Person delegate you will certify final packed products for use in clinical trials worldwide. You will be responsible for quality assurance of activities and documents related to the labelling, packaging and supply of products for Novo Nordisk trials globally. You will provide quality support where your ability to apply Novo Nordisk and authority regulations and requirements is key to solving challenges both in the daily operation and the long term development of the business and its quality system. You will interact with colleagues across the CMC Supply organisation and also with colleagues from other parts of Novo Nordisk A/S both in Denmark but also with affiliates worldwide. You can look forward to entering into an energetic and positive working environment where co-operation amongst highly engaged and dedicated Novo Nordisk colleagues is key to yours and the company’s success. Qualifications You hold an academic degree as pharmacist. To be considered for the position you must have a minimum 1 year’s experience working according to GMP requirements (production/QA) in a pharmaceutical business with a manufacturing authorization from DHMA (§39). On a personal level, you demonstrate engagement, credibility and empowerment. You are a positive and open minded team player who can co-operate at all organizational levels. You like a professional and dynamic environment with many simultaneous tasks and changing priorities. You are a skilled communicator, and you thrive on unfolding your high level of energy and spirit in an international, dynamic environment. Feel free to submit your job application in either English or Danish, whichever you prefer. Also please share this add with friends and professional connections you might think would be interested in pursuing a career opportunity at Novo Nordisk. In Novo Nordisk it is your skills, your commitment and your ambitions, which help us to improve many people's lives. In return we offer you the opportunity to work with exceptionally talented colleagues and we offer you a wide range of opportunities for professional and personal development. Contact For further information please call Birthe Boldvig Rottwitt on +45 3075 0158. Deadline 1 July 2014.

Arbejdsgiver Navn: NOVO NORDISK A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Farmaceutarbejde

land: Danmark

region: Hovedstaden

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark