Arbejde IT Quality Assurance of new Tablet & Packaging Facility Hovedstaden Novo Nordisk A/S - jobtilbud

GÆLDER
stillingsbetegnelse:
IT Quality Assurance of new Tablet & Packaging Facility

jobbeskrivelse:
- Research & Development - Denmark - Måløv Do you want to be part of the team establishing a new tablet and packaging facility? Novo Nordisk has initiated a project to build a new factory in Måløv which will be supplying the market with tablets and thus set new standards for diabetes treatment. To succeed with this ambitious project we need people with a pioneer spirit who like to build something completely new, that have high engagement and that thrive in a constant changing environment. About the department We’re in the process of establishing a new QA department as part of the project organisation. In Oral DP Launch Plant QA we ensure quality and compliance of the facility, the equipment as well as the quality management system. The job In close cooperation with your colleagues in QA, you act as a QA for project team establishing the new facility. You contribute to finding solutions for ad hoc questions and challenges within compliance of GMP facilities. The job is related to qualification/validation of IT and Automation solutions for oral drug product manufacture and packaging. Your main task will be assure that the documentation for implementation and maintenance of IT & Automation systems are compliant with internal and external requirements. Furthermore, you will assist your colleagues in getting the qualification documentation for equipment & facility approved as well as approving facility related documentation needed for the operation of the plant such as change requests, non-conformities and SOP’s. Our continuing high level of audit and inspection readiness is on top on your agenda. This means that in QA we work with QA oversight where you proactive, together with your colleagues, will identify areas where our compliance can be strengthened. You have a risk based approach to the manufacturing process and product, and you contribute to find the right balance between patient safety, compliance to requirements and effective business conduct. Qualifications Ideally, you have a master in Pharmacy, Chemical Eng. or corresponding qualifications and at least 3 years of experience within the pharmaceutical industry. You have thorough knowledge within qualification of IT and automation solutions as well as within some of the following areas: GMP, validation/qualification, equipment used in tablet or aseptic production. You enjoy working in a dynamic environment, where teamwork is at the top of the agenda. Also, you are quite adaptable and challenge our way of doing things, so that we will get even better. You focus on results and quality – and contribute to the right level of compliance. 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 Peter Søtofte Elten at +45 3079 8453 or Peter Langkilde Sonne at +45 3079 8415. Deadline 4 March 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

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