stillingsbetegnelse: Quality Assurance of newly built Tablet Facility

jobbeskrivelse:
Research & Development Denmark - Måløv Do you want to be part of the team assuring the quality of one of our new tablet production facilities? Novo Nordisk has built a new factory in Måløv which will be part of setting new standards for diabetes treatment. To succeed with this ambition we need people with a pioneer spirit, that have high engagement and that thrive in a constant changing environment. About the department Oral Drug Product (DP) Launch Plant Quality Assurance (QA) is a newly established department, which will employ approximately 15 skilled and motivated colleagues, who work with assuring quality and compliance of the facility, the equipment as well as the quality management system. The position In close cooperation with your colleagues in QA, you act as a QA for the facility and the quality management system. You contribute to finding solutions for ad hoc questions and challenges within compliance of cGMP facilities. The job is related to daily operation and qualification/validation of equipment and facilities for oral DP manufacture. You will assure that the documentation for implementation and maintenance of equipment is compliant with internal and external requirements. Furthermore, you will approve facility related documentation needed for the operation of the plant such as change requests, Non-Conformities (NC), Standard Operating Procedures (SOP’s), as well as trend reports for environmental monitoring and utilities. 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's in Pharmacy, Chemical Engineering or corresponding qualifications and at least some years of experience within the pharmaceutical industry. You have knowledge within some of the following areas: GMP, validation/qualification, analytical equipment for In Process Controls (IPC), equipment used in pharmaceutical 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. Working at Novo Nordisk 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 11 September 2016.

Arbejdsgiver Navn: NOVO NORDISK A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Ingeniørarbejde inden for kemi

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark