stillingsbetegnelse: QA Professional

jobbeskrivelse:
- Quality - Denmark - Hillerød Are you ready to use your expertise in ensuring high quality work within the medical device area of Novo Nordisk? If so there is a challenging and exciting position in DMS Process QA. About the Department Device Manufacturing Sourcing (DMS) is a production organisation located near Copenhagen. Our challenge is to mould, preassemble and produce high quality components and bring them fast to market. You will be part of our DMS Process QA department in Hillerød where we are 10 engaged and innovative colleagues who strive for a good collegial and professional atmosphere. The job As QA Professional you are responsible for the quality of our components, including approval of validation documentation, change requests and instructions among other tasks. You will be working in cooperation with competent and experienced colleagues. You are furthermore participating in QA related projects. One of your primary objects is to perform review and approval of validation documents in due time and in full compliance with the GMP standards. Good relations and communication skills are key tools when handling the quality issues in the best possible way. Quality is the key word in this job and therefore it is natural for you to have an on-going dialogue with your partners regarding how to ensure quality and compliance. As QA Professional quality has your concern, which means that you can stand firm when needed in considerations of patient safety and regulatory requirements. Look forward to have an exciting job, where you have a high degree of responsibility. We offer this challenging position in a dynamic environment where you have good opportunities for personal and professional development. Qualifications You hold a master degree in engineering within mechanics/machines/plastics or similar academic education. Preferably your academic background is supplemented with experience from the pharmaceutical industry and/or knowledge regarding moulding and assembly processes. Based on your experiences within the field, you are used to work with GMP and the regulations relevant for medical devices. Furthermore it is relevant that you are interested in IT processes. You work systematically and are able to make a perspective view, and you are comfortable with taking decisions. You have a strong quality mindset, and are able to prioritise several tasks in a changing environment. Precise communication is essential and you must be capable of taking part in a constructive cooperation concerning the various tasks. On a personnel level you are known for your positivity, flexibility and persistence. 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 Lene Cletus Petersen on + 45 3079 0412. Deadline 10 January 2016.

Arbejdsgiver Navn: Novo Nordisk A/S

Arbejdsgiver telefonnummer: 44448888

Arbejdsgiver faxnummer: 44442314

Job kort beskrivelse: Ingeniørarbejde i industri og produktion

land: Danmark

region: Hovedstaden

Kontrakt varighed: Fast

Kontrakttype: Fuldtid

krævede uddannelse: Ikke angivet

Kilde til jobtilbud: AMS, Offentlige arbejdsformidlinger, Danmark