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Trabajar en Dinamarca (HOVEDSTADEN) de Ingenieros

Experienced Quality Specialist

Clasificación del trabajo: Profesionales científicos e intelectuales : Profesionales de las ciencias y de la ingeniería : Ingenieros (excluyendo electrotecnólogos) : Ingenieros no clasificados bajo otros epígrafes.
Arbejde, der forudsætter viden på højeste niveau inden for pågældende område : Arbejde inden for naturvidenskab og ingeniørvirksomhed : Ingeniørarbejde (undtagen inden for elektroteknologi) : Andet ingeniørarbejde (undtagen elektroteknologi).

Descripción de la oferta de trabajo:

Do you want to be a member of a team that ensures that Oticon complies with the ISO 13485:2016, MDSAP and FDA CFR 21 part 820? Do you enjoy performing internal audits and know the requirements towards document control? Is collaboration one of the most important aspects for you? Then perhaps you are the new quality specialist we are looking for.


Oticon – a big, complex organization, with the purpose to change the life for people with a hearing loss


Oticon strives to be the leader in high performance hearing solutions and to supply the most sophisticated technology and audiology possible. We have a relentless drive for innovation and is in the absolute forefront of technology, which improves the lives of people with hearing loss.


Oticon is certified after ISO 13485:2012 and complies within the requirement in FDA CFR 21 part 820. Early in 2018, we will be certified after ISO 13485:2016 and MDSAP. We have a continually focus on being in compliance also with the local requirements.


The workplace for this position is at Kongebakken in Smørum, Denmark. We are around 13.000 people worldwide, and you will be cooperating with people from several places around the world.

In the QA department we are in total 13 people, eight placed in Denmark and five placed in Poland. The QA department is responsible for the Quality Management System (QMS) and some of the key QA processes and tools e.g. internal audit and calibration. The QMS covers several sites and departments.


Qualifications - communications and cooperation

You are engineer or have similar education and have 5-10 years of QA experience in the medical device industry. You should have experience with at least ISO 9001/ISO 13485, Medical Device Directive (MDD) and FDA CFR 21 part 820, have conducted internal audits and project management.

It is important that you can transform the requirement into guidelines for both R&D, Sales & Marketing and Production. Furthermore, you need to be able to cooperate about the implementation. So, knowing the requirements toward medical devices and being able to find and implement the solutions in the rest of the organization, is the best qualification you can have.


How to apply:

Please send your CV and application as soon as possible and no later than October 30th 2017. Please notice we will only consider candidates using the electronic recruitment system.

If you want more information about the position, please contact Mette B. Dyhrberg at medyReemplazar por una or mobile +45 20630183.

Servicio de empleo de origen: AMS, Servicios Públicos de Empleo, Dinamarca.

País del trabajo: Dinamarca.

Región: Hovedstaden.

Ver 1096 ofertas de trabajo en "HOVEDSTADEN" (Dinamarca).

Fecha de inicio: 18/10/2017.

Nº de vacantes: 1.

Nivel educativo requerido: Sin especificar.

Tipo de contrato: Jornada completa.

Duración del contrato: Indefinido.

Cómo solicitar el puesto:
Mette B. Dyhrberg

Empresa: OTICON A/S.

Contacto: Karoline Bertelsen Rønje

Ver las 238 ofertas de trabajo de Profesionales científicos e intelectuales : Profesionales de las ciencias y de la ingeniería : Ingenieros (excluyendo electrotecnólogos) : Ingenieros no clasificados bajo otros epígrafes ofertadas.

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