medical device auditor in arnhem

toegevoegd
dienstverband
tijdelijk
solliciteer nu

vacature details

toegevoegd
standplaats
arnhem, gelderland
vakgebied
Techniek
dienstverband
tijdelijk
werktijden
40
ervaring
5
referentie
IGB207435487
solliciteer nu

functieomschrijving

You are responsible for the assessment of technical files and the auditing of the quality system of your customers (from high innovative start-ups to large multinationals, both national and international).
You act as a linchpin and maintain frequent contact with your customers, colleagues, external experts like physicians, contractors and authorities.
You will have the opportunity to represent DEKRA at conferences.
The position entails travelling within and outside Europe, approximately 20-30% of the time.

Arbeidsvoorwaarden
.Extentional internal training, challenging environment, competitive salary and benefits.

vaardigheden

Requirements:
Higher vocational or university level education, in life and/or engineering sciences.
A minimum of 5 years of full time work experience in medical device related industry, including at least 2 years in R&D, QA/RA.
Experienced in at least one of the following devices categories and areas of expertise: Active medical devices, Active implantable medical devices, soft tissue implants, cardiovascular devices, drug device combinations, animal tissue and In Vitro Diagnostics.
Experience with quality management systems and relevant laws and regulations, at least CE.
 Project management and auditing experience is considered an advantage.

functie-eisen

WO