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Traduction de «kwaliteitsmanager in de industrie » (Néerlandais → Anglais) :

TERMINOLOGIE
voir aussi les traductions en contexte ci-dessous

kwaliteitscoördinatrice in de industrie | kwaliteitsmanager procesindustrie | kwaliteitscoördinator in de industrie | kwaliteitsmanager in de industrie

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

industrial quality control technologist | industrial quality control testing supervisor | engineering and quality control manager | industrial quality manager

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]

manager dienstverleningskwaliteit | manager kwaliteit dienstverlening | kwaliteitsmanager | kwaliteitsmanager dienstverlening

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

quality control services manager | quality service supervisor | quality assurance coordinator | quality services manager

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]

baas kwaliteits- en controledienst schoenproductie | kwaliteitscontroleur schoenproductie | kwaliteitsmanager schoenindustrie | kwaliteitsmanager schoenproductie

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

footwear quality assurance manager | footwear quality coordinator | footwear quality executive | footwear quality manager

https://ec.europa.eu/esco/port (...) (...) [HTML] [2017-12-31]

https://ec.europa.eu/esco/port (...) [HTML] [2017-12-31]

ingenieur olie-industrie

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

Oil well engineer

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

procesoperator in petrochemische industrie

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

Chemical/gas/petrol processor

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

procesoperator in keramische industrie

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

Ceramics processor

https://browser.ihtsdotools.or (...) (...) [HTML] [2018-01-01]

https://browser.ihtsdotools.or (...) [HTML] [2018-01-01]

industrie van luxeartikelen [ industrie van luxe-artikelen | luxeprodukt ]

http://eurovoc.europa.eu/drupa (...) (...) [HTML] [2017-12-31]

luxury products industry [ luxury product ]

http://eurovoc.europa.eu/drupa (...) (...) [HTML] [2017-12-31]

http://eurovoc.europa.eu/drupa (...) [HTML] [2017-12-31]

bio-industrie [ biogebaseerde industrie | industrie op biobasis ]

http://eurovoc.europa.eu/drupa (...) (...) [HTML] [2017-12-31]

bio-industry [ bio-based industry | biotechnology-based industry | biotechnology industry ]

http://eurovoc.europa.eu/drupa (...) (...) [HTML] [2017-12-31]

http://eurovoc.europa.eu/drupa (...) [HTML] [2017-12-31]

optische industrie [ bril | contactlens | optisch glas | precisieoptica ]

http://eurovoc.europa.eu/drupa (...) (...) [HTML] [2017-12-31]

optical industry [ contact lens | precision optics | spectacle lens | spectacles | Optical product(STW) ]

http://eurovoc.europa.eu/drupa (...) (...) [HTML] [2017-12-31]

http://eurovoc.europa.eu/drupa (...) [HTML] [2017-12-31]

bio-based industrie | biogebaseerde industrie | industrie op biobasis

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

bio-based industry

http://iate.europa.eu/FindTerm (...) (...) [HTML] [2017-12-31]

http://iate.europa.eu/FindTerm (...) [HTML] [2017-12-31]

TRADUCTIONS EN CONTEXTE

- vier jaar beroepservaring op het gebied van gezondheidsproducten of in aanverwante sectoren (bv. industrie, audit, gezondheidszorg, onderzoekervaring), waarvan twee jaar op het gebied van kwaliteitsmanagement;

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

four years professional experience in the field of healthcare products or related sectors (e.g. industry, audit, healthcare, research experience) whilst two years of this experience shall be in the area of quality management

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

http://www.europarl.europa.eu/ (...) [HTML] [2013-10-21]

– vier jaar beroepservaring op het gebied van gezondheidsproducten of in aanverwante sectoren (bv. industrie, audit, gezondheidszorg, onderzoekervaring), waarvan twee jaar op het gebied van kwaliteitsmanagement;

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

- four years professional experience in the field of healthcare products or related sectors (e.g. industry, audit, healthcare, research experience) whilst two years of this experience shall be in the area of quality management

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

http://www.europarl.europa.eu/ (...) [HTML] [2013-10-21]

1. De aangemelde instanties moeten voldoen aan de organisatorische en algemene voorschriften en de voorschriften inzake kwaliteitsmanagement, middelen en processen die nodig zijn om de taken te verrichten waarvoor zij overeenkomstig deze verordening zijn aangewezen.

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

1. Notified bodies shall satisfy the organisational and general requirements and the quality management, resource and process requirements that are necessary to fulfil their tasks for which they are designated in accordance with this Regulation.

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

http://www.europarl.europa.eu/ (...) [HTML] [2013-10-21]

(19) Gezien het belang van normalisatie en traceerbaarheid op het gebied van medische hulpmiddelen moet de naleving van geharmoniseerde normen zoals omschreven in Verordening (EU) nr. 1025/2012 van het Europees Parlement en de Raad 1 fabrikanten de mogelijkheid bieden om de conformiteit met de algemene veiligheids-, prestatie- en andere wettelijke voorschriften, zoals kwaliteitsmanagement en risicobeheer, aan te tonen.

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

(19) To recognise the important role of standardisation and traceability in the field of medical devices, compliance with harmonised standards as defined in Regulation (EU) No 1025/2012 of the European Parliament and of the Council 1 should be a means for manufacturers to demonstrate conformity with the general safety and performance requirements and other legal requirements, such as quality and risk management.

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

http://www.europarl.europa.eu/ (...) [HTML] [2013-10-21]

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(19) Gezien het belang van normalisatie op het gebied van medische hulpmiddelen moet de naleving van geharmoniseerde normen zoals omschreven in Verordening (EU) nr. [./.] betreffende Europese normalisatie fabrikanten de mogelijkheid bieden om de conformiteit met de algemene veiligheids-, prestatie- en andere wettelijke voorschriften, zoals kwaliteitsmanagement en risicobeheer, aan te tonen.

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

(19) To recognise the important role of standardisation in the field of medical devices, compliance with harmonised standards as defined in Regulation (EU) No [./.] on European standardisation should be a means for manufacturers to demonstrate conformity with the general safety and performance requirements and other legal requirements, such as quality and risk management.

http://www.europarl.europa.eu/ (...) (...) [HTML] [2013-10-21]

http://www.europarl.europa.eu/ (...) [HTML] [2013-10-21]

[24] Standpunten van onder meer BDI (Bundesverband der Deutschen Industrie), DIHK (Deutscher Industrie‑ und Handelskammertag), CBI (Confederation of British Industries), CCIP (Chambre de commerce et d'industrie de Paris), CGPME (Confédération générale des petites et moyennes entreprises), Unioncamere, DigitalEurope, Orgalime, ACT (Association for Competitive Technology), Cefic.

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2010-11-09]

[24] Position papers from BDI (Bundesverband der Deutschen Industrie), DIHK (Deutscher Industrie- und Handelskammertag), CBI (Confederation of British Industries), CCIP (Chambre de commerce et d'industrie de Paris), CGPME (Confédération générale des petites et moyennes entreprises), Unioncamere, DigitalEurope, Orgalime, ACT (Association for Competitive Technology), Cefic and others.

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2010-11-09]

http://eur-lex.europa.eu/legal (...) [HTML] [2010-11-09]

[24] Standpunten van onder meer het BDI (Bundesverband der Deutschen Industrie), DIHK (Deutscher Industrie- und Handelskammertag), CBI (Confederation of British Industries), CCIP (Chambre de commerce et d'industrie de Paris), CGPME (Confédération générale des petites et moyennes entreprises), Unioncamere, DigitalEurope, Orgalime, ACT (Association for Competitive Technology), Cefic.

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2010-11-09]

http://eur-lex.europa.eu/legal (...) [HTML] [2010-11-09]

Het Europees referentiekader voor kwaliteitsborging in beroepsonderwijs en -opleiding is bedoeld om het kwaliteitsmanagement op dit gebied op nationaal niveau te verbeteren door middel van een aantal gemeenschappelijke criteria en indicatoren.

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2009-06-17]

The European Quality Assurance Reference Framework for VET is designed to improve quality management practices at national level within this field by means of a set of common criteria and indicators.

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2009-06-17]

http://eur-lex.europa.eu/legal (...) [HTML] [2009-06-17]

bevordering van kwaliteitsmanagement en goede dienstverlening en faciliteiten op infrastructureel gebied in de visumaanvraagprocedure;

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2007-05-22]

promotion of quality management, and good services and facilities in terms of infrastructure in the visa application process;

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2007-05-22]

http://eur-lex.europa.eu/legal (...) [HTML] [2007-05-22]

[3] [http ...]

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2000-12-31]

[3] [http ...]

http://eur-lex.europa.eu/legal (...) (...) [HTML] [2000-12-31]

http://eur-lex.europa.eu/legal (...) [HTML] [2000-12-31]

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Date index: 2023-06-14