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SIRE Life Sciences®

QA Specialist

Netherlands, zagranica Pełny etat

SIRE Life Sciences®

QA Specialist

Location: Netherlands

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Medical Devices organization, based in Noord-Holland Netherlands.

OTC bedrijf die consumenten welzijn producten maakt. Deze producten zijn gebonden aan Medical Devices richtlijnen.

ROLE DESCRIPTION

- QMS requirements bijhouden (ISO13485, ISO9001, 93/42 EEC)
- Management representative en verantwoordelijk voor audits
- Complaint handling
- CAPA
- Suppliers
- Notified bodies
- ETC


RESPONSIBILITIES

Lange vacaturetekst op aanvraag verkrijgbaar.

REQUIREMENTS

- Ruime kennis van ISO13485
- Zelfstandigheid
- Wonend in of nabij Amsterdam, bedrijf alleen bereikbaar met OV
- Liefst enige chemische/farmaceutische kennis

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.

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SIRE Life Sciences®

Opis stanowiska

SIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!

THE COMPANY

Our client is a professional Medical Devices organization, based in Noord-Holland Netherlands.

OTC bedrijf die consumenten welzijn producten maakt. Deze producten zijn gebonden aan Medical Devices richtlijnen.

ROLE DESCRIPTION

- QMS requirements bijhouden (ISO13485, ISO9001, 93/42 EEC)
- Management representative en verantwoordelijk voor audits
- Complaint handling
- CAPA
- Suppliers
- Notified bodies
- ETC


RESPONSIBILITIES

Lange vacaturetekst op aanvraag verkrijgbaar.

REQUIREMENTS

- Ruime kennis van ISO13485
- Zelfstandigheid
- Wonend in of nabij Amsterdam, bedrijf alleen bereikbaar met OV
- Liefst enige chemische/farmaceutische kennis

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Tim Thuijs.

Dodatkowe informacje

Ostatnia aktualizacja
Wymiar etatu
Pełny etat
Rodzaj umowy
Własna działalność
Liczba wakatów
1
Min. doświadczenie
2 lata
Min. wykształcenie
Wyższe licencjackie
Branża / kategoria
Praca Kontrola jakości