QA Specialist
Location: NetherlandsSIRE 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.
Job Description
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.
Additional Information
- Last updated
- Employment type
- Full time
- Contract type
- Self employed
- Number of vacancies
- 1
- Min. experience
- Two years
- Min. education
- Bachelor
- Industry / category
- Jobs in Quality Control
