Quality Officer
Location: BelgiumSIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Pharmaceutical and Biotechnology organisation, based in Anvers Belgium.
- QA reviews voor batch release
- Document control, Change control
- Deviaties en non-conformances
- Assisteren in kwaliteitsplanning, meetings van management reviews organiseren
- CAPA's
- Ervaring met kwaliteitssystemen in medical devices
- Ervaring met kwaliteitsdocumenten reviewen
- Ervaring met deviaties, CAPA's, Non-conformances, auditing
- Vloeiend Nederlands en Engels
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
The Company
They are an international company that have a focus on different markets. The client provides equipement and services for laboratories.Role Description
U zal zich bezig houden met de ontwikkeling van QA. Onder uw verantwoordelijkheden vallen het onderhouden en verbeteren van het kwaliteitssysteem, volgens de ISO-13485 norm.Responsibilities
- Het organiseren en geven van trainingen- QA reviews voor batch release
- Document control, Change control
- Deviaties en non-conformances
- Assisteren in kwaliteitsplanning, meetings van management reviews organiseren
- CAPA's
Requirements
- Bachelor or Master in Life Sciences of u heeft een aantal jaren werkervaring opgedaan met de ISO13485 normering, in combinatie met een Bachelor of Master- Ervaring met kwaliteitssystemen in medical devices
- Ervaring met kwaliteitsdocumenten reviewen
- Ervaring met deviaties, CAPA's, Non-conformances, auditing
- Vloeiend Nederlands en Engels
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Amber Moet.
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