Quality Manager
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 organisation, based in Oost-Vlaanderen Belgium.
-contact suppliers & subcontractors: documentation, batch record reviewing, deviations & process validation
-final product release
-stability studies
-customer complaint handling
-CAPA reports
-2 years experience in a similar role;
-2years experience in a pharmaceutical company;
-master’s degree (Pharma, Biotech, Life Sciences);
-speaking and writing fluently Dutch and English;
-organizational and analytical skills;
-mature & assertive;
-teamplayer and excellent communication skills;
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rutger Koning.
The Company
Our client (located near Gent) creates new ways to make life healthier in the field of consumer healthcare. Currently they have a interesting position for a QA specialist.Role Description
You will work within a quality team together with two other colleagues and you will report to the head of quality.Responsibilities
-transfer support of new products to Operations-contact suppliers & subcontractors: documentation, batch record reviewing, deviations & process validation
-final product release
-stability studies
-customer complaint handling
-CAPA reports
Requirements
-GMP and/or ISO 13485 knowledge;-2 years experience in a similar role;
-2years experience in a pharmaceutical company;
-master’s degree (Pharma, Biotech, Life Sciences);
-speaking and writing fluently Dutch and English;
-organizational and analytical skills;
-mature & assertive;
-teamplayer and excellent communication skills;
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Rutger Koning.
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