SIRE® 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 Oost-Vlaanderen Belgium.

The Company

Onze klant is een farmaceutisch bedrijf in de regio Oost-Vlaanderen.

Role Description

In deze rol bent u verantwoordelijk voor kwaliteit in een GMP gereguleerde omgeving.

Responsibilities

- Goedkeuring van Validatie Documenten
- Review van kwaliteitsdocumentatie (URS review, change control)
- Geven van trainingen en ontwikkelen van trainingsmateriaal
- CAPA Management en implementatie
- Samenwerking met QP in de vrijgave van producten
- Zorgdragen voor kwaliteit in GMP omgeving

Requirements

- 3 tot 5 jaar werkervaring
- Ervaring in GMP omgeving
- 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 Daniel Woudenberg.