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 companyOur client is a professional Clinical Research and Pharmaceutical organization, based in Waals-Brabant Belgium. Our client is an international company in clinical supplies and pharmaceuticals.
Role descriptionYou will be responsible for supporting the Qualified Person and act as the back-up QP. Most of all you are responsible for batch reviews and related activities. The duration of the project will be around 3 months with a good change on an extension.
Responsibilities- Review batch records
- Check GMP guidelines are being used the right way
- Execute product releases (clinical trials)
- Documentation and implementation in ERP systems
- Correct handling samples
- Act as back up QP
Requirements- Industrial Pharmacist or QP
- Languages: French (speaking and reading) English (reading and writing)