Our client is the largest manufacturer and distributor of medicines within the Netherlands. Their therapeutic areas include heart and vascular diseases, oncology, birth control, diabetes, reuma, fertility, vaccines, infectious diseases and hepatitis.
As a Validation Engineer you will work with complex computerised laboratory systems in the QC Lab according to ALCOA Data Integrity rules.
- Classification of laboratory systems, whether computerized;
- Reviewing and writing qualification documents (URS, protocols / reports, etc.);
- Close contact with the internal customers;
- Verification of qualification documents produced by outside companies.
- Works with moderate work direction and is skilled and knowledgeable to the position.
- Experience in drafting CSV documents
- Laboratory background
- Software installation and configuration
For more information please contact Carla Garcia at email@example.com or +31 (0) 20 658 98 01.