NOORD BRABANT, Netherlands
They stand for innovative solutions for improving animal health. The company is based in Noord-Brabant.
You will be responsible for classification of laboratory systems as well as reviewing and writing qualification documents (URS, protocols/ reports, etc.).
- Responsible for classification of laboratory systems;
- Review and wite qualification documents;
- Close contact with internal customers;
- Verification of qualification documents produced by outside companies.
- Experience with computer system validation (CSV);
- Knowledge of System Development Lifecycle (SDLC) processes;
- Min. 3 years of experience within the Pharmaceutical industry;
- Experience with GxP, 21CFRpart11, GAMP;
- Fluent in EN.