Our client is the largest manufacturer and distributor of medicines among the Netherlands. Their therapeutic areas include heart and vascular diseases, oncology, birth control, diabetes, reuma, fertility, vaccines, infectious diseases and hepatitis.
As a CSV Officer you will be responsible for the validation of the laboratory compuyter systems to ensure that quality procedures are in place.
- Reviewing and writing qualification documents (URS, protocols / reports...)
- Verification of qualification documents produced by external companies
- Creating Quality Assurance plans
- Writing Installation documents, Configuration Specifications and documentation index
- Determine with R&D Department which instrucments are needed
- Other tasks ad hoc
- 2+ years of experience in a similar role
- Experience with CSV of laboratory systems
- Background in pharma, medical devices, food or chemical industry
- Good communication skills in English
- Ability to work independently
For more information please contact email@example.com or +31 (0) 20 658 98 01.