Description
CSV Expert required!
We are looking or a Dutch speaking CSV expert to start ASAP
Are you interested in joining one of the largest companies in the Netherlands? Then please get in touch!
You will be doing:
- Implementation of computer system validation (CSV) for software such as process equipment (SCADA system), building services, analysis equipment within production and quality control, validation of Excel sheets
- Implementation of equipment qualification for production equipment and analyzers
- Adjustment of global regulations and transfer to local procedures. Working with global software tools (such as change management, training, deviations)
- Independent coordination of appointments and availability of equipment with other departments at the site, close cooperation with the IT department
- Responsible for the creation, revision and approval of GMP-relevant documents (qualification documents, SOPs) in Dutch/English
- Preparation of documents for official inspections and presentation in the audit (Dutch and English)
To be successful you will need to:
- You have completed a technical degree at the university/college or you have completed technical vocational training and professional experience in the qualification/validation area of the pharmaceutical industry
- Sound knowledge of qualification and CSV as well as GMP fair documentation
- Good knowledge of MS Office applications (Word, Excel, PowerPoint)
- Willingness to become familiar with various software applications.
- Dutch fluent in spoken and written and good English language skills
- They ensure regular work processes, plan systematically and organize their own area of responsibility efficiently
- You work effectively with others, share necessary information, share your knowledge, and contribute to achieving team goals through your work
- You work on essential tasks, finish what you start and you do not give up easily even when obstacles
Please get in touch with Gregory.