Description
CSV/EQ Specialist Wanted in Belgium for major client
We are looking for:
- 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 analysers
- 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.
- Responsible for the creation, revision and approval of GMP-relevant documents (qualification documents, SOPs) in English
- Preparation of documents for official inspections and presentation in the audit.
Qualifications
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)
Recruiting now - get in touch if interested.