Beschreibung
Main tasks:- Ensuring the correct implementation of official requirements, as well as GMP and timely execution of the qualification of laboratory equipment
- Cooperation with device manufacturers within the framework of device qualifications
- Cooperation with various laboratories and support with troubleshooting
- Creation and review of qualification documents (e.g. User Requirement Specifications (URS), design, installation, functional and performance qualifications)
- Creation and review of SOPs and work instructions in the area of responsibility
- Processing of deviations (Quality Investigations), introduction of preventive and corrective measures (CAPA), as well as implementation of changes (Change Control) in the area of responsibilit
Qualifications:
- Successfully completed scientific or technological studies or comparable training with several years of professional experience, preferably with a focus on pharmaceutical, chemical, biotechnological or information technology (IT) areas
- Experience in the preparation and control of GMP documents
- Experience in CSV or qualification of production plants or analytical laboratory equipment
- Experience in the administration of analytical laboratory software is an advantage (e.g. Empower, Chromeleon, Softmax pro, tiamo, etc.)
- Very secure MS Office skills (Word, Excel, PowerPoint)
- Business fluent German and written English
Additional Notes: The position is located locally in Schaffhausen. It is possible to work from home a maximum of two days a week, but only if the project allows it
Sthree Switzerland is acting as an Employment Business in relation to this vacancy.