QA System Specialist
Vor 2 Tagen
As member of the Quality System & Compliance group, you will be responsible for the daily operational activities relating to training, documentation and archiving processes:
Documentation and archiving:
- Manage the distribution and life cycle of GxP documentation.
- Administration of operational activities.
- Administrate active BCP once it's activated.
- Act as key user for the documentation management system (DMS)
Training:
- Administration of operational activities
- Provide trainings for areas under your responsibility
- Act as key user for Learning Management System LMS
Projects:
- Process improvement of areas under your responsibilities
- Automatization of routine tasks (with tools like Power Apps, Power Automate)
Qualifikationen
- Bachelor in scientific education.
- 2 years in pharmaceutical industry.
- Experience in training, documentation management and archiving process.
- Experience in Quality Assurance.
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