QA System Specialist

vor 1 Tag

Aubonne, Schweiz Randstad Vollzeit

Jobdescription 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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