Associate QA Systems Mainz, Germany | full time | Job ID:8820 The Associate QA Systems supports the development of global document management within Veeva eQMS, aligning to One QMS initiatives. The role works cross-functionally supporting both training and document management. In close collaboration with BNT network, the candidate supports the harmonization and alignment of process improvement initiatives and helps the migration and operation of legacy documents to our new Veeva eQMS. Support global standards for Document Management within the GxP framework and the development of electronic Document Management Systems Support process improvements initiatives within our BioNTech network Manage document requests and support training requests in the various applicable electronic portals Perform applicable document control duties Work with stakeholders as needed to ensure a smooth transition from legacy systems to Veeva eQMS Experience in working with an electronic QMS (preferably Veeva) Profound knowledge of EU GMP and FDA regulations Work experience in manufacturing, quality control or quality assurance or other relevant area, ideally in a biotech or pharmaceutical company University degree in Chemistry, Pharmacy, Biology, Microbiology, Engineering or other technical/scientific area Carefulness and accuracy in the way of working, conscientiousness and detail-orientation Refined colloquial and correspondence and moderator skills in both German and English It's our priority to support you: Your flexibility: flexible hours | vacation account Your growth: Digital Learning | Performance & talent development | leadership development | Apprenticeships | LinkedIn Learning Your value: Your voice at the table | Culture on an equal footing | Opportunities to shape & impact | Support for your full potential Your health and lifestyle: Company bike Your mobility: Job ticket | Deutschlandticket Your life phases: Employer-funded pension | Childcare