GMP Spezialist (m/f/d)

GMP review of electronic production regulations (Master Batch Records) for batch documentation in biopharmaceutical production (upstream and downstream) using the BioMES 8 software Self-planning and control of electronic production regulations and electronic accompanying documents Maintenance of master data (material, object etc.) in BioMES 8 and SAP Administrative activities such as the creation and implementation of internal training measures, the collection of key figures, the incorporation of new colleagues, the processing of change control requests and audit preparation and supervision

Bachelor's degree in science, e.g. biotechnology, process engineering, chemical engineering or comparable, alternatively completed natural science vocational training, e.g. the pharmacist, chemist with several years of professional experience (optional training as a technician, industrial master) Experience in the pharmaceutical industry or other industrial manufacturing plants with good understanding of production processes Embossed IT affinity and pleasure in screen activities Experience in GMP environment Good knowledge of German and English in word and writing Communication and team skills An independent and precise operation and a high degree of self-initiative

Performance-oriented salary package according to qualifications and professional experience Attractive social benefits, for example holiday and Christmas money Holiday entitlement of up to 30 days a year Individual training with renowned partners Personal advice with individual career planning Monthly changing discounts, e.g. in large shipping houses, hotel chains, airlines, fashion houses and many more