Hays – Working for your tomorrow | Germany | Mannheim | Full time | Published since: 19.03.2025 on stepstone.de
MES Change Specialist (m/w/d)
With over 15 years of experience in the classic pharmaceutical industry, biotechnology, chemistry and medical technology, we know the key contact persons who write out demanding tasks with potential. The high demand for personnel opens up exciting opportunities for dedicated professionals and managers to develop professionally and work on their own careers. As a specialized staff consultancy with an international network, we offer you decisive advantages - and this is completely free of charge for you. Register and benefit from interesting and matching positions and projects. JOBV1_EN
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With over 15 years of experience in the classic pharmaceutical industry, biotechnology, chemistry and medical technology, we know the key contact persons who write out demanding tasks with potential. The high demand for personnel opens up exciting opportunities for dedicated professionals and managers to develop professionally and work on their own careers. As a specialized staff consultancy with an international network, we offer you decisive advantages - and this is completely free of charge for you. Register and benefit from interesting and matching positions and projects. Central respondent for change requests from the value streams A, B and C, e.g. of the electronic master batch record in the MES Collection of change requests, cross-value flow harmonisation of requirements for the MES MBR Support of the operational areas during or through the creation, planning and coordination of the necessary changes (Planned Event Owner) Communication of changes with the running support organization, testing the MBR requirement specification Implementation of risk analyses based on the requirement specification Create test plans for the MBR recipe verification Coordination and implementation of verification of MBR recipes by screening tests and documented verification tests
Completed scientific training e.g.Pharmacant or comparable qualification Professional experience in the GMP environment, additional qualification as technician/master or Bachelor in the scientific field desirable Found professional experience in the GMP environment First professional experience in the application of IT applications in the GxP-regulated environment of pharmaceutical production First knowledge in the pharmaceutical production processes Very good knowledge of German in word and writing Very good standard office software knowledge Good English knowledge of word and writing Good general GxP knowledge and especially for the Computerized System Validation (CSV) Passion for System Knowledge (PharmaSuite)
Varied activity in a renowned company Demanding and varied tasks in a future-oriented and innovative industry Annual holiday entitlement of 30 days Care in the entire application process Support in the ongoing project by our team JOBV1_EN
Company location
Location
![]() | Hays – Working for your tomorrow | |
Mannheim | ||
Germany |
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