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  Erfahrung/Know-how in: DICOM, Clinical Workflow Know-How, Risikomanagement und Risikoanalyse für Medizinprodukte, Medizinprodukterecht, Klinische Bewertung von Medizinprodukten, Software Engineering, Project Management, Product Marketing, Product Management, Quality Management, Lieferanten-Qualitätsmanagement, Test Management, Complaint Handling for Medical Devices, Medical Engineering Solutions, Mobile Communication, Telecommunication, Semiconductors, Medizintechnik, Mobilkommunikation, Telekommunikation, Halbleiter, QM, QA, SQM, Process Management, Integrierte Managementsysteme, Software Quality Assurance, Software Configuration Management, Software Risk Management, Software Estimation, TQM, ISO9000:2000, ISO TS 16949, ISO15504 (SPICE), DIN EN ISO 19011, BS OHSAS 18001, DIN EN ISO 14001, ISO13485:2003 + AC 2007, ISO 14971, IEC 80001, DIN EN 62304, FDA QSR 21 CFR 820, FDA Regulatory Requirements, JPAL- Regulatory Requirements, CMDCAS- Regulatory Requirements, Regulatory Requirements China, Regulatory Requirements Rußland, TL9000, Capability Maturity Model (CMM), Capability Maturity Model Integration (CMMI), PSP (Personal Software Process), TSP (Team Software Process), agiler Entwicklungsprozess, Lean Management, FMEA, 8D, KVP, PDCA Cycle, Six Sigma (Grundlagen), Multi Cultural Effectiveness, Transaktionsanalyse, Management by Objectives, Konfliktmanagement, BWL für Führungskräfte & Ingenieure, disziplinarische Personalführung

• Interests

  Squash, Volleyball, USA, Italien

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  Employee

Educational background

• Languages

  German, English