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Martin KadnerMK

Martin Kadner

Senior Project Manager | Manager Regulatory | CEO

€1,111/day
Hamburg, DE
15+ years

Average response time: 1 hour

Freelancer profile translated to English.
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About Martin

Through my many years of experience in research & development and since 2012 in management, I am aware of all processes within a company and can not only understand but also integrate all individual disciplines.
I look forward to helping you and your company move forward with my commitment!
  • German

    Native or bilingual

  • English

    Fluent

  • Spanish

    Basic

Can work on-site
Hamburg (up to 50km), Berlin (up to 100km), München (up to 100km), Frankfurt am Main (up to 100km), Leipzig (up to 100km), Hannover (up to 100km), Kiel (up to 100km), Köln (up to 100km), Stuttgart (up to 100km)

Experience

  • Kadner Consulting
    CEO
    DIGITAL AND IT
    February 2012 - Today (14 years and 6 months)
    Hamburg, Germany
    - Project/Program Management (agile and according to CMMI),
    - Quality Management ISO 9001 & ISO 13485
    including risk management according to
    ISO 14971, Configuration Management,
    - Technical Documentation (BSI: EAL, IT-Grundschutz),
    - Interim Management (CEO, CTO),
    - Auditor
    Management Medical Technology Program Management Project Management Semiconductor EU MDR
  • Philips GmbH Market DACH
    Customer Project Manager
    CONSULTING AND AUDITS
    June 2024 - July 2025 (1 year and 1 month)
    Hamburg, Germany
    Koordination und Entwicklung eines Auslieferungszentrums zur Vorkonfiguration von Patientenmonitoren und deren Modulen für den deutschen Markt.
    Entwicklung einer Cargobox für die Auslieferung der Produkte.
    Internationales Projektmanagement Facility Management CAD-Konstruktion
  • Philips Medizin Systeme Böblingen GmbH
    Transition/Acting Program Manager for EU MDR Transition in Production
    CONSULTING AND AUDITS
    February 2021 - April 2026 (5 years and 1 month)
    Böblingen, Germany
    - Coordination of activities for the transition of
    production of patient monitors from MDD to MDR
    - Preparation of business decisions based on
    regulatory, quality, and market data
    - Goals achieved so far: Transition of Class II
    products on time according to set audits or
    transition dates (Class I end of May 2021)
    - Medical Technology
    - Production
    Project Management Program Management Manager Regulatory Affairs

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Education

  • Manager Regulatory Affairs in Medical Technology
    University of Lübeck
    2014
  • Business Administrator (IWW)
    Fernuniversität Hagen
    2007

Certifications

  • IBM- Managing Successful Projects
    Philips EMEA Learning Services
    2005
  • DDI- Communicating for Results
    Philips EMEA Learning Services
    2005

Skill set

Categories