Jacques Blümmel

Leitung F&E at Viscofan BioEngineering
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Contact Information
us****@****om
(386) 825-5501
Location
Weinheim, Baden-Württemberg, Germany, DE
Languages
  • Deutsch Native or bilingual proficiency
  • Französisch Native or bilingual proficiency
  • Englisch Full professional proficiency

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Credentials

  • Expert Technical Documentation Medical Devices
    TÜV Rheinland Group
    Jun, 2021
    - Oct, 2024
  • Der CE-Kennzeichnungsprozess für Medizinprodukte
    TÜV Rheinland Group
    Feb, 2021
    - Oct, 2024
  • Technische Dokumentation für Medizinprodukten
    TÜV Rheinland Group
    Feb, 2021
    - Oct, 2024
  • Design und Entwicklung von Medizinprodukten
    TÜV Rheinland Group
    Dec, 2020
    - Oct, 2024
  • Klinische Bewertung von Medizinprodukten
    TÜV Rheinland Group
    Dec, 2020
    - Oct, 2024
  • Risikomanagement nach ISO 14971:2019 / EN ISO 14971
    TÜV Rheinland Group
    Oct, 2020
    - Oct, 2024
  • Qualitätsbeauftragter
    TÜV Rheinland Group
    Oct, 2017
    - Oct, 2024

Experience

  • Viscofan BioEngineering
    • Germany
    • Biotechnology Research
    • 1 - 100 Employee
    • Leitung F&E
      • May 2023 - Present
  • invenio GmbH Engineering Services
    • Senior Expert Medical Devices Quality
      • Nov 2017 - Apr 2023

      * Temporary Employment at customer site [14.12.2017 – 30.09.2018]: ○ Design Control ○ Creation and maintenance of DHF relevant documents * since 10/2018: services for above mentioned customer under a service agreement in the field of development/technical documentation for medical devices * internal function as quality manager (ISO 13485) * Temporary Employment at customer site [14.12.2017 – 30.09.2018]: ○ Design Control ○ Creation and maintenance of DHF relevant documents * since 10/2018: services for above mentioned customer under a service agreement in the field of development/technical documentation for medical devices * internal function as quality manager (ISO 13485)

  • CeloNova BioSciences Germany GmbH
    • Group Leader R&D (07/2015 - end)
      • Jun 2007 - Mar 2017

      * Development of medical devices (class III) according to ISO 13485/ 21 CFR 820 * Project leading of research and development projects as well as the exploration of new application possibilities of already marketed products * Design control and risk management * Scientific external presentation (publications, presentations on congresses and symposia, marketing material, patents) * Training of colleagues, distribution partners and customers * Development of medical devices (class III) according to ISO 13485/ 21 CFR 820 * Project leading of research and development projects as well as the exploration of new application possibilities of already marketed products * Design control and risk management * Scientific external presentation (publications, presentations on congresses and symposia, marketing material, patents) * Training of colleagues, distribution partners and customers

  • Max Planck Institute for Medical Research
    • Germany
    • Research
    • 1 - 100 Employee
    • Group Leader (Post Doc)
      • 2005 - May 2007

Education

  • Ruprecht-Karls-Universität Heidelberg
    Dr. rer. nat., Chemie
    2001 - 2005
  • Ruprecht-Karls-Universität Heidelberg
    Diplom, Chemie
    1994 - 2001

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