Dr. Julika Pristup

Angestellt, Requirements Engineer, Miltenyi Biotec B.V. & Co. KG

Leverkusen, Deutschland

Über mich

Work: Molecular Diagnostics – Development and improvement of medical devices and workflows according to national and international directives, (ISO 13485, 21 CFR Part 820.30). Working in international cross-functional teams with focus on system integration, matching the needs of underlying applications (infectious diseases, NGS – oncology), platform and software. Characteristics: Conscientious, accurate, reliable Strengths: Eye for detail, empathy, solution-oriented thinking Motivation: Better quality of human life, maximum customer satisfaction, ensure high standards

Fähigkeiten und Kenntnisse

Molecular Diagnostics
DHF Dokumentation
Produkt Entwicklung
Design Control
Verifikations-Tätigkeiten
Schnelle Auffassungsgabe
Präsentationsfähigkeit
Anpassungsfähigkeit
Zielstrebigkeit
Zuverlässigkeit
Kontaktfreudigkeit
Selbstständigkeit
Qualitätsmanagement

Werdegang

Berufserfahrung von Julika Pristup

  • Bis heute 1 Jahr, seit Juli 2023

    Requirements Engineer

    Miltenyi Biotec B.V. & Co. KG
  • 3 Monate, Apr. 2023 - Juni 2023

    Senior Usability Engineer

    QIAGEN GmbH
  • 1 Jahr, Apr. 2022 - März 2023

    Usability Engineer

    QIAGEN GmbH
  • 6 Jahre und 3 Monate, Jan. 2016 - März 2022

    Scientist R&D

    QIAGEN GmbH

    *Clonal Amplification and Sequencing: design of experiments, laboratory work, documentation and sequencing data analysis. Best Practice Lead in international Verification- and System Integration-Campaigns – coordination and guidance of laboratory technicians, creation of experimental schedule, documentation, coordination of interdisciplinary problem solutions. *Workflow subsystem alignment *Life cycle management.

  • 1 Jahr und 2 Monate, Nov. 2014 - Dez. 2015

    Scientist R&D - QIAsymphony RGQ platform

    QIAGEN GmbH

    *Design of experiments and verification activities (with regard to liquid-handling and scripting) including coordination and guidance of the laboratory team. *IVD application development: platform-related documentation according to Design Conrol directives (21 CFR 820.30, ISO 13485) at the interface between software and application, review of DHF-relevant documents. *Preparation and guidance of project-associated workshops for team members

Ausbildung von Julika Pristup

  • 3 Jahre und 9 Monate, Mai 2010 - Jan. 2014

    Chemie

    Universität zu Köln

    Biochemie

Sprachen

  • Deutsch

    Muttersprache

  • Englisch

    Fließend

  • Französisch

    Grundlagen

Interessen

CrossFit
Klavierspielen
Reisen

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