Mestre Justine

Mestre Justine

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location of Mestre JustineBordeaux et périphérie

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  • Timeline

  • About me

    Associate Manager Spine QA NPI

  • Education

    • Compliance guru

      2020 - 2020
      Certificate IRCA ISO 13485:2016
    • IUT Montpellier

      2000 - 2002
      GEII
    • International Institute Of Management

      2019 - 2019
      Certificate EDUCATION
    • Polytech'Montpellier

      2003 - 2005
      Engineer's degree Microelectronics and Automatics
  • Experience

    • Valeo CDA

      Dec 2005 - Mar 2016

      Valeo is a manufacturer specialized on conception, production of embedded systems and module for automotive industry.Valeo is present all around the world in order to be closer to its customers.The Valeo mindset is based on 5 axis to ensure the customer satisfaction (Product development, Involvement of personnel, Supplier intergation, Production sustem and Total quality).As project quality engineer, I have the following responsabilities:- Manage the quality in project : Monitor the quality roadmap and follow of the customer milestones.Detect, prevent and react when a risk is identified.- Respect the build in quality standards for the critical characteristics and challenge other project team members on their activities- Ensure the use of the design tools and change tools (DFMEA, PFMEA, DRBFM, DV&PV, 4M), check the other project feedbacks are taken into account (Lesson Learned Card)- Support the supplier management activities- Get validated Initial Samples from the customer:Define the control plan, participate to the FDPR (Full Day Production Run) and prepare initial samples - Ensure the QRQC (Quick Response Quality Control) rules are applied. Show less

      • Quality Engineer

        Sept 2013 - Mar 2016
      • Hardawre Design Leader

        Sept 2008 - Aug 2013
      • Hardware Designer

        Dec 2005 - Aug 2008
    • Stryker

      May 2016 - now

      - Lead auditor IRCA ISO 13485:2016- Process risk management (PFMEA) and inspection plan follow-up- Ensure the quality level of manufacturing process documentations- Sub-contractor manufacturing qualification follow-up (PPAP)- Approval & release of FAI (First Article Inspection) products- Non-Conformity management ; Define and apply corrective and preventive actions (FTA, 4D)- Write project quality report at launch, calculate project KPI- Sustain and improve procedures for the industrialization of new products- Introduction of Stryker harmonized tools to the Cestas (France) and La Chaux de Fonds (Switzerland) manufacturing sites; Training and procedure update. Show less

      • Associate Manager Spine QA NPI

        Feb 2024 - now
      • Senior Staff Quality Engineer

        Sept 2022 - Feb 2024
      • Staff Quality Engineer

        Aug 2018 - Sept 2022
      • Senior Advanced Quality Engineer

        Jan 2017 - Jul 2018
      • Advanced Quality Engineer

        May 2016 - Dec 2016
  • Licenses & Certifications