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Rie Pagh

Rie Pagh

Quality Manager

Followers of Rie Pagh625 followers
location of Rie PaghAars, North Denmark Region, Denmark

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  • Timeline

  • About me

    Q&E Manager hos V. Guldmann A/S

  • Education

    • Horsens Teknikum

      1992 - 1995
      Mechanical Engineer Welding Engineering Technology/Technician

  • Experience

    • Dansk Skalform A/S

      Nov 1995 - Dec 2007
      Quality Manager

      Dansk Skalform is a foundry that cast the small and large items both for automotive and other industries ISO 9001 implementation and certification. Department manager. Prepares documentation. Control of customer-specific requirements. Metallurgy and test methods Intermn audits Internal training

    • Scandinavian Brake Systems A/S

      Dec 2007 - Oct 2014
      Automotive Division Quality Manager

      Automotive Division Quality responsibleTS 16949 maintenance of certification.Department manager.Member of the factory manager groupSupplier AuditsInternal Audit / handling / trainingPrepares documentation, including FMEA, control plans, Instructions ect.LEAN projects.Internal TrainingControl of customer-specific requirements.November 2014 SBS sold to FTE

    • FTE automotive GmbH

      Nov 2014 - Feb 2015
      Quality Manager

      TS 16949 maintenance of certification.Department manager.Member of the factory manager groupQuality management SFMC SlovakiaSupplier AuditsInternal Audit / handling / trainingPrepares documentation, including FMEA, control plans, Instructions ect.LEAN projects.Internal TrainingControl of customer-specific requirements.November 2014 SBS sold to FTE

    • MAT Dania ApS

      Feb 2015 - Dec 2017
      Quality Manager

    • Guldmann

      Dec 2017 - now

      Quality ManagerISO 9001 maintenance of certification.ISO 13485 - Medical Devices compliance Regulatory requirements such as MDD, MDRQuality department manager QA and QCSupplier AuditsExternal audits from certification bureauInternal Audit / handling / trainingDevelop and implement process documentation.Internal Training Quality & Environmental ManagerISO14001 implementation, maintenance and certificationISO9001 maintenance and certification.ISO13485 - Medical Devices compliance MDR (Medical device regulation) implementation and maintenanceContinuous improvements of systems and processesInternal, external and supplier auditsRisk ManagementTraining

      • Quality Manager

        Dec 2017 - now

      • Q&E Manager

        Dec 2017 - now

  • Licenses & Certifications

    • CE Marking for Medical Device, EU Directive MDR

      MEDQURE
      May 2019

    • Lovpligtig arbejdsmiljøuddannelse

      Arbejdsmiljøcentret
      Mar 2011

    • Internal auditors according to ISO/TS 16949:2002

      Bureau Veritas Group
      Aug 2008

    • LEAN Behavior for Managers

      DI - Dansk Industri
      Aug 2012

    • ISO 14001 - Introduktion til og tolkning af DS/EN ISO 14001:2015

      FORCE Technology
      Sept 2020

    • ISO 9001: 2015

      DNV
      Sept 2017

    • Miljøledelse ISO 14001 – Diplomkursus

      Dansk Standard
      Nov 2019

    • Medical Device Quality Management System (QMS)

      Key2Compliance®
      Mar 2018

    • Auditorkursus vedr. Code of Conduct

      FORCE Technology
      Feb 2023

    • Klimaregnskaber i praksis – få nemt styr på jeres CO2-regnskaber

      Aros Business Academy
      Mar 2023