Judit Navarro Parra

QA Specialist at Anaconda BioMed
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Contact Information
us****@****om
(386) 825-5501
Location
Greater Barcelona Metropolitan Area, ES
Languages
  • Spanish Native or bilingual proficiency
  • Catalan Native or bilingual proficiency
  • English Full professional proficiency
Skills

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Credentials

  • Certificate in Advanced English
    Cambridge English Language Assessment
    Aug, 2016
    - Nov, 2024
  • First Certificate in English
    Cambridge English Language Assessment
    May, 2014
    - Nov, 2024
  • YLE Flyers
    University of Cambridge
    Jun, 2010
    - Nov, 2024

Experience

  • Anaconda BioMed
    • Spain
    • Medical Equipment Manufacturing
    • 1 - 100 Employee
    • QA Specialist
      • Nov 2022 - Present

      Management of Quality Control activities. Development, modification and adaptation of SOPs to the QMS. BEAS software configuration and management. Equipment management: Elaboration and review of plans and protocols, coordination, scheduling, execution, review and supervision of calibration, maintenance and qualification activites of equipment and facilities. Processes and test methods: elaboration/review of plans and protocols, planning, coordination, execution/review and supervision of processes and test methods. Collaboration in internal and external audits and inspections by Health Authorities and Notifying Bodies. Training of personnel in Quality issues and assurance of their application and compliance. Show less

  • B. Braun Group
    • Germany
    • Medical Equipment Manufacturing
    • 700 & Above Employee
    • Quality Control Laboratory Technician
      • Sep 2017 - Nov 2022

      To be part of the HPLC chromatographic analytical methods (OpenLab) and kinetic methods of endotoxin detection (Pyros EQS) validations in accordance with current GMPs and Pharmacopoeia regulations: Drafting and designing the validation protocols, worst case matrices and final reports. Studying and deciding the parameters and acceptance criteria and carrying out the tests as first analyst.To be part of the assays carried out in the QC Laboratories, from the sample reception, test performance to product release by SAP.Internal System Audits.SOPs drafting and modification.Management and investigation of incidents and developement of reports and OoS.Management of purchase requests and receipt of materials and reagents.Development and application of improvement measures at an operational and preventive level under the Shopfloor Management (SFM) philosophy. Show less

    • Trainee analyst in Chemical Quality Control Laboratory
      • Feb 2019 - May 2019

      HPLC chromatographic analytical methods (OpenLab) validation in accordance with current GMPs and Pharmacopoeia regulations: Drafting and designing the validation protocols, worst case matrices and final reports. Studying and deciding the parameters and acceptance criteria. Carrying out the test as the first analyst.

    • Trainee analyst in Biological Quality Control Laboratory
      • Jul 2017 - Sep 2017

      Environmental monitorization, endotoxin detection assay and intermediate product assay.

Education

  • Bureau Veritas
    Internal Auditor at QMS, EMS and OH&S MS
    2019 - 2020
  • Universitat Autònoma de Barcelona
    Master in Pharmacology, Preclinical pharmacology research methods specialisation
    2018 - 2019
  • Universitat Autònoma de Barcelona
    Degree in Microbiology
    2014 - 2018

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