Patricia Fernández Fernández

Post-Harvest Manager at Linneo Health
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Contact Information
Location
Spain, ES
Languages
  • Español Native or bilingual proficiency
  • Inglés Full professional proficiency
  • Alemán Limited working proficiency
  • Francés Limited working proficiency

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Credentials

  • 2017 Barluenga Lectureship
    -
    Nov, 2017
    - Sep, 2024
  • Spanish Japanese Symposium on Modern Synthetic Methodology
    -
    Apr, 2017
    - Sep, 2024
  • 2016 Barluenga Lectureship
    -
    Nov, 2016
    - Sep, 2024
  • 11th Spanish-Italian Symposium on Organic Chemistry SISOC-XI
    -
    Jul, 2016
    - Sep, 2024
  • XXVI Reunión Bienal de Química Orgánica
    RSEQ
    Jun, 2016
    - Sep, 2024
  • Second Barluenga Lectureship
    -
    Oct, 2015
    - Sep, 2024
  • XXXV Reunión Bienal de la Real Sociedad Española de Química
    RSEQ
    Jul, 2015
    - Sep, 2024
  • Symposium on Selective Synthesis Mediated by Organometallic Compounds
    -
    Nov, 2014
    - Sep, 2024
  • Química: respuestas para un mundo mejor
    Fundacion Ramon Areces
    Oct, 2014
    - Sep, 2024
  • ICIQ-UNICAT Summer School
    ICIQ
    Jun, 2013
    - Sep, 2024
  • Nivel básico alemán - A2
    Escuela Oficial de Idiomas
    Jun, 2012
    - Sep, 2024

Experience

    • Spain
    • Pharmaceutical Manufacturing
    • 1 - 100 Employee
    • Post-Harvest Manager
      • Jan 2023 - Present

    • GMP Supervisor
      • Dec 2020 - Jan 2023

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Técnico de Calidad Junior
      • Jan 2019 - Dec 2020

      - Support to the manufacturing process of solid oral usage drugs and packaging product. - Review and approve both manufacturing and packaging orders. - Provide training to new incorporations in the team assuring compliance with Good Manufacturing Practices (GMP standards). - Management of technical documentation: manufacturing protocols, Standard Operational Procedures (SOPs), specifications of manufactured and packaging product, Work of Instructions, cleaning validation reports and other GMP documents. - Approve manufacturing equipment cleaning protocols and validation reports. - Provide weekly and monthly metrics of both production and packaging areas to assure compliance with Clase A metrics. - Review of Annual Product Review (APR) and specification changes according to regulatory requirements. - Daily support to the manufacturing process and management of incidents. - Support during regulatory inspections and audits. - Participation in packaging and manufacturing Quality Sessions. - Collaboration with other departments (Customer Service to manage urgencies, QC Laboratory, QA Incoming, engineering, etc.). Show less

    • Spain
    • Higher Education
    • 700 & Above Employee
    • PHD Student
      • Sep 2014 - Nov 2018

      Tesis doctoral en química orgánica: Cycloisomerization reactions with benzaldehyde derivatives: Synthesis of polycyclic systems containing isoquinoline and pyrrol frameworks. Tesis doctoral en química orgánica: Cycloisomerization reactions with benzaldehyde derivatives: Synthesis of polycyclic systems containing isoquinoline and pyrrol frameworks.

Education

  • CESIF
    Experto Profesional en Calidad Industrial y Procesos Farmacéuticos
    2021 - 2022
  • Euroinnova Business School
    Curso Práctico de Técnicas de Motivación y Liderazgo para el Trabajo en Equipo
    2021 - 2021
  • Universidad de Oviedo
    Doctor of Philosophy - PhD, Química orgánica
    2014 - 2018
  • University of Cambridge
    Certificate in Advanced English
    2017 -
  • Universidad de Oviedo
    Master of Science - MS, Química y desarrollo sostenible
    2013 - 2014
  • Universidad de Oviedo
    Licenciatura, Química
    2008 - 2013

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