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Angel Luis Mayorga González

Angel Luis Mayorga González

Auxiliar de laboratorio

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location of Angel Luis Mayorga GonzálezGreater Valladolid Metropolitan Area

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  • Timeline

  • About me

    Analytical Development Manager en Curia

  • Education

    • European Compliance Academy

      2017 - 2017
      Stability by Design Pharmaceutical Forced degradation studies

      What is Stress Testing and what are Forced Degradations – regulatory view . Common degradation reactions of APIs and excipients. Forced degradation studies in the pharmaceutical industry. Photodegradation. Impurities and degradation products resulting from reactive APIs, excipients and their impurities. How to perform your own forced degradation study. How to ensure chromatographic detection of all degradation products. Mass balance in degraded samples of pharmaceuticals. Reactions and forced… Show more What is Stress Testing and what are Forced Degradations – regulatory view . Common degradation reactions of APIs and excipients. Forced degradation studies in the pharmaceutical industry. Photodegradation. Impurities and degradation products resulting from reactive APIs, excipients and their impurities. How to perform your own forced degradation study. How to ensure chromatographic detection of all degradation products. Mass balance in degraded samples of pharmaceuticals. Reactions and forced degradations in solid state. Comparative accelerated degradation rates. World Climatic zones for drug stability storage. Thermal Stress studies to support shipping/distribution. Excursions from storage label conditions. Show less

    • University of California San Diego on Coursera

      2017 - 2017
      Drug Development Pharmacy

      Regulatory Considerations When Filing an Investigational New Drug Application, Clinical Study & Start-up Activities, Clinical Trials: Phase 1, Clinical Trials: Phase 2, Industry Considerations with Phase III Clinical Trials, New Drug Application, Filing, Product Labeling

    • Doctor en Ciencias Quimicas

      1997 - 2001
      Doctor Quimica Analítica

      Licenciatura y doctorado por la Universidad de Valladolid

    • Universidad de Valladolid

      1990 - 1996
      Licenciado en Ciencias Químicas Analytical Chemistry

    • Universidad de Valladolid

      1996 - 1997
      Curso de aptitud pedagógica Química

  • Experience

    • GSK

      Jan 1997 - Jan 1999
      Auxiliar de laboratorio

      Quality Control Laboratory, analysis by chromatographic techniques of raw materials and finished products (batch release and stabilities) in GMP environment.

    • Gadea

      Jul 2000 - Oct 2003
      Technical Services Technician

      Process control, technical support to production, process optimization

    • Gadea Grupo Farmacéutico

      Nov 2003 - Nov 2007
      Quality Assurance Technician

      Batch release, internal-external audits, OOS, CAPA, change control

    • Gadea

      Dec 2007 - Dec 2010
      Quality Assurance Team Leader

      Customers and suppliers audits, internal audits, batch release, GMP training, CAPA, change control, OOS, SOP, APRs

    • Crystal Pharma

      Jan 2011 - Oct 2013
      Técnico Desarrollo Analítico y Validaciones

      Development of analytical methods, analytical validations, drafting specifications and test procedures.

    • Crystal Pharma S.A.U.

      Oct 2013 - Dec 2015
      Responsable de desarrollo analítico y validaciones

      Development of analytical methods, analytical validations, drafting specifications and test procedures.

    • Curia

      Jan 2016 - now
      Team Leader, Analytical Development, R&D API Division

      Development of analytical methods, analytical validations, compendial verification, drafting specifications and test procedures

  • Licenses & Certifications