Oscar De Miguel Hernández

Experience

• 

  Andromaco

  Oct 1993 - Jun 1994

  Tecnico responsable Seccion Materias Primas
• 

  Medinsa (Grupo Grunenthal España)

  Sept 1995 - Jun 2005

  • Tecnico Responsable Seccion Estabilidades

    Sept 2002 - Jun 2005

  • Tecnico Validaciones

    Mar 2001 - Sept 2002

  • Tecnico responsable seccion Control de Inspeccion y Proceso

    Sept 1995 - Mar 2001
• 

  Toll Pharma

  Jun 2005 - Apr 2018

  Manager of the Quality Area. I am responsible of the Quality System compliance of the company.I coordinate 2 departments:Quality Assurance Department (3 Thecnicians and 1 Administrative)In Process Control department (2 Thecnicians)

  • QUALITY MANAGER

    Jan 2012 - Apr 2018

  • QUALITY CONTROL & DEVELOPMENT MANAGER

    Sept 2010 - Jan 2012

  • CHEMICAL & MICROBIOLOGICAL LABORATORY MANAGER

    Jun 2005 - Aug 2010
• 

  SERVIER PLANTA DE TOLEDO

  Apr 2018 - Jul 2020

  QUALITY MANAGER

  Manager of the Quality Area. I am responsible of the Quality System compliance of the company.I coordinate 2 departments:Quality Assurance Department (3 Thecnicians)Quality Control Department (8 Thecnicians and 5 Analysts)

• 

  Biosearch Life

  Nov 2020 - Jan 2023

  GLOBAL QUALITY LABORATORIES MANAGER

  Global Manager of the Quality Laboratories. I am responsible for the global management of the Quality Control Laboratories of the company.I coordinate a team of 17 people, supervising all the company laboratories activities. (Labs sited in Caceres and Granada)

• 

  BIOSEARCH LIFE (KERRY GROUP)

  Jan 2023 - Jan 2024

  Site Quality Manager (Plan Extract Sites in Talayuela-Caceres & Peñafiel-Valladolid.

  Head of Quality, managing the Quality Assurance and Quality Control Departments. Hierarchical dependence of the Plant Leader and Functional dependence to Global Quality & Regulatory Director.

• 

  Kyowa Kirin International plc.

  Jan 2024 - now

  Senior Quality Assurance Specialist - Global Audit QA

  Senior Quality Assurance Specialist responsible of GXP Audits.Job Purpose:- Perform audits, including due diligence as requested by the business for the development and manufacture of products within the Kyowa Kirin Pharmaceuticals Group of companies.-To ensure that each product is developed, manufactured and supplied to the marketplace in compliance with cGxP requirements, Marketing Authorisations, company operating policies and procedures as well as business requirements.