Mireia Castillón Melero

Head of Lean Agile Centre of Excellence at European Medicines Agency
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Contact Information
us****@****om
(386) 825-5501
Location
Netherlands, NL
Languages
  • Español Native or bilingual proficiency
  • Catalán Native or bilingual proficiency
  • Inglés Full professional proficiency
  • Francés Native or bilingual proficiency

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5.0

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Paolo Tomasi

Mireia is efficient and professional in completing her tasks, and a pleasure to work with.

Josele Sanchez Juan

Mireia apunta maneras!!!. Además de poseer una extraordinaria formación científica "tiene angel", quiere "saberlo todo", es inconformista y posee un espíritu de superación que acaba por envolver a quienes pretenden formarle. Es la alumna que, entre un montón de estudiantes que cada año pasan por tus manos... siempre recuerdas. Desconozco si finalmente optará por dedicarse a la parte técnica de la industria farmacéutica; si así fuere, el Marketing de "este negociado", tan necesitado de sabia nueva, de gente capaz de romper con todo lo que hasta ahora hemos hecho y "parir" nuevos conceptos, nuevos sistemas, nueva FILOSOFÍA habrá perdido un diamante en bruto". Mireia sólo necesita estar al lado de alguno de LOS GRANDES para aprenderlo todo y superarlos, y SUPERARNOS....

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Experience

    • Netherlands
    • Government Administration
    • 700 & Above Employee
    • Head of Lean Agile Centre of Excellence
      • Feb 2023 - Present

      Lead the Agile Transformation (SAFe) at EMA and support the Agile Way of working within the Organisation and the Network

    • Digitalisation Transformation Programme Manager
      • Sep 2017 - Jan 2023

      Implemented several SF modules (SAP) in HR domain: recruitment, onboarding, Performance and Development and LMS.

    • HR Business Partner and HR Change Manager
      • Mar 2018 - Feb 2020

      Supporting the Agency’s transformation to overcome the new upcoming challenges

    • Patient Registries Project Manager
      • Jan 2017 - Dec 2017

    • EU Network Training Project Manager
      • Apr 2014 - Dec 2016

      - Project manager of Learning Mangement System implementation for the EMA staff and National Competence Authorities (European Regulatory Network)- Management of EU Network Training Centre secretariat and services- Implementation of Competency framework and scientific, regulatory and Telematics curricula for the European Regulatory Network.

    • IT Liaison Officer
      • May 2013 - Apr 2014

      My role as IT Liaison Officer has enabled EMA to better understand and analise the IT stakeholders (mainly NCAs and Industry) in the framework of the new EU Telematics Governance. My main tasks were as follows: Manage the complete ICT stakeholders landscape for both internally and externally, Support the Head of ICT Unit in his strategic governance and communication challenges towards the ICT stakeholders and represent the agency in ICT related matters as required, Assist the Head of ICT Unit to lead, develop and manage – both inside and outside of EMA – the ICT Telematics governance and overlook all ICT Telematics programmes, Follow up on International Standardisation supporting colleagues involved in this process. Show less

    • Head of Unit support in the Veterinary Medicines and Product Data Management Unit
      • Nov 2011 - Apr 2013

      Playing a key role in the business activities conducted within the Head of Unit Support Team of the Veterinary Medicines and Product Data Management Unit in the fields of planning and reporting, stakeholder relations and range of long and short term projects (such as internal reorganisation exercise during November 2012 and March 2013), particularly those with cross agency or externally facing interactions.

    • Netherlands
    • Government Administration
    • 700 & Above Employee
    • Trainee at the Pharmacovigilance and Risk Management Sector (EMA traineeship Program)
      • Oct 2010 - Jun 2011

      Pharmacovigilance and Risk Management Sector (Communication & Networking Section) Institution: European Medicines Agency (EMA), London Main activities: 1. PROTECT (IMI) project: Study of stratification methods for the Eudravigilance Database. 2. Risk Communication: Conduct of a literature-based study on Risk Communication for vaccines, using the example of pandemic influenza and HPV vaccines. 3. Pharmacovigilance Working Party (PhVWP): Conduct of an analytic PhVWP Annual Report covering 2009 and 2010. Presentation of the results of this Report to the Member states in February 2011. Show less

    • France
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Intern, Technical Direction & Quality Assurance Department
      • Sep 2009 - Sep 2010

      Main activities: 1. Quality Assurance activities: •Responsible for Product Technical Complaint Management. •Management of Quality of Documents. •Writing SOPs for Product Technical Complaints. 2. Technical Direction activities: •Development of a document management tool in conjunction with the IT department. •Support the conduct of external audits to manufacturing companies in business partnership with Sanofi-Aventis. •Support the development of the new online personal training tool including the communication to the staff. Show less

    • Intern in the Pharmacy Service at Taipei Medical University Hospital. Taipei, Taiwan
      • Jul 2009 - Aug 2009

      Main activities: 1. Participation in a clinical pharmacy project in the paediatric unit. 2. Support in the research and development in the oncology laboratory. Main activities: 1. Participation in a clinical pharmacy project in the paediatric unit. 2. Support in the research and development in the oncology laboratory.

    • Belgium
    • Hospitals and Health Care
    • 500 - 600 Employee
    • Intern, Pharmacy Service
      • Sep 2008 - Jul 2009

      Main activities: Learning the basics of a Belgian hospital and competences of a Pharmacist in Belgium and development of the following studies: 1. “The Pain treatment of children: First observation of Tramadol usage” (published in the Pharm World Sci (2010) 32:212–309) 2. “The freezing of Vancomycin eye drops”. The main goal of these studies was to increase the patients’ clinical assistance and to reduce the hospital costs. Main activities: Learning the basics of a Belgian hospital and competences of a Pharmacist in Belgium and development of the following studies: 1. “The Pain treatment of children: First observation of Tramadol usage” (published in the Pharm World Sci (2010) 32:212–309) 2. “The freezing of Vancomycin eye drops”. The main goal of these studies was to increase the patients’ clinical assistance and to reduce the hospital costs.

    • United Kingdom
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Intern, Quality and Production Departments. Cairo, Egypt.
      • Jul 2008 - Aug 2008

      Main activities: 1. Support in the Compliance department on Production and Quality Assurance procedures. 2 Contribution to the development of new methods in the Analytic Control laboratory. Main activities: 1. Support in the Compliance department on Production and Quality Assurance procedures. 2 Contribution to the development of new methods in the Analytic Control laboratory.

    • Wellness and Fitness Services
    • 200 - 300 Employee
    • Intern, Pharmacy Service
      • Jul 2007 - Aug 2007

      Main activities: 1. Control and management of the expiry date of medicines used in the Emergency and Intensive Care Unit (UCI). 2. Extemporaneous preparation of unit dose medications. Main activities: 1. Control and management of the expiry date of medicines used in the Emergency and Intensive Care Unit (UCI). 2. Extemporaneous preparation of unit dose medications.

    • Spain
    • Food and Beverage Services
    • 700 & Above Employee
    • Trainee, Quality laboratory
      • Jul 2006 - Aug 2006

      1. Responsible for the development and adjustment of gas chromatographs. 2. Practical operation of the quality control laboratory. 1. Responsible for the development and adjustment of gas chromatographs. 2. Practical operation of the quality control laboratory.

Education

  • Gladwell Academy
    Certified SAFe 5 Program Consultant, Lean-Agile
    2023 - 2023
  • CIPD
    Diploma in Human Resource Management (QCF), Human Resources
    2016 - 2017
  • Universitat de Barcelona
    Master in Business Administration for Pharmaceutical Industries, Main subjects: Pharmaceutical Marketing, Regulatory Affairs, Patents, Quality Control, GCP, GMP, ISO
    2009 - 2011
  • Universitat de Barcelona
    Master's degree, Pharmacy
    2006 - 2009
  • Universitat Autònoma de Barcelona
    Master’s degree, Chemistry
    2002 - 2006

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