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Validation Specialist

Ospedaletto, Italy, Pisa, Italy


Every day, employees working in Takeda’s Global Manufacturing and Supply Chain, and Global Quality business unit are shaping the future of healthcare. They are breaking down barriers and ensuring our life-changing medicines are available, accessible, and affordable to patients. Life-changing for you. Life-changing for patients.

Global Manufacturing and Supply Chain, and Global Quality is the backbone of Takeda, and our employees are the guardians for our patients, our products, and our reputation. As a member of our team, we can offer you the opportunity to grow in a meaningful career, develop your skills, and come to work every day knowing that what you do makes a genuine difference.

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What makes a successful member of our team? Check out the traits we’re looking for and see if you have the right mix.

  • Agile
  • Ambitious
  • Analytical
  • Collaborative
  • Enthusiastic
  • Entrepreneurial

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  • Bold initiatives, continuous improvement, and creativity are at the heart of how we bring scientific breakthroughs from the lab to patients.

  • Here, you will feel welcomed, respected, and valued as a vital contributor our global team.

  • Through trust and respect, you will have genuine support from leaders, managers, and colleagues to do your best work.

  • A strong, borderless team, we strive together towards our priorities and inspiring mission.

  • Recognized for our culture and way of working, we’re one of only 13 companies to receive Top Global Employer® status for 2021.

  • Our people-first mission extends beyond patients to include their families, communities, and our own Takeda family.

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Validation Specialist

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Job ID R0033465 Date posted 04/20/2021 Location Ospedaletto, Italy; Pisa, Italy

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Job Description

  • Partecipa ai meeting per la definizione delle strategie di convalida delle apparecchiature/ambienti/utilities e dei sistemi computerizzati del sito.
  • Scrive e revisiona i protocolli e report di convalida delle apparecchiature/ambienti /utilities e dei sistemi computerizzati del sito.
  • Scrive e revisiona documenti di analisi del rischio e di validation plan delle apparecchiature/ambienti /utilities e dei sistemi computerizzati del sito.
  • Scrive e revisiona procedure di reparto
  • Esegue attività di training relative alla validazione.
  • Partecipa all’esecuzione o occuparsi della supervisione dell’esecuzione dei protocolli di convalida per quanto di competenza.
  • Si interfaccia con ditte esterne o con altre funzioni dello stabilimento per il coordinamento delle attività di convalida/CSV.

Attitudini e competenze:

  • critical thinking
  • capacità di coordinamento e gestione di personale esterno
  • capacità di comunicazione e attitudine al team working
  • doti organizzative ed analitiche
  • orientamento al risultato e al problem solving
  • buona conoscenza della lingua inglese scritta e parlata
  • ottima conoscenza dei principali pacchetti informatici
  • consolidata esperienza di validazione di sistemi computerizzati in ambito farmaceutico

Titolo di studio:

Laurea Informatica, Ingegneria Elettronica o titoli equivalenti


ITA - Pisa

Worker Type


Worker Sub-Type


Time Type

Full time

Job ID R0033465
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