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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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  • 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.

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  • 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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Microbiology technician

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Job ID R0030563 Date posted 02/10/2021 Location Madrid, Spain

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Job Description

  • Perform quality control operations, including environmental monitoring activities, sterility test..
  • Complete daily manufacturing tasks following standard operating procedures and batch document instructions.
  • Ensure analytical and ancillary equipment and materials necessary are adequate, qualified and available as required for the different activities.
  • Follow gowning requirements and wear protective clothing over the head, face, hands, feet and body.
  • Collaborate in the material management activities (purchase, reception, approval, storage, control of expiry dates, etc)
  • Prepare quality documents by completing forms, reports, logs and records of equipment and batches.
  • Contribute to the preparation of reports to compile and summarise activities and results, including PQR, stability reports, BoAS and any other document issued by the department.
  • Whatever other task in compliance with the CBA (art.22 & art.26).


Madrid, Spain

Worker Type


Worker Sub-Type


Time Type

Full time

Job ID R0030563
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