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Overview

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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Success

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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Opportunity

  • Innovation

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

  • Inclusive

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

  • Empowerment

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

  • Collaboration

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

  • Top Workplace

    Recognized for our culture and way of working, we’re one of only 13 companies to receive Top Global Employer® status for 2018.

  • Work-Life

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

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Quality Systems Head

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Job ID R0008078 Date posted 04/03/2019 Location Madrid, Spain

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Job Description

Major accountabilities

  • Implement, manage and control the documentation system (LEADs);
  • Implement, manage and control the system of deviations, CAPAs, change control, complaints and remaining modules (EQMS);
  • Implement, manage and control SAP system for quality related tasks;
  • Manage suppliers and service providers to assure they comply with local, international and corporate standards;
  • Execute the GMP training and work colloboratively with other departments to structure the the overall training process;
  • Review and approve protocols and reports of qualification / validation of equipment, processes, cleaning, including IT.
  • Whatever other task in compliance with the CBA (art.22 & art.26).
  • Carry out the internal control responsibilities set forth for the procedures of your job.

Skills, experiences and qualifications required for the job:

  • Experience working with systems (document management, ERP, excursion management, etc.);
  • Experience with document management;
  • Experience with change control management;
  • Experience with the management of suppliers;
  • Experience with GMP training;
  • Knowledge of qualification I validation, including IT
  • Leadership skills;
  • Experience working with complex organizations and the ability to work in all functions and with all levels of the organization where the owner may not have direct authority;
  • Bachelor of Natural Sciences, preferably in Pharmacy, Biology or Chemistry;
  • Minimum of 5 years of experience in the pharmaceutical industry;
  • Minimum of 3 years of experience in QA / QC

Locations

Madrid, Spain

Worker Type

Employee

Worker Sub-Type

Regular

Time Type

Full time

Job ID R0008078

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