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The Senior Validation SME, Commissioning & Qualification Manager or Specialist at Takeda Pharmaceuticals in Japan is responsible for overseeing validation processes, commissioning, and qualification of engineering projects at the Hikari site. Candidates should have a strong background in engineering, validation, and project management, with experience in the pharmaceutical industry. They are expected to ensure compliance with regulatory standards and lead cross-functional teams to achieve project goals.
Takeda Pharmaceuticals is a global, values-based, R&D-driven biopharmaceutical leader headquartered in Japan. With a commitment to bringing Better Health and a Brighter Future to people worldwide, Takeda focuses on innovative medicines in oncology, gastroenterology, neuroscience, rare diseases, and plasma-derived therapies. The company operates in over 80 countries, emphasizing patient-centric values and a dedication to scientific innovation.
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