Operator, Plasma Manufacturing, Narita Site / 成田工場 血漿分画製剤 製造担当者（契約社員）

Role summary

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Takeda is seeking a contract manufacturing operator for its Narita plasma fractionation facility. The role typically involves operating and monitoring production equipment, handling plasma-derived pharmaceutical products, preparing materials, recording manufacturing data, and following approved procedures. Candidates are expected to work carefully in a GMP-regulated environment, maintain high standards of hygiene and safety, and support investigations or continuous-improvement activities. Experience in pharmaceutical, chemical, food, or other regulated manufacturing is advantageous. A science or technical background, basic documentation and computer skills, willingness to work shifts, and the ability to communicate effectively in Japanese are likely requirements. Reliability, attention to detail, teamwork, and strict compliance with quality procedures are essential.

About the employer

Takeda Pharmaceutical Company Limited is a global, research-driven biopharmaceutical company headquartered in Japan. Founded in 1781, it develops and supplies medicines in areas including gastroenterology, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines. Takeda operates research, manufacturing, and commercial organizations across numerous countries and employs a diverse international workforce. Its manufacturing network produces complex medicines under strict Good Manufacturing Practice, quality, safety, and regulatory standards. The Narita site in Chiba is associated with the production of plasma-derived pharmaceutical products, which require carefully controlled processes because they originate from donated human plasma. Takeda emphasizes patient focus, integrity, inclusion, collaboration, and continuous improvement. Employees in manufacturing roles contribute directly to reliable supply, product quality, and patient safety.