Operator, Plasma Manufacturing, Narita Site / 成田工場 血漿分画製剤 製造担当者 製剤グループ（正社員）

Role summary

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This role supports plasma-derived medicine manufacturing at Takeda’s Narita Site. Responsibilities typically include operating and monitoring production equipment, following approved manufacturing procedures, recording batch and process data, performing cleaning and setup activities, and maintaining strict GMP, safety, and quality standards. Candidates are expected to have experience in manufacturing, pharmaceuticals, biotechnology, chemicals, food production, or a related technical environment. Attention to detail, reliable documentation, teamwork, and willingness to work shifts are important. Japanese communication skills are likely required for procedures and workplace coordination. Experience with GMP, aseptic or controlled manufacturing, equipment troubleshooting, and continuous improvement would be advantageous.

About the employer

Takeda Pharmaceutical Company is a major Japanese biopharmaceutical company headquartered in Tokyo, with operations in more than 80 countries and regions. Founded in 1781, Takeda develops and supplies medicines in areas including gastroenterology, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines. Its Narita Site in Chiba is an important manufacturing location, including production of plasma-derived products used to treat serious and chronic conditions. Takeda emphasizes patient-focused innovation, scientific quality, ethical conduct, workplace safety, and compliance with global Good Manufacturing Practice standards. Employees work in multinational teams and contribute to medicines that require highly controlled processes, accurate documentation, and strong collaboration across manufacturing, quality, engineering, and supply functions.