Staff, Quality Assurance, Osaka Site / 大阪工場 製品保証グループ 製品保証担当

Role summary

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The role supports product quality assurance at Takeda’s Osaka manufacturing site. Typical responsibilities include reviewing manufacturing and testing records, handling deviations, change controls, CAPA, complaints, audits, and batch or product release activities in accordance with GMP and Japanese regulations. Candidates are expected to have experience in pharmaceutical quality assurance, manufacturing, quality control, or a related scientific discipline. Knowledge of GMP, quality systems, and regulatory requirements is important. Strong Japanese communication skills are likely essential, while English proficiency is useful for working with global Takeda teams. The successful candidate should be detail-oriented, analytical, ethical, and capable of making sound quality decisions while collaborating effectively with production, laboratory, engineering, and regulatory colleagues.

About the employer

Takeda Pharmaceutical Company is a Japan-headquartered global biopharmaceutical company with a history spanning more than two centuries. Its main focus areas include gastroenterology, rare diseases, plasma-derived therapies, oncology, neuroscience, and vaccines. Takeda operates research, manufacturing, and commercial facilities across Japan and international markets, serving patients in more than 80 countries. The company is known for its patient-focused approach, science-led innovation, and emphasis on ethical business practices. Its Osaka operations form part of Takeda’s important Japanese manufacturing and quality network. Employees typically work in highly regulated environments where product safety, data integrity, continuous improvement, and collaboration with global teams are central to daily responsibilities.