Recruiting Information

Quality Assurance Specialist

Background of recruitment:

With an increase in new and developing products including Roche/Genentech origin-products, the diversification of the supply chain, and increase in contract manufacturers, testing sites and suppliers, quality activities such as quality assurance, conclusion of quality agreement, CMO and supplier management and audits are increasing on an annual basis. For this reason, we are looking for flexible individuals who have a keen interest in GQP, QMS and GCTP/GMP/GDP to join our team.

Type of employment Regular employee
Description of work

  • Ensuring compliance to GQP/QMS, GMP/GDP/GCTP for manufacturing, control and distribution operations performed in the sites

  • Oversight of manufacturers of medical devices, regenerative medicine products, biopharmaceuticals and small molecules, and suppliers thoroughout product life cycle

  • Manage or support deviations, change control, and corrective and preventative action plans (CAPA) in manufacturing, testing sites and material suppliers

Required qualifications
  • Bachelor or master degree in science or engineering with experience of work in the pharmaceutical industry
  • Experience and background in manufacturing, materials management, QA/QC, auditing or preparation and conclusion of contracts is highly desirable
  • Good verbal communication and ability to keep excellent working relationships with peers and management
  • Good level of written and spoken English
Place of business Ukima Research Laboratories (Kita Ward, Tokyo)
Hours Flex time system (core time: 11:30–13:30)
Salary To be decided in accordance with our criteria
Application method

Please apply via the link below.

* We will not disclose applications to any third party.

* We will not use documents submitted by applicants for any purposes other than screening.


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