Saitama QA Staff (埼玉:QAスタッフ)

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Date: May 2, 2019

Location: Saitama, Saitama, JP








  1. Quality Assurance
  • Supply good-quality products seamlessly to Japan market.
  • Develop and maintain the up-to-date Quality System at Saitama site and assure that Quality System is fully aligned with the latest requirements by local HA, guidelines related to pharmaceutical industry and UCB Quality Policies/Standards.
  • Achieve the relevant KPI targets.
  1. Support and Training
  • Support associates to achieve site/team/personal goals.
  • Develop associate’s knowledge and skills.
  1. Continuous improvement
  • Engage in OE activities and enhance quality and/or productivity at Saitama site.
  1. HSE
  • Engage in HSE activities and assure own and associate’s health/safety.

Minimize the impact on environment.


-      More than 3 years’ experience working under GMP (QA, QC, Production or equivalent)

General knowledge about pharmaceutical drugs and production



  • Good knowledge/understanding of local GMP requirements
  • Good knowledge/understanding of guidelines like ICH, WHO and PIC/S GMP
  • Logical thinking
  • Fluent communication skill by local language

Basic communication skill by English (TOEIC: more than 730) is A+






















フレックスタイム制 (7:00-22:00) 7.5h×月間所定労働日数で清算

 昼休み 1時間

Job Segment: Pharmaceutical, Supply, QA, Quality Assurance, Science, Operations, Technology, Quality

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