メディカル・バイオ - メディカルGQP・GMP・品質保証・品質管理

Major Accountabilities/Responsibilities

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.
- Make decision for batch release.

2. Support and Training
- Support associates to achieve site/team/personal goals.
- Develop associate’s knowledge and skills.

3. Continuous improvement
- Lead to implement new / latest GMP requirement, regulations and computerized system for all Saitama site.
- Engage in OE activities and enhance quality and/or productivity at Saitama site.

4. HSE
- Engage in HSE activities and assure own and associate’s health/safety.
- Minimize the impact on environment.

■休日：週休二日制, 土, 日, 祝日, 夏季休暇, 年末年始

More than 5 years’ experience working under GMP (QA, QC, Production or equivalent), General knowledge about pharmaceutical drugs and production

■職種未経験者：不可