募集要項
- 募集背景
- プロジェクトによる需要
- 仕事内容
-
Individual contributor project lead role- Primary responsibility is leading global internal audit project and ensuring implementation of quality plan at every stage of the Clinical Trial process/operations.
- Implement quality assurance regulations.
- Write and revise standard operating procedures.
- Support and facilitate audits and regulatory inspections.
- Support Quality Assurance Manager in supervision of all quality control aspects of the process (laboratories studies, clinical research, testing, operations).
- Ensure that standards are met and report potential issues either with quality or reliability of testing procedures.
- Lead implementation of new regulations.
- May support quality training.
- 応募資格
-
- 必須
-
- High school diploma or above
- Working experience in Medical Device Quality Assurance space
- Experience in internal and external audit
- 募集年齢(年齢制限理由)
- 下限なし ～ 65歳 （定年年齢を上限として募集するため）
- 雇用形態
- Contract
- 勤務地
- Chiba prefecture
- 年収・給与
- JPY7,000,000.00 - JPY9,000,000.00 per annum + competitive
- 選考プロセス
- 1-2 interview steps
