募集要項
- 募集背景
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<About the Role>
1 Individual contributor that works under limited supervision.
2 Applies subject matter knowledge.
- 仕事内容
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<About the Role><Main Responsibilities>
1.Individual contributor that works under limited supervision.
2.Applies subject matter knowledge.
* Primary responsibility is ensuring implementation of quality plan and quality assurance regulations at every stage of the Clinical Trial process.
* Write and revise SOPs.
* 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.
Real is part of the larger SThree K.K group
To find out more about Real, please visit www.realstaffing.com | Real についてもっと詳しく知りたい方はこちらへ→ www.realstaffing.com
Award winner of:
Great Place to Work 2019 | Growth Company of the Year by TALint Recruitment Awards 2019 | Best Healthcare & Life Sciences Recruitment Company of the Year by Recruitment International Awards 2018
- 応募資格
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- 必須
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1.Individual contributor that works under limited supervision.
2.Applies subject matter knowledge.
- 歓迎
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1.Major in related Field of Study or Associates Degree (± 13 years)
2.Native level in Japanese
3.Business level proficiency in English(Reading and Writing)
- フィットする人物像
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<Qualifications>
1 Major in related Field of Study or Associates Degree (± 13 years)
2 Native level in Japanese
3 Business level proficiency in English(Reading and Writing)
- 雇用形態
- Permanent
- 勤務地
- Chiba
- 年収・給与
- JPY9,000,000.00 - JPY11,000,000.00 per annum + competitive