募集要項
- 募集背景
- A global medical device company is searching for a Regulatory Affairs Specialist. In this position, you will work with a growing team to ensure successful local regulatory filing and registration. This is a great opportunity to advance your career with an international company.
- 仕事内容
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A global medical device company is searching for a Regulatory Affairs Specialist.Responsibilities:
* Complete regulatory applications for the company's medical devices
* Develop regulatory strategies that ensure quick clearance
* Exchange information with international engineering and regulatory affairs organisations
* Liaise with regulatory groups
* Collaborate with laboratories to perform certification tests
* Act as consul to internal departments on local regulatory affairs
Requirements:
* Bachelor's degree or above
* 3+ years of experience in regulatory affairs for a medical device company
* Strong understanding of local regulatory submission requirements for medical devices
* Proficiency in Microsoft Office
* Ability and willingness to travel abroad occasionally
* Fluent level verbal and written Japanese; written and verbal English proficiency
- 応募資格
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- 必須
- 3+ years of experience in regulatory affairs for a medical device company
- 歓迎
- 英語力必要。その他は詳細からご確認ください。
- 雇用形態
- Permanent
- 勤務地
- Tokyo
- 年収・給与
- JPY5,000,000.00 - JPY7,000,000.00 per annum
- 休日休暇
- 完全週休2日制, 土日祝日休み, 有給休暇