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| 部署・役職名 | Regulatory Affairs Manager |
|---|---|
| 職種 | |
| 業種 | |
| 勤務地 | |
| 仕事内容 |
You will be in charge of making the plan to get our medical devices approved for sale in Japan. This means you will manage the official paperwork and talk regularly with Japanese government groups to get the approvals. Responsibilities － Create and follow a smart plan to get products approved. － Explain complex rules and ideas in a simple, clear way. － Work well with government officials and company partners. － Talk with the government to find the best solutions for the company. － Make sure the company follows all Japanese laws for medical devices. |
| 応募資格 |
【必須（MUST）】 － Degree and at least three years of experience with medical device rules.－ Fluency in Japanese with business－level English. － Good communicator, especially when talking to the government. － Strong skills in thinking carefully to solve difficult problems. － Be able to work hard by yourself and handle many tasks at one time. |
| 受動喫煙対策 | 屋内禁煙 |
| 更新日 | 2025/11/17 |
| 求人番号 | 6127568 |
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- 会社規模101-500人
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転職・求人情報の詳細をご覧になる場合は会員登録（無料）が必要です