仕事概要
| 職種 | 技術職（販売、設計、開発、生産管理）／開発、研究、実験、プロジェクトマネージャー |
|---|---|
| 業種 | 医療／ 医薬品 |
| 雇用形態 | 未分類 |
| ポジションレベル | 本部長/経営層レベル |
| 募集人数 | 1名 |
| 希望入社時期 | - |
| 必須語学力 | |
| 活かせる語学 | - |
| 福利厚生・休暇 |
仕事詳細
Senior Regulatory Affairs Specialist, Medical device
- A leading US healthcare MNC
- Regulatory Affairs responsibility for Singapore and selected regional countries
Our client is a leading healthcare MNC with a global business in medical devices and consumables.
An exciting opportunity exists as a Regulatory Affairs Specialist responsible for medical device registration for Singapore and 1 or 2 other selected countries. The incumbent would be a key member of the regional regulatory team and reporting into the RA Manager. He/she will also be involved in product listing, delisting, reporting of adverse events, review change control requests, labelling change requests and submit all activities with authorities and the regional team’s requirements.
To qualify you would have a relevant degree in life science or in a related biomedical subject and will have a minimum of 2 years of experience in regulatory affairs. Experience in regulatory affairs within the medical device industry is preferred. You would have excellent understanding of the regulatory framework for medical devices in the region and an understanding of quality systems regulations, recalls and correction and labelling requirements. You would have strong oral and written communication skills.
面接について
連絡先
Senior Regulatory Affairs Specialist, Medical Devices
RGFタレントソリューションズ株式会社
40000 〜 60000 SGD
