- 負責產品取證與國際法規申請(TFDA、FDA、CE) - 協助撰寫醫療軟體/AI產品相關法規文件 - 協助追蹤各國醫療法規與送審資料準備 - Handle certifications (TFDA, FDA, CE, etc.) - Prepare regulatory documentation for software/AI medical devices - Track global regulations and support submission
待遇面議
(經常性薪資達 4 萬元或以上)
• ▍必要條件 Requirements - 熟悉 ISO 13485、IEC 62304、SaMD 規範 - 有送審與撰寫技術文件經驗 - 具良好中英文書寫能力 - Knowledge of ISO 13485, IEC 62304, SaMD - Experience in submission and technical writing - Strong bilingual (Chinese/English) writing skills • ▍加分條件 Preferred - 具顧問或內部法規專職經驗 - 熟 FDA 南亞國家法規者尤佳 - Experience in regulatory consulting or in-house RA - Familiar with FDA and Southeast Asia regulations
1.Employee compensation and year-end performance bonus 2.Labor insurance, national health insurance and labor pension 3.Employee group insurance and free group insurance offered to employee's spouse and child(ren) 4.Regular health checks 5.Gift vouchers for birthday, childbirth, Spring Festival, Dardon Boat Festival, and Mid-Autumn Festival; and marriage and funeral grants 6.Annual company trip/ trip grant 7.New employee orientation and training; on-the-job education and training; and comprehensive career plan services 8.Bilingual Training