Ensure operations meet ISO 13485, CE Mark, FDA 510(k), NMPA requirements

At least 8 years experience, 3+ years QA leadership in medical devices

Fluent in English, Cantonese, and Mandarin required

至少3年藥品註冊工作經驗，具備東南亞國家註冊成功案例者優先

熟悉越南、泰國、馬來西亞、印尼等國的藥品註冊流程與法規要求

彈性工作安排（可選擇全職或兼職）

相關學科學士學位要求

監管合規經驗優先

ACOP認證優先考慮

Experience in regulatory compliance preferred

Degree in Business Administration, Law, or related

Good command of English, self-motivated, excellent communication skills

Supports governance and operations in Information Technology Department

Bachelor's degree in Business Administration, IT, or related field required

Minimum 2 years' experience in IT asset management or compliance

Build and execute global regulatory strategy

Experience with FDA, NMPA, MDR a plus

Bachelor's degree in Life Science, Biotechnology, Engineering

Assist in formulating Compliance policies

Degree in Business Administration, Law, or related

Good command in English and Chinese

5+ years BA/PM experience in large investment banks

Advanced SQL & Excel Macro skills

Deep knowledge of Corporate & Investment Banking products

University degree in Business Administration, IT or related field

Minimum 2 years experience in IT Asset Management or related domain

Strong skills in Microsoft Excel, Visio, and PowerPoint