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）

Assist in formulating Compliance policies

Degree in Business Administration, Law, or related

Good command in English and Chinese

Assist in formulating Compliance policies

Degree in Business Administration, Law, or related

Experience in regulatory compliance preferred

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

Degree in Business Administration, Corporate Governance, Law preferred

Experience in regulatory compliance preferred

Holder of Enhanced Competency Framework Certifications (e.g. ACOP) preferred

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

Assist in overseeing regulatory-related projects, ensuring compliance and timely delivery.

Maintain close communication with regulatory authorities, preparing and reviewing documents.

Bachelor's degree required, at least 3 years of project management experience preferred.