Description: Develop, implement, and maintain Quality Management Systems (QMS) in compliance with PIC/S GMP and applicable regulatory standards Prepare for, participate in, and support internal and external audits, including regulatory inspections Manage regulatory affairs activities, including dossier preparation, submissions, and communication with regulatory authorities Oversee and control all dangerous drug transactions at the operation site in accordance with legal requirements and company procedures Participate in pharmaceutical product development, supporting activities from concept through to commercialization
Location: Hong Kong SAR
Posted on: 08-Jan-2026