Description: Lead and coordinate projects assigned by management, supporting continuous quality improvements; Develop, implement, and maintain quality management systems in compliance with regulatory standards (PIC/S GMP); Prepare for, participate in, and support internal and external audits; Manage regulatory affairs, including submissions and communication with authorities; Oversee all dangerous drug transactions within the operation site in line with legal and company protocols; Participate in pharmaceutical product development, from concept to launch; Report regularly to Head of QA / Authorized Person. Qualifications
Location: Hong Kong SAR
Posted on: 10-Jan-2026