Registered Pharmacist | GMP Compliance | Quality & Ops | Tai Po Site

Description: Assist in ensuring that pharmaceutical products are manufactured, tested, and released in full compliance with Good Manufacturing Practice (GMP) requirements Support the Authorized Person (AP) in the certification and release of pharmaceutical batches, ensuring compliance with registered product particulars Gain hands-on exposure to quality control activities, including sampling, testing, analysis, and related documentation Assist in the preparation, review, and maintenance of Standard Operating Procedures (SOPs), batch manufacturing records, and validation protocols Participate in GMP audits, compliance reviews, and process improvement initiatives under the guidance of the AP or senior management Develop a practical understanding of Hong Kong pharmaceutic

Location: Hong Kong SAR

Posted on: 08-Jan-2026