【Foreigners Welcome】實驗室品管專員 (QC Chemist / Quality Control Specialist)

For candidates who enjoy laboratory work and aspire to build solid expertise in pharmaceutical Quality Control (QC)—we welcome you to join our team!

As a key member of our Quality Control (QC) team, your main responsibilities will include:

Testing & Record Management: Perform inspection, analysis, and documentation for raw materials, packaging materials, finished products, and stability samples.

Analytical Instrument Care: Execute daily checks, calibration, operation, and basic maintenance of analytical instruments.

Method Transfer & Validation: Support the execution of analytical method technology transfers and method validations.

GMP Documentation: Utilize, maintain, and update test records, specifications, analytical procedures, and related SOPs in compliance with the GMP document control system.

Inventory & Resource Management: Manage the requisition, inventory, and handling of reagents, reference standards, lab consumables, and test samples.

Quality Investigations: Assist in investigations and implementation of corrective/preventive actions for out-of-specification/out-of-trend (OOS/OOT) results, deviations, and non-conformances (CAPA).

Lab Maintenance & Operations: Maintain laboratory 5S standards, environmental cleanliness, and EHS (Environmental, Health, and Safety) compliance; complete other tasks assigned by supervisors.