Job Duties:

• Maintain GMP document system and updates the change control system.
• Perform line inspection, in-process control and sampling
• Prepare raw materials and packaging materials specifications
• Handle material defects reporting
• Provide quality related training and maintains the training data and record
• Prepare annual product quality review (APQR) report
• Coordinates with other departments on various aspects to ensure cGMP is followed

Job Requirements:

• High Diploma or above in science discipline, preferably in Pharmaceutical Science, Food Science or Quality Management aspects
• Fresh graduate is welcome; 1 year working experience relevant to GMP/ISO or other equivalent quality management system standards is a plus
• Experience in pharmaceutical industry is an advantage
• Good command of computer literacy would be required
• Proficient in both written & spoken English & Chinese
• Self-motivated and with good analytical mindset
• Candidate with less experience will be considered as Assistant, Quality Assurance

We are an equal opportunity employer and all information collected will be used for recruitment purpose only.