Major Accountabilities

• Perform the relevant Analytical testing (product/incoming material testing, stability testing, validation testing, and compliant sample testing, method verification/validation testing, cleaning validation testing, etc.), and provide the testing result in time.
• Execution of assigned tasks in the quality control laboratory in accordance with cGxP regulations. Performance of laboratory specific activities such as maintenance, calibration and qualification of analytical equipment.
• Participate in the establishment, implementation and maintenance of the quality system in lab, and support the strength of lab quality system and processes continually.
• Support for investigation related to deviations, OOS/OOE and complaints on analytical topics
• Provides the analytical techniques knowledge and expertise to support QC initiative in quality, compliance and efficiency continuous improvement.
• Comply with all HSE guidelines; Detect and report potential accident, risks and propose solutions
• Responsible for participating in initial training and retraining. Ensure all activities in compliance with cGxP, incl. data integrity

What you’ll bring to the role:

• Bachelor Degree in chemistry, pharmacy, biology or equivalent education
• 1-2 years of experience in pharmaceutical industry and/or analytical laboratory in GMP environment desirable
• Language: fluent in Chinese (Oral and written); Basic in English(Oral and written)
• Technical Skills on Laboratory equipment; Quality Control Testing; Quality Control Sampling;
• Collaboration; result-oriented; Breakthrough Analysis; Being Resilient; Operational Excellence; Continuous Learning;