Xiaoxuan Guo

Pharmaceutical quality professional with 9 years of experience in pharmaceutical and traditional Chinese medicine quality control, GMP-compliant laboratory operations, analytical testing, documentation management, and quality system processes. Experienced in SOP management, deviation/OOS handling, analytical method verification, quality documentation review, and laboratory workflow improvement. With a strong interest in artificial intelligence applications in life sciences, I have independently explored AI-assisted solutions for pharmaceutical quality management, including documentation workflow optimization, knowledge management, and SOP information retrieval.

Seeking opportunities to contribute pharmaceutical expertise, analytical thinking, and AI-enabled process improvement capabilities in quality operations, life science technology, and healthcare innovation.

Quality Control Analyst at Hongzhengdao Traditional Chinese Medicine Research Co., Ltd. (2019-03 – 2023-05)

• Performed pharmaceutical quality testing and analytical evaluation according to GMP requirements.
• Conducted analytical testing using chromatography-based methods including HPLC, GC, and related laboratory techniques.
• Supported laboratory quality systems through documentation review, SOP compliance, and data integrity practices.
• Participated in investigation and evaluation of abnormal results, supporting OOS/deviation handling processes.
• Assisted with method verification, equipment management, reagent control, and laboratory workflow improvement.
• Maintained accurate records and ensured compliance with quality requirements.

Quality Control Analyst at Guangzhou Baiyunshan Zhongyi Pharmaceutical Co., Ltd. (2014-07 – 2019-03)

• Performed pharmaceutical quality testing and analytical evaluation according to GMP requirements.
• Conducted analytical testing using chromatography-based methods including HPLC, GC, and related laboratory techniques.
• Supported laboratory quality systems through documentation review, SOP compliance, and data integrity practices.
• Participated in investigation and evaluation of abnormal results, supporting OOS/deviation handling processes.
• Assisted with method verification, equipment management, reagent control, and laboratory workflow improvement.
• Maintained accurate records and ensured compliance with quality requirements.

Degree in Pharmaceutical Analysis – Guangdong Pharmaceutical University (2010-09 – 2014-06)