Ryan Lee Email & Phone Number

I have about 10 years of experience in pharmaceutical industry with abundant experience in the areas of Quality Control (3 years), Analytical Research Development (4 years), and Quality Assurance (3.5 years) Achievement as an QA Specialist:Since I assumed my new position in QA in 2016, I was immediately in charge of the Deviation/LIR and CAPA system. With my strong English skills, I was put to review, revise or draft all deviation/ lab investigation reports. In past year I've prepared more than 30 reports with my strong analytical and critical thinking skills and the reports were written with concise and logical context to identify the root cause and to provide solutions. I was the key person to ensure all reports and documents meet the highest standards of FDA and/or our foreign clients, and I was also responsible for providing solutions to the questions and challenges raised by FDA and/or our foreign clients. Besides the investigations, I was also in charge of developing CAPAs that address the root cause identified. I also perform investigation for complaints to ensure all reported issues were addressed.

Listed skills include Pharmaceutical Industry, Gmp, Hplc, Chromatography, and 13 others.

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  University Of California, Davis

  Biotechnology