# data[].attributes.body
►Patent, Pharmacovigilant Plan, and Biotechnology Developing

►QA, QC and Quality Specifications as per the requirements of Pharmacopeias and international regulation standards, like ICH
►GCP, GMP and GLP of pharmaceutical industry
►Project Management in Public Health.

# data[].attributes.body
►8+ years Research & Development experience in Biotechnology Industry, Medical Affairs, Clinical Trials, Registration, and Brand Maintenance

►All-round knowledge in Immunology, Bio-pharmaceutical products and the International Registration, like WHO prequalification

►Team work, honest & integrity and being flexible with conscientious characteristics under competitive working environment, conceptualized the strategic aims into the concrete working steps

►Fluent English and Mandarin capabilities, proficient in Microsoft Windows 7 and relate software, like MS Office; also familiar with Apple Mac system (iPAD, MacBook Pro).