Responsibilities：

1.Coordinate analysis group member, work schedule and manage analysis procedure, ensure right data can be provide in time.
2.Contact with other departments; check the work schedule to ensure it can meet all the analysis task (including validation, water inspection, environment / person sanitation etc.)
3.Check all the report including analysis report.
4.Provide product quality trend, quality alert, and suggestive relative necessary measurement to reduce the quality risk.
5.Ensure reasonable use of QC apparatus and reagents, and give the monthly demand.
6.Responsibility of management guidance and training of the analyzer, train the new personality.
7.Responsibility of EHS audit and assessment of the analysis field, work quality and enforcement of GMP and SOP, give the approach if problems appear.
8.Responsibility of the roll book and monthly report.

Qualifications:
1.University and above in pharmaceutical chemistry, pharmaceutical analysis or biological.
2.Above 5 years relative work experience, at least 4 years quality field management experience.
3.Knowledge of state and local quality policy procedure (GMP, GLP, DII, DCI etc.)
4.Familiar with lab quality specification and procedure, and current CNP, international universal specification such as USP, EP.