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Responsibility: Development and validation of analytical methods of sustained & controlled release oral solid dosage form products, conduct stability studies and formulation testing etc. Complete of analytical section in regulatory file, and support to file dossier.

Qualification: Above 3 years of work experience in analytic development. Be familiar with analytic regulation, technical requirement and analytic instrument include HPLC, GC, Mass Spectrometry etc. Have good ability in communication and solution.