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.