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Responsibility: Develop the products of sustained & controlled release oral solid dosage form including formulation & process development, technology transfer, scale-up and manufacturing of application batch, ANDA submission etc.


Qualification: Above 3 years of formulation ANDA submission &QBD prescribing studies experience in sustained release oral solid dosage form. Be familiar with technical requirement and procedure of R&D. Have good ability in formulation development and bibliographic search. Have good ability in communication and solution.