·      Conducts intellectual searches for technical information through a variety of resources, including the online literature.

·      Active and inactive raw material sourcing and identification.

·      Develops and/or performs all formulation requirements on new formulas; includes creation of theoretical formulation, batch mixing development, and finished product specifications.

·      Filing of description/formulation sheet, performing lab tests, stability testing/ monitoring, and color verification, etc.                           

·      Participates in process improvement and product investigations and troubleshooting.

·      Reformulate to improve existing products as needed.   

·      Develop robust formulations and processes for immediate release and modified release tablet and capsule dosage forms.       

·      Scale-up and optimization of manufacturing process; execution of approved and developed batches; scale up and technology transfer from R&D to production to meet timelines.

·      Supplying the registration department with deficiency litters including: samples of newly approved formulas for registration, justification of certain specifications of the formula, and technical files.

·       Supplying QC department with verification samples at zero time for development of analytical methods, standards and finished product specifications for preparation of STP’S.

·      Supplying QA department with drug master formulas.

Skills

1. Hold a bachelor's degree in pharmaceutical science.  

2. Have 2-5 years of experience in the research and development-formulation department.