· 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.