- To conduct literature search and prepare of the literature review presentation.
- To participate in the patent evaluation, non-infringing formulation report and get it transparent from IPR & Quality depts.
- To conduct the preformulation study for the product development.
- To prepare prototype formulations based on the preformulation study.
- To conduct the API characterization, compatibility study and recording the same in the lab book.
- To conduct development trials, achieving desired dissolution profiling and manufacturing the stability batches & bio equivalent batches.
- To evaluate the trials,bio-equivalence, and stability data scientifically & planning experiments.
- To participate in the exhibit batches
- To provide technical support in the Commercial batches as and when required.
- To optimize formulation process using DOE approach.
- To do the risk assessment of stability, excipients and processes.