- Dossier extension of already developed formulations to global regulated markets of solid oral dosage forms.
- Formulation development, scale up and technology transfer of newly developed solid oral dosage forms & documentation thereof.
- Handling of equipment used for manufacturing of solid oral dosage forms at lab as well as commercial scale.
- Writing laboratory note books, scale reports, QbD based product development reports, submission batch reports, master formula card, process validation reports etc.
- Co-ordination within the team and with cross-functional teams and assist in regulatory query response as well as assist in product filing for ROW markets.