1) Pharmaceutical product development from pre formulation, various drug delivery technologies, formulation, process & scale up manufacturing towards commercialization.
2) Guiding a team of scientists to develop various dosage forms for regulated/semi-regulated/other markets on time. Implementation of stability studies as per ICH guidelines.
3) Supervision and execution of manufacturing of Pre exhibit/ Exhibit batch which is manufactured at GMP location along with tech-transfer Manager. Monitor the equipment maintenance at the Advent Research Centre.
4) Preparation and evaluation of certain submission documents like Product Development Report (PDR), Master Formula Record (MFR) etc.
5) Guiding Documentation team for preparation of documents like status charts in excel, word documents, submission documents Master Formula Record (MFR), Product Development Report (PDR).
6) Approving art work. Monitoring the implementation of SOPs related to the department.
7) Monitoring and execution of all activity related to formulation development at the Advent Research Centre.
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