Group lead responsible for ideation, identification, development, technology transfer, scale up and commercialisation of all LARGE VOLUME PARENTRALS in sun portfolio.1. Product Ideation / Pre -PIF Evaluation Provide strategic inputs in Pre-PIF meetings/forums, to assure screening of appropriate product and accurate identification of related requirements. Propose estimated budget for development along with capex requirements.2. Formulation Development Strategy proposal, finalisation & ExecutionExplore and identify out-of-the-box solutions to meet innovation challenges in the process of complex formulations research. 3. Product Development/ New TechnologiesEnsuring the concept of “RIGHT FIRST TIME” for Every undertaken project. 4. Product Life cycle management and Regulatory SupportUse Lean principles in driving Product Life cycle management. 5. Intellectual Property Development & IP FencingGenerating sufficient IP barriers for protection of the product being developed in order to acquire greater market share.6. Futuristic Team building Identify and Mentor key talents in the FDD team . Utilization of technical skillsets within the team for development to ensure that the team is abreast of latest technologies and knowledge related to FDD.

Responsible for developing INFUGEM first oncology molecule in ready to infuse form with dose banded label. Responsible for Formulation development of Parenteral projects (505b(2)) and ANDA Projects. Drafting, Manage and Maintain the project budget and all project constraints i.e. time, cost, and quality standards. Providing technical inputs for Portfolio management of introducing and closing projects into development grid. Attend and lead periodic review meetings, daily huddles, monthly leadership reviews and monitoring progress and periodically provide project updates. Drafting, managing and approving all technical reports/submissions/fillings related to the projects. Familiar with project management tools (MS Office, MS Project, Primavera, Gantt charts, spreadsheets, ERP systems)

Formulation development of lyophilized injectables -

new liposomal project ideation. Preparing product proposals for new technologies and novel drug delivery systems. responsible for commercial batch manufacturing of liposomal drug delivery system for LIPODOX ( Pegylated liposomal doxorubicin) . Formulation development of hormonal lyophilized injectables. Lipid emulsion of propofol etc.

Working in LIPID RESEARCH Group responsible for scale-up of liposomal drug delivery system for LIPODOX ( Pegylated liposomal doxorubicin). Supervising commercial launch in INDIA and monitoring and supporting commercial batches manufacturing.

Working in LIPID RESEARCH Group responsible for formulation development of liposomal drug delivery system for LIPODOX ( Pegylated liposomal doxorubicin). As a core team member was responsible for process development, process optimisation, scale-up, manufacturing of clinical batches for INDIAN Market.

Oral and parenteral dosages forms. Responsible for literature search, formulation development, technology transfer, trouble shooting, documentation and presenting new project proposal

Formulation development of Oral drug delivery systems. Worked on liquid paediatric syrup, Tablet, and capsule dosage forms. Was responsible for preforming literature search, reports drafting, formulation experiments and analysis of same using different analytical techniques including HPLC, UV etc

Formulation Development Oral drug delivery systems . Response for Preformulation trials, stability batches of Tablets , Capsules, coating, IPQC, Documentation, SOPs, etc. Got extensive exposure to unit operations and equipments like RMG, Tablet Press, containment, GMP Documentations, Packaging lines .