- Stable and transient cell line development of lentiviral vectors (Transfections, Single cell sorting, Cell Bank generation)- LVV Upstream process development from clone stage to bench scale (2 L, 5 L) and process optimisation (AMBR-250)- Laboratory and warehouse management- Collaborations with in-house departments.and external partners- Planning and execution of the experiments/projects- Data presentation to large audience- Support in decision making with the base of scientific data, pitching in novel ideas in establishing new technology for process automation- Documentation adhering to cGLP principles, creation of reports and SOPs using softwares like LIMS, DocNET

- Scale Down Model Development in AMBR 15

- Cell culture process development using CHO and Hybridoma Cell lines at bench scale (3L) in GLP environment- Conduct bioreactor characterization studies (kLa, OUR etc.) in small scale (3L and 10L) and in mini-bioreactors (AMBR-15)- Application of DOE principles and multivariate data analysis by effective utilization of software like JMP- Experimental data analysis in drawing logical scientific conclusions- Preparation of technical reports and data summary documents

Production of biopolymer-based aerogels for different food applications via CO2 induced gelation. Aerogel properties like specific surface area and stability are optimized varying process parameters (temperature, pressure) and solution parameters (biopolymer concentration, composition).

- GMP CHO Cell culture manufacturing and primary clarification at 5 L, 200L and 1000L scales- Proficient handling, maintenance (CIP, PHT and SIP) and monitoring of large scale STRs using SCADA, and MCS control systems- Bioreactor characterisation (KLa study, mixing time study) at 1000 L scale- Media, buffers, feed and additives preparation using pressure vessels in cGMP conditions (Clean rooms)- Trouble shooting of process and equipment related problems in conjugation with Engineering department- Supporting initiation and closure of deviations from Standard operating procedures (SOPs) by Root cause analysis (RCA)- Coordination with Research and development, Quality Control (QC), Quality Assurance (QA), Warehouse and Engineering departments

Examination of Drug properties (purity, sample concentration, partial structure validation) and control it's quality using analytical techniques such as HPLC, GC, FTIR and UV-Spectrophotomer