Highly self-motivated, well organized and professional process scientist with more than 16 years of experience in performing process development and scale up of variety of pharmaceutical products and experienced in developing the process for Oligonucleotide products. Looking out for great challenging position in the area of pharmaceutical field that utilizes skills and provides an opportunity for self and organization growth.
Responsible for project functions including managing team.
Evaluating and writing the Request for Proposal for the oligonucleotide molecules.
Preparing business case studies and market strategy for Oligonucleotide
Developing and transfer the technology to scale up and executing in the pilot scale for Oligonucleotide.
Responsible for preparing weekly updates, preparation of development report and Gantt chart preparations.
Evaluate tech-pack protocol and perform reactions on gm to Kg scale.
Preparation cost sheet and requesting to other cross-functional team to evaluate requirement such as reactors, QC requirements including stability as well as validation.
Co-ordination with CFT team includes Analytical, Process engineering, Process Safety and Quality Assurance to deliver project with timeline.
Preparing TTD report and sharing across through production and QA for BMR preparation.
Well knowledge in Solid phase Synthesis of Oligonucleotide with different type of modification (Like Conjugation, backbone and modified RNA & DNA.Syngene International limited is an ISO 9001:2008, ISO 14001:2004, and OHSAS 18001:2007 certified company having GMP facilities. Syngene is an internationally reputed custom research and manufacturing organization.
Worked as a Scientist in Sequent Scientific Limited,
Bangalore, India.
Worked as a R & D Research Executive in Orchid Chemicals & Pharmaceuticals Limited, Chennai, India.
Experiment Design