<ul><li>Design and execute formulation development trials for various dosage forms such as tablets, capsules, powders, liquids, and injectables.</li><li>Conduct pre-formulation studies and compatibility studies of APIs and excipients.</li><li>Optimize formulation and manufacturing processes using QbD principles and statistical tools like DoE.</li><li>Prepare and review technical documents including formulation development reports, MFR, BMR, and technology transfer documents.</li><li>Coordinate with Analytical R&amp;D for sample testing and stability studies as per ICH guidelines.</li><li>Participate in scale-up, exhibit, and validation batches in coordination with production and quality teams.</li><li>Ensure adherence to cGMP, GLP, and regulatory standards during all R&amp;D operations.</li><li>Support regulatory dossier preparation by providing technical data, development rationales, and process justification.</li></ul>

FR&D Executive