Plan and executeproduct development activitiesfrom concept stage to commercialization as per market and IP requirements. Supportplanning, budgeting, and lifecycle managementof FRD projects. Ensure all development activities comply withcGMP and GLP guidelines . Maintain development documentation includingMFR/MFC logs, product codes, and equipment records . Coordinate withcross-functional teams (QA, QC, RA, Production, Supply Chain)for smooth project execution. Monitorequipment qualification activities (IQ/OQ/PQ/CQ)and maintain SOP compliance. Manageprocurement of materialsrequired for development trials from warehouse or vendors. Reviewtest protocols, reports, batch records, and development documents . Participate in investigations related toOOS, OOT, deviations, change control, and root cause analysis . Support preparation ofProduct Development Reports (PDR)and regulatory documentation. Monitorscale-up batches, process validation, and commercial validation batches . Ensure smoothtechnology transfer from R&D to manufacturing . Coordinate with vendors foroutsourced testing and technical activities . Supportregulatory query responses and auditsas a Subject Matter Expert (SME). Ensure compliance withhealth, safety, and environmental standards .
Job Title
Formulation Scientist