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About the role
Role & responsibilities : Support technology transfer from R&D to commercial manufacturing. Monitor manufacturing processes and identify opportunities for process improvement. Review Batch Manufacturing Records (BMR), Process Flow Diagrams (PFD), SOPs, and process documentation. Assist in process scale-up, trial batches, exhibit batches, validation batches, and commercial batches. Participate in Process Validation, Equipment Qualification (IQ/OQ/PQ), and Process Verification activities. Investigate process-related deviations and support Root Cause Analysis (RCA) and CAPA implementation. Coordinate with cross-functional teams including Production, QA, QC, Engineering, and Warehouse. Prepare and maintain process-related documentation, validation reports, SOPs, and change controls. Ensure compliance with cGMP, regulatory guidelines, EHS, and Data Integrity requirements. Support continuous improvement initiatives to enhance productivity, yield, and operational efficiency Preferred candidate profile Designation : Officer/Sr. Officer Location: Vadodara,Luna, Padra Gujarat Department: Process Engineering Employment Type: Full-Time Industry: Pharmaceuticals, Only API Experience: 25 Years Education: B.E./B.Tech (Chemical Engineering)