1. Final Review of all the documents of Total Quality Management Systems (TQMS) related to Pharmaceutical, FMCG and Herbal Products. 2.Review of data related to Regulatory affairs of Pharma and FMCG products. 3. Reply for the Market Complaints of FMCG products. 4. Final Review of all the analytical data.related to Pharma and FMCG. 5. Preparation of Specifications for all the Raw Materials and Finished Goods of FMCG and Pharma products. 6. Writing and review of Operational and Calibration SOP's of all the analytical Instruments. 7. Writing and review of all the SOP's required for cGMP compliance related for Pharma and FMCG products. 8. Final review of all the ARTWORK of FMCG Products for Indian and Global markets. 9. Writing and review of Specifications for Herbal extracts. 10. Writing and review of Analytical Standard Test Procedures related to Pharma and FMCG products. 10. Writing and review of