RM, Documentation, Validation .1. To plan, execute and review daily routine activity of Raw material, Blend, Uncoated tablet, Coated tablets, Filled capsules, Finished products and Stability samples by physical, chemical and instrumental testing as per approved procedure and prepare report. 2. To prepare and review QC documents such as specifications, standard test procedures, standard operating procedures, certificate of analysis etc. 3. To plan and execute analytical method validation and maintain the record. 4. To participate in validation process such as process validation, cleaning validation, equipment/instrument qualification, analyst qualification and maintain the record. 5. To receive and maintain the control sample of raw materials and finished product and record. 6. To report and investigate any incident, deviation, OOS (Out of Specification) and OOT (Out of Trend). 7. To initiate and report any change control and CAPA. 8. To Review laboratory solution as per requirement. 9. To Review of standardize volumetric solution. 10. To prepare working standard and maintain the record of working standard, reference standard and impurities. 11. To maintain the instruments in proper conditions and to report any problems or errors. 12. To maintain all records relevant to the work, instrument and equipment for each operation in neat and good conditions. 13. To follow the Good Laboratory Practices in the work. 14. To monitor department cleaning activities. 15. To carry out calibration of laboratory instrument and Review as per frequency and maintain records. 16. To send the samples for outside testing laboratory and follow up for testing and result. 17. Any other work assigned by superior. 18. To allocate work distribution. 1. To plan, execute and review daily routine activity of Raw material, Blend, Uncoated tablet, Coated tablets, Filled capsules, Finished products and Stability samples by physical, chemical and instrumental testing as per approved
