1. To ensure the compliance of SOP’s. 2. Lay down specifications and standard testing procedures for RM, PM, In-process, Finished products in co-ordination with production, QA, R&D & Purchase. 3. Evaluation of sampling procedures & instructions for RM, PM, In-process, Finished products. 4. Evaluation of test procedure for RM, PM, In-process, Finished products. 5. Review of protocols, reports, data of validations for new developed analytical method, verifications of pharmacopeial products & method transfers. 6. Laboratory management in line with GLP. 7. Ensuring smooth functioning of all instruments & plan for all the routine day to day analysis. 8. Carry out stability studies for all API's as per the protocol and schedules. 9. Initiate & investigate the OOS for non- conformities. 10. Evaluate all the sub-ordinates on the performance. 11. Review and Approval/ Rejection of all Raw Materials, Packaging Materials, Intermediates, In-process materials and Finished products. 12. Giving analytical support for Process and cleaning validations. 13. Laboratory investigation on customer complaints and OOS. 14. Responsible for the password policy. 15. Responsible for periodical monitoring of audit trials. 16. Handling of Reference & Primary and Working standards. 17. Handling of GC & HPLC instruments and their columns. 18. Responsible for the calibration of Instruments HPLC, GC, IR, UV etc. 19. Handling of left over samples as per the procedure. 20. Initiating the lab incidents related to quality control and closing with proper investigation. Proposing CAPA with proper justifications. 21. Preparation of samples and reports for potential customer. 22. Responsible for the batch release. 23. Daily monitoring of water analysis and review of data generated. 24. Ensuring continuous safety procedures in Quality control department. 25. Indenting and Approving (if required) QC Indents and follow up with Purchase Department. 26. Verification of COA's for Raw Materials, Packing Materials, Intermediates and Finished products. 27. Handling of Risk Management, Out of Trend & Out of Calibration. Job Types: Full-time, Permanent Pay: ₹150,000.00 - ₹200,000.00 per month Benefits: Cell phone reimbursement Health insurance Leave encashment Provident Fund Work Location: In person
1. To ensure the compliance of SOP’s. 2. Lay down specifications and standard testing procedures for RM, PM, In-process, Finished products in co-ordination with production, QA, R&D & Purchase. 3. Evaluation of sampling procedures & instructions for RM, PM, In-process, Finished products. 4. Evaluation of test procedure for RM, PM, In-process, Finished products. 5. Review of protocols, reports, data of validations for new developed analytical method, verifications of pharmacopeial products & method transfers. 6. Laboratory management in line with GLP. 7. Ensuring smooth functioning of all instruments & plan for all the routine day to day analysis. 8. Carry out stability studies for all API's as per the protocol and schedules. 9. Initiate & investigate the OOS for non- conformities. 10. Evaluate all the sub-ordinates on the performance. 11. Review and Approval/ Rejection of all Raw Materials, Packaging Materials, Intermediates, In-process materials and Finished products. 12. Giving analytical support for Process and cleaning validations. 13. Laboratory investigation on customer complaints and OOS. 14. Responsible for the password policy. 15. Responsible for periodical monitoring of audit trials. 16. Handling of Reference & Primary and Working standards. 17. Handling of GC & HPLC instruments and their columns. 18. Responsible for the calibration of Instruments HPLC, GC, IR, UV etc. 19. Handling of left over samples as per the procedure. 20. Initiating the lab incidents related to quality control and closing with proper investigation. Proposing CAPA with proper justifications. 21. Preparation of samples and reports for potential customer. 22. Responsible for the batch release. 23. Daily monitoring of water analysis and review of data generated. 24. Ensuring continuous safety procedures in Quality control department. 25. Indenting and Approving (if required) QC Indents and follow up with Purchase Department. 26. Verification of COA's for Raw Materials, Packing Materials, Intermediates and Finished products. 27. Handling of Risk Management, Out of Trend & Out of Calibration. Job Types: Full-time, Permanent Pay: ₹150,000.00 - ₹200,000.00 per month Benefits: Cell phone reimbursement Health insurance Leave encashment Provident Fund Work Location: In person