Urgent Opening for "Lab Chemist" ( QC/ Production) for leading Pharmaceutical company in kolkata (West Bengal)

SPEARHEAD- YOUR CONSULTING PARTNER IN HR & EDUCATION - Date posted: 31 Aug 2018
***Urgent Opening for "Lab Chemist" (QC/ Production) for leading Pharmaceutical company in kolkata***   salary for freshers is =4500-5000 + Free fooding & lodging Salary for Experienced candidate is = 8000-30000 +Free fooding & lodging   ***FRESHERS & EXPERIENCED BOTH CANDIDATE CAN APPLY. ( B.SC/ M.SC in chemistry/ zoology/B.Pharma/ M.Pharma/ biochemistry/ microbiology /botany candidate can apply...male candidate is preferable...!!!***   immediate joining   Department: **Q.C. / Q. A. / ANALYTICAL & PRODUCTION CHEMIST**   Job Responsibilities are: -   1. All the instruments handling, including HPLC, spectrometer etc., and its logbook preparation and maintenance. 2. To conduct the Stability Studies and assure the shelf life of the products. 3. To conduct the training programmed of the juniors on a regular intervals. 4. To conduct and overview of microbiological jobs for smooth running of Production. 5. To conduct the validation job, both in Mfg. process and analytical method validation. 6. Have to control over the Chemical, Microbiological, Instrumental tests conducted by all the Chemists. 7. Arrange all the documents to be made as ready reconer and recorded in the computers. 8. Daily reporting and MIS should follow on regular basis. 9. Complain handling and product recall procedure to be maintained. 10. Proper Computer handling. 11. Analytical method development both existing and new products and it’s validation. 12. All the necessary activities to be done for getting WHO GMP certificates for up gradation of our Industry in respect of Quality and Quantity. 13. Operational improvement on G.M.P and G.L.P & ISO / WHO related affairs and thereby set/reset the requisite formats & projects duly prepare and its implementation. 14. To coordinate with all the development work related product development and its proper implementation. 15. Preparation of advance production planning daily and its implementation. 16. Records for validation of system for treatment of water to render it potable & total water system validation. 17. Monitoring and implementation of the documental records to be prepared by Q.C. Department for authorization and detailed specification for – a. All materials ii) Regents iii) Solvents & iv) Water. 18. Complain investigation recording format and its proper implementation. 19. Specification records to be prepared for: i. Raw Materials. ii. Packing materials. iii. For Product containers and closures. iv. For Finished Products. 20. Up-gradation of Master formula records. 21. Up-gradation of batch processing records. 22. Preparation of S.O.P.S for: i. Receipt of raw material ii. Sampling iii. Batch numbering iv. Testing v. Records of analysis. 23. Various procedures duly approved and validated for reprocessing and recoveries. 24. Preparation of predetermined protocols to be prepared for validation. 25. Records and SOP’s for routine Sanitation & Hygiene programmer to be drawn for compliance. 26. Records to be prepared at the time of each manufacturing operation. 27. You have to find out the sources of quality variation of the products either due to: i. Materials or ii. Machines or iii. Method of processing or iv. Men 28. Preparation of new formats and its implementation as per requirement of G.M.P & G.L.P which are mandatory but not yet introduced, to be introduced after the discussion with the Management. 29. You have to review the daily production records prepared by production departments and if there are any discrepancies, please feel free to discuss with concerned persons and inform to the management. 30. On line BMR is to be continued. 31. Daily inspection reports to be made & mail to HO mentioning the total item wise production, stage of semi finished product, packing etc. 32. Monitoring and reviewing all the documents & records done by Q.A / Q.C / Store pertaining to production, maintenance, quality control and dispatches.   Protocol Preparation, Review & Execution of – Process Validation, Cleaning Validation, Water System Validation, HVAC System Validation, Preservative Challenge Test, Validation / Qualification of Instrument / Equipments, and much more. ***CONSULTANCY TERMS & CANDITION IS APPLICABLE****    ...

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