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ThePlacementGuru
Feb 19, 2019
Full time
Experience - 1-4 Years To carry out all activities in accordance with the GLP. Inward entry of samples/products/materials from production and stores. To carry out analysis of assigned in-process and finished products and stability samples. To carry out the chemical analysis of assigned product/ material within the stipulated time period. Prepare summary sheet of stability samples allocated by the supervisor. Prepare STP, SPEC and TDS of assigned products. Prepare documents related to work, as and when required. Carry out QC daily work reporting. Perform all lab work allocated by the supervisor. In the absence of the documentation personnel, all the responsibilities will be carried out by his/her designee, as directed by the supervisor.
ThePlacementGuru
Feb 19, 2019
Full time
Experience- 1-4 Years To carry out all activities in accordance with the GLP. Inward entry of samples/products/materials from Production. To carry out analysis of assigned in-process and finished products and stability samples. To prepare necessary documents related to the analysis samples assigned to the individual. Preparation and standardization of working standards and volumetric solutions. Calibrate Instruments and equipment, excluding the sophisticated instruments like HPLC, GC, AAS, UV-Visspectro photometer, as per their SOP’s. To carry out the chemical analysis of assigned product/ material within the stipulated time period. Perform all lab work allocated by the supervisor. In the absence of the chemical personnel, all the responsibilities will be carried out by his/her designee, as directed by the supervisor.
ThePlacementGuru
Feb 19, 2019
Full time
Experience- 3-5 Years To carry out all activities in accordance with the GLP. To carry out HPLC analysis of assigned raw material, in-process and finished products, and stability samples. Troubleshooting related to analysis on HPLC. To prepare necessary documents, including TDS, related to the analysis samples assigned to the individual. Calibration of Instrument/ Equipment as per respective SOP. Operation of HPLC, UV- Vis spectro photometer and any other instrument delegated by the supervisor. Preparation and standardization of working standard. Maintenance of HPLC and HPLC columns Perform all lab work allocated by the supervisor. In the absence of the chemical personnel, all the responsibilities will be carried out by his/her designee, as directed by the supervisor.
ThePlacementGuru
Feb 19, 2019
Full time
Qualifications - M.Sc./B.Pharma/M.Pharma Experience- 8-10 Years Planning and Execution of products required as per order received.·   Responsible for all manufacturing processes and solves the problems in batch of different manufacturing.·        Responsible for development of formulation of required product.·        Handling and improvement of formulation as per need of customer.·        Preparation and modification in standard operating procedure for the responsible section.·       Planning and Execution of Daily production targets.·        Verification of overall system of production and to submit the daily reports and statistics of production.·        Preparation and revisions of production MFC’s, BMR and SOP’s.·        Handling all the staff related to manufacturing, primary and secondary packing.·        quality control of all types of packaging material, printing
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