1. To ensure the analysis of the in process product or finish product sample and on time and release of it as specified under various regulatory norms and in house standards.2. To prepare the working standards as per the guidelines and pharmacopoeias.3. To record all the data related to the testing online on day-to-day basis.4. To bring to the notice the abnormalities and deviations to Manager Quality Control.5. To perform the tests as per the specification & standard test procedure and record the necessary results in respective documents.6. To investigate failure of finished product (FP) or In-process (IP) product, in case of any out of specification (OOS) or Laboratory error or deviation and take corrective and preventive actions.7. To carry out the calibration of all the analysis instruments as per the schedule.8. To prepare reagents and volumetric solution and standardize it.9. To follow Quality Control SOPOnly Pharma & Science graduates can apply.10. To handle the instruments likes HPLC, UV, and Karl Fisher11. Responsible for qualification activities of all sophisticated instruments.12. Must have working knowledge of OOS, OOT, CAPA, Deviations, Change controls.Job Types: Full-time, Regular / PermanentSchedule:
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