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Teva Quality Control Analyst India, Tamil Nadu, Chennai 210578535
Yesterday
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How you’ll spend your day
- To perform Stability analysis.
- Maintenance of operating instruments / equipment.
- To maintain the assigned Laboratory workplace, instruments and equipment etc.
- To adhere Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure.
- Responsible for handling , operating and maintaining HPLC / UV and related instruments to ensure optimal performance.
- Adherence to Good Laboratory Practices (GLP), Good Documentation Practices (GDP), relevant regulatory guidelines and PAL procedure.
- Performing stability testing (Assay, RS & Dissolution) of all formulations by HPLC and UV techniques.
- Preparing samples and executing the same as per the Method of Analysis and Verification of sample set sequence in applicable software’s.
- Interpreting chromatographic data and ensuring proper documentation of all analytical activities in compliance with GLP / GDP requirements
- Reporting of interpreted data in line with specification, compliance and regulatory standards and maintaining data integrity throughout the analytical lifecycle.
- Evaluation of reported results and reporting of any abnormal results to the supervisor ontime.
- Handling of laboratory software's.
- Ensure to use safety apparels and PPEs while working in the laboratory.
- Ensure timely completion of assigned training.
Your experience and qualifications
- M.Sc., Chemistry
- 7+ years of experience
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