Quality Control Analyst I

Watson Pharama

7 - 12 years

9 - 14 Lacs

chennai

Posted:1 day ago| Platform:

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Skills Required

selection process usage sap quality control analyst pharma analytical glp data integrity hplc recruitment

Work Mode

Work from Office

Job Type

Full Time

Job Description

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 softwares.
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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