Job Description

Long Description Supervise compliance to all CGMP, GXP or any other regulatory requirements, including EHS requirements. Complete self-training and monitor training of team members on the relevant SOP. Execute and supervise all tasks and activities as per the applicable SOP. To ensure instrument s, equipment s are calibrated, qualified before starting the analysis. To ensure online entry of instruments, Working, Reference Standard and timely updation in log. To ensure error free documentation and Self review of analytical results with raw data before submitting for final review. To ensure that specification, used glassware, columns are kept in the designated place after use. Responsible for timely analysis and reporting of allotted samples as per approved or current specification and TSTP, FPSTP. Interpretation of analytical data, recording of critical observations during analysis, reporting and co-relating observations with the results obtained. Review of analytical reports with raw data and filling in relevant files. Responsible for immediate reporting and discussion of Incident if any. To ensure that analytical solutions are retained till completion of calculation and documentation to facilitate the investigation procedure. To implement corrective and preventive actions identified during the investigation. To ensure sample destructions after completion of entire analysis as per the relevant SOP. To report any quality concerns or suggestions for improvement to respective Managers. To do sample entry and allocate A. R numbers to samples. Issuance of TDS for analysis and preparation of CoA. Any additional responsibility delegated by section head or department head. Competencies Education Post Graduation in Analytical Chemistry or Pharmaceutical Chemistry Masters in Organic Chemistry or Science Work Experience M. Pharm. with 1-2 Yrs. / M. Sc. with 2-3 Yrs.