Research Associate

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

Work Experience

M.Pharm. with 1-2 Yrs./

M.Sc. with 2-3 Yrs.