Executive

Job Description

• Comply with all cGMP, GxP, or any other regulatory requirements, including EH&S requirements.
• Complete training on relevant SOPs and develop an understanding of the activities to be conduct prior to undertaking any task.
• Conduct all tasks/ activities as per applicable SOPs, report any difficulty or deviation in following the procedures/instructions to immediate Supervisors/Managers.
• Report any quality concerns or suggestions for improvements to supervisors/ Managers.
• Sampling, analysis reporting and deposition of raw material injectable Raw material as per standard test procedure. Disposition of analyzed samples after analysis and final approval.
• To ensure the OOS & OOT result communicates to concern person.
• Sampling kit maintenance.
• To perform routine calibration of instruments/ equipment.
• Review of documents related to quality control against the standard procedure e.g.: analytical raw data and calibration data etc.
• To record and ensure the SAP entries of Raw material.
• Disposition of left over samples.
• Maintaining the sampling booths in warehouse.
• To initiate and investigate the laboratory incidents.
• Any other assignment allocated by the section in charge / department head.
• Filling of analytical records and submission to Doc-cell ( as per applicability)
• Planning and co-ordination of Raw Material, execute and supervise all tasks and activities per the applicable SOPs.
• Authorize to print e-TDS from SAP for all type of QC samples.Reporting of event and abnormalities with preliminary investigation findings to Reporting manager, HOD’s, functional heads, event investigation team, EHS department’s managers and location head.

Work Experience

4 to 8 years

Education

Competencies