Quality Control Supervisor

 Review and check the raw data generated under his supervision.
 Plan and distribute the daily routine work.
 To assist analyst for trouble shooting of instrumental problems.
 To ensure availability of reference and working standards.
 To ensure that all instruments are calibrated as per schedule.
 To maintain instrument parts, columns, etc.
 Review and maintain the logbooks, COAs, specifications and test procedures related to his section responsibility.
 Analysis and approval of cleaning validation / verification samples.
 Release/Rejection of products and materials and issue of release or rejection labels.
 Approving of receiving logbook.
 Report to QC Manager about the out of specification results obtained in routine analysis and retesting in order to perform proper investigation to verify the deviation.
 To ensure the approved procedures and specifications are followed.
 To check the artwork forwarded by R&D.
 Perform proper training for employees.
 Perform trend analysis.
 Signing off on COA etc.
 To ensure availability of adequate media, reagents, glassware and solutions.
 To ensure preparation and sterilization of media and documentation for preparation of media as per designed procedure.
 To ensure proper maintenance of media stock.
 To ensure disposition of samples and used media.
 To perform developmental activities.
 Maintain proper control for raw material supplier’s qualification program.
 Performing required risk approach for all critical tests (Heavy metals, Residual Solvents ,…etc.).
 To be aware about pharmacopeia analytical requirements.
 Has long experience for different analytical techniques.