QC supervisor
(ICBR) International Center for Bioavailability and clinical Researsh
Total years of experience :19 years, 0 Months
1. Preparation of method development, Validation and Reports.
2. Data evaluation to achieve the acceptance criteria and suggest the samples that should be reanalyzed.
3. Supervise sample extraction and evaporation and correct sequence of injection, while maintaining instrumental conditions stable and correct. Print out chromatograms of the injected runs.
4. Manage the progress of work in the station.
5. Writing the analytical report and give it to the analytical division head to revise.
6. Record raw data promptly and accurately and in compliance with the principles of Good Laboratory Practice and Report deviations and problems to the Analytical division head, and define areas of weakness and propose solutions to enhance the work.
7. Enter the data to the volunteer validated excel sheet and print out the results to be placed clearly in the logbook.
8. Prepare working standard solutions and plasma calibrators and Quality control samples and prepare the mobile phase including pH adjustment and filtration .
9. Train and supervise the analysts
10. Write the Drug Specific Analytical Method Instruction
11. Ensure the safety practice in the laboratory.
12. Coordinate with analyst to sustain the supply of HPLC grade chemicals and solvents, by reporting the needs to analytical division head.
excellent
good grade