Working with Analytical devices.
Perform full raw materials and product tests such as determining the amount and determining impurities.
perform raw material and final product tests according to pharmacophe or internal methods.
perform assigned tasks According to the timed schedule.
Do teamwork for the Food and Drug Administration.
Perform stability tests. And internal.
Preparation of Quality Control Reports Includes: Analytics reports, analysis sheets and sustainability reports. Participation and analysis of out -of -range results and relevant reports. Analytics. Cooperation in laboratory documentation and guidelines.
Perform sampling of materials, products, packaging items and water consumed.
Update or suggest new and effective analysis methods.
Updates in the requirements and standards and updating internal documentation.
Control of materials needed to analyze and prepare a request for materials.
control, sampling, analysis and registering materials to the laboratory. BR> Provision of Confirmation or Failure to Approve the materials purchased for the laboratory.
Preparation of a work report for the superior official.
Introduction to quality control standards and requirements. Sufficient with GMP rules on quality control and other related units.
Ability to analyze the results of analysis.
Full acquaintance with English.

Possibility