• Perform Analysis of Chromium (Chromite)
• Iron
• Magnesium Oxide
• Silica Oxide, on wet Chemistry
• A complete knowledge about XRF ( X.Ray Fluorescence)
• Know how to make a LOT/ Shipment

●Execute quality control testing and advice for adjustment if necessary
● Ensure issue certificate of analysis for clients (finished good) when applicable
● Handling certificate of analysis of incoming raw materials
● Recipe adjustments of the products assessment in the central data base
● Prepare lab individual shift activity reports
● Evaluate all internal and external product evaluation requests and prepare test reports
● Reports and Documentation
● Ensure that Lab cleanliness and safety standards are maintained
● Develop and qualify new testing methods
● Train other analysts to perform laboratory procedures and assays
● Perform visual inspections of finished products
● Identify and troubleshoot equipment problems
● Evaluate new technologies and methods to make recommendations regarding their use
● Serve as technical liaisons between quality control and production.
● Write technical reports or documentations such as deviation reports, testing protocols, and trend analyses.
● Write or revise standard quality control operating procedures.
● Supply quality control data necessary for regulatory submissions.
● Receive and inspect raw materials.
● Prepare or review required method transfer documentation including technical transfer protocols or reports
● Sampling and testing of raw materials, intermediates and finished products using current pharmacopoeias, any associated ‘wet’ chemistry and instrumental techniques (HPLC, IR, UV), as appropriate.
● Preparing Quality reports, including analytical reports (for raw materials and finished products), Certificates of Analysis (CoA) (for finished products) and stability reports.
● Stability testing of products for new formulations and ongoing stability trials, using physical (pH, viscosity) and instrumental (HPLC, UV) techniques, as appropriate.
● Writing/reviewing Standard Operating Procedures (SOPs).
● Calibrating analytical equipment, as and when required.
● Observing and complying with company Health and Safety Policies.
● Observing and complying with company Standard Operating Procedures (SOPs).

●Execute quality control testing and advice for adjustment if necessary
● Ensure issue certificate of analysis for clients (finished good) when applicable
● Handling certificate of analysis of incoming raw materials
● Recipe adjustments of the products assessment in the central data base
● Prepare lab individual shift activity reports
● Evaluate all internal and external product evaluation requests and prepare test reports
● Reports and Documentation