• Knowledge of Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP)

• Inspections, Sampling & testing of all raw materials, packaging materials, in-process materials, and finished products.
•  Inspection, sampling, and testing of demineralized water used in the manufacturing of products.
• Approving or rejecting materials and finished products depending on their status to comply with the set quality specifications.
• Doing the calibration of test equipment and validation of analytical methods and procedures to ensure that the analytical results obtained are both precise and accurate.
• Inspecting all quality control laboratory areas to ensure that they comply with Good Laboratory Practices (GLP) in all aspects of construction, use, and maintenance.
• Proficiency in analytical testing techniques (e.g., HPLC, UV Spectrophotometry, FTIR, Dissolution Testing, Titration)
• Sampling and testing of raw materials, packaging materials, in-process, and finished products

• Understanding of pharmacopoeia standards (USP, BP, EP, etc.)

  Laboratory documentation and record-keeping

• Data analysis and interpretation of test results

• Calibration and operation of laboratory equipment

  Investigation of Out-of-Specification (OOS) and Out-of-Trend (OOT) results

How to Apply:

All applications will be received and reviewed through the BrighterMonday Portal by clicking on the 'Apply Here' section