QUALITY CONTROL ANALYST / CHEMIST
Job summary
To support the production of safe, effective, and high-quality pharmaceutical products by conducting laboratory testing, analyzing results, and ensuring compliance with quality and regulatory standards. The role contributes to KPI's commitment to good health through accurate, timely, and reliable quality control activities.
Job descriptions & requirements
- 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
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Understanding of pharmacopoeia standards (USP, BP, EP, etc.)
Laboratory documentation and record-keeping
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Data analysis and interpretation of test results
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Calibration and operation of laboratory equipment
Investigation of Out-of-Specification (OOS) and Out-of-Trend (OOT) results
Additional training or certification in Quality Control, Good Manufacturing Practices (GMP), or Good Laboratory Practices (GLP) is an added advantage.
How to Apply:
All applications will be received and reviewed through the BrighterMonday Portal by clicking on the 'Apply Here' section
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