- 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
Qualifications
Bachelor's Degree in Chemistry, Industrial Chemistry, Analytical Chemistry, Biochemistry, or a related scientific field from a recognized institution.
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
