About this role
- Perform sampling, testing and analysis of in-process (IP) and finished products (FP) as per approved specifications and SOPs.
- Perform analytical testing using instruments such as HPLC, GC, UV, Dissolution Apparatus, FTIR and other laboratory equipment.
- Conduct physical and chemical testing of tablets, capsules and other oral solid dosage forms.
- Review analytical data, calculations, worksheets and laboratory records.
- Ensure proper documentation of analytical results in compliance with cGMP and GLP requirements.
- Prepare and maintain laboratory records, logbooks, SOPs and analytical reports.
- Handle OOS (Out of Specification), OOT (Out of Trend) and laboratory deviations in coordination with the reporting manager.
- Ensure calibration, qualification and preventive maintenance of laboratory instruments.
- Follow laboratory safety practices and maintain good housekeeping in the QC laboratory.
- Coordinate with Production and QA departments for sampling, testing and timely release of batches.