Company Introduction
Morepen Proprietary Drug Research is a pharmaceutical research organization engaged in active pharmaceutical ingredient development and analytical studies.
Core Responsibilities
- Prepare analytical study plans using laboratory notebooks, stability protocols, and method development records.
- Perform chromatographic trials on liquid chromatography and gas chromatography systems for active pharmaceutical ingredient samples.
- Review raw data printouts, chromatograms, and spectral files generated from analytical instruments.
- Compile method validation reports, stability summaries, and impurity profiling documents.
- Verify instrument calibration records and maintain laboratory logbooks and equipment usage registers.
- Store reference standards, reagents, and samples within controlled laboratory storage areas.
Skills and Technical Exposure
- High performance liquid chromatography systems with ultraviolet and refractive index detectors
- Gas chromatography and headspace gas chromatography equipment
- Analytical method validation techniques
- International Council for Harmonisation guideline documents
- Pharmaceutical development report documentation
Experience Context
- Work is carried out in an analytical research laboratory handling multiple active pharmaceutical ingredient projects.
- Daily tasks involve evaluation of stability samples, impurity studies, and method development trials.
- Laboratory output supports regulatory submissions and product development timelines.
- Without this role, analytical data generation and regulatory documentation would remain incomplete.
How to Apply
admin@morepenpdr.com
