- Develop and maintain calibration protocols for laboratory instruments like UV spectrometer, pH meter, thermometer etc.
- Perform stability studies on pharmaceutical products to ensure compliance with regulatory requirements.
- Conduct quality analysis of raw materials, intermediates, and finished products using various analytical techniques such as UV spectrophotometry, HPLC, GC, FTIR, ICP-MS etc.
- Collaborate with cross-functional teams to resolve issues related to product development and manufacturing.
- Ensure accurate documentation of test results, protocols, and reports according to cGMP guidelines.