RAMYA KODURU

1)Analysing drug findings in the and medicine reactions on both clinical and pre-clinical studies.

2)performing multiple extractions for seperating medicines and drug using blood,plasma and urine samples as medium fot both clinical and pre-clinical studies.

3)Operated and maintained LC-MS/MS instruments (Sciex Triple Quad, Waters UPLC) for measuring small compounds in biological matrices.

4)Used tested techniques to analyse and interpret raw data, making sure that SOPs, FDA/EMA bioanalytical criteria, and project schedules were followed.
5)usage of LIMS and ELNs to maintain thorough laboratory documentation; in order to maintain quality standards, data discrepancies were identified and looked into.

• Acts as a Cleaning Validation analyst for determining free contamination of Equipment’s which are used under the Manufacturing Sectors for processing different types of medicines.
• Testing samples like Swabs, Needles, Orifices and tested for validating carbon content with TOC,microbca,nitrates,conductivity instruments. Validating them by several quality checks.
• Developed and validated analytical methods for detection of cleaning residues, ensuring compliance with FDA and cGMP regulatory standards.
• Collaborated with QA, manufacturing, and validation teams to troubleshoot and resolve cleaning failures or deviations.
• Purity assessment for the water samples which are used for the cleaning in the Equipment.

• Validating and documentation of the samples for the quality testimony. Preparation and filtering of the samples are concluded.
• Recognition of raw materials and physical appearance-ensuring materials quality by API and examining pigmentations of the raw materials.
• Testing and measurements: absence of microbial contamination is a key mark. -performance of analytical techniques by HPLC.PH level by 7 for stability and effectiveness of the sample.
• Rheological and stability testing: ointment consistency in storage locations and ensuring product throughout its shelf life.
• Documenting the samples: Managing testing records by batch id and making GMP (good manufacturing practices).
• Product release: Qualified product passes the test case and releases in the market.

Additional Responsibilities:

• Preparation of the buffers in bulks for vaccine production (covid era)