1. Coordinate and perform quality control tests on raw materials, in-process and finished products to verify their compliance with specifications and standards.2. Maintain accurate records of quality control tests, results, and investigations. Ensure that all documentation is complete, organized, and easily accessible for audits and inspections.3. Assist in investigating deviations, out-of-specification results, and other quality-related issues.4. Provide training to quality control personnel on testing procedures, equipment operation, and quality standards. Ensure that staff members are competent and capable of performing their assigned tasks effectively.5. Oversee the calibration, maintenance, and qualification of laboratory equipment and instrumentation used in quality control testing.6. Review and approve quality control documents, including test methods, specifications, protocols, and reports.7. Participate in internal Audits.8. Ensure that all quality control activities are conducted in compliance with safety protocols and procedures.

1. Perform wet and instrumental analysis (HPLC, UV, Melting point device, Viscometer, Conductivity meter, pH meter, Balance, ovens, Polarimeter device, Centrifuge, Sieve analyzer and Disintegration tester) of raw materials.2. Perform physical testing and chemical analysis of pharmaceutical material.3. Sampling of raw material according to approved SOPs.4. Prepare and standardizes working standards, volumetric solutions, reagents and indicators.5. Follows the approved controlled standard operating procedures, raw materials and packaging.6. Perform QC testing on in-process and finish products to make sure product specifications were met.7. Prepare Standard operating procedures for analytical testing of raw materials and finish products.8. Preparation of Protocol, Reports Sample Placing data record and Stability Chamber maintenance.9. To ensure that the stability studies (Export Products and Local Products) are carried out as per schedule.10. Testing of stability products according to the schedule and protocol requirements.11. Analysis of results and finalized the report of stability products.12. Incineration of the Stability Products.

1. Preparation for Process validation protocol and report after testing of all the samples.2. To performed comparative dissolution profiling.3. To performed Analytical method validation and verification.4. To perform Force degradation study for pharmaceutical products.5. Development of analytical method for non-pharmaceutical products6. Planning and executing of Process validation activities and the creation of validation documentation.7. Recording, analyzing and distributing statistical information.8. Preparing Master Validation Plan.9. Handling queries and removing Non Conformances of audit.

1. Preparation for Process validation protocol and report after testing of all the samples.2. To performed comparative dissolution profiling.3. To performed Analytical method validation and verification.4. To perform Force degradation study for pharmaceutical products.5. Development of analytical method for non-pharmaceutical products6. Planning and executing of Process validation activities and the creation of validation documentation.7. Recording, analyzing and distributing statistical information.8. Preparing Master Validation Plan.9. Handling queries and removing Non Conformances of audit.

1. Perform wet and instrumental analysis (HPLC, UV, Melting point device, Viscometer, Conductivity meter, pH meter, Balance, ovens, Polarimeter device, Centrifuge, Sieve analyzer and Disintegration tester) of raw materials.2. Perform physical testing and chemical analysis of pharmaceutical material.3. Sampling of raw material according to approved SOPs.4. Prepare and standardizes working standards, volumetric solutions, reagents and indicators.5. Follows the approved controlled standard operating procedures, raw materials and packaging.6. Perform QC testing on in-process and finish products to make sure product specifications were met.7. Prepare Standard operating procedures for analytical testing of raw materials and finish products.8. Preparation of Protocol, Reports Sample Placing data record and Stability Chamber maintenance.9. To ensure that the stability studies (Export Products and Local Products) are carried out as per schedule.10. Testing of stability products according to the schedule and protocol requirements.11. Analysis of results and finalized the report of stability products.12. Incineration of the Stability Products.