 Evaluation & testing of finished drug product. Evaluation & testing of raw materials. Data interpretation and presentation of results. Stability studies and trend analysis for Pharmaceutical drug products.  Dissolution Profiling and comparative study of registration sample with established products.  Drug adultration testing for Health supplements and herbal medicine.  Calibration and maintenance of Q.C.instruments.  Perform Process Validation, Method Validation, and Method Transfer.  Maintain quality system according local SOP, GMP, and ISO 17025 requirements.  Resolve quality related deviations by performing Out-of-Specification investigation (OOS), Out- of-Trend Investigation (OOT) and Corrective & Preventive Actions (CAPA) in the timely manner. Team leader, involved in conducting induction for newly-hired staff. Work planning & coordination with upper management. Assistance, guidance & coaching of junior staff. Rectifying issues encountered by team members through troubleshooting.

 Determine quality objectives, participate in development of quality strategy and quality directions. To assure consistency validating new products. Developing and enforcing processes by providing documentation & leading and coaching QA & QC junior colleagues.  Ensure & maintain QC equipment in good conditions by performing routine checks. Maintains and improves our product quality by system, compliance and surveillance audits. Prepares documentation and reports by collecting, analyzing and summarizing information and trends including failed processes, stability studies, recalls, corrective actions, and re-validations.  To assure ongoing compliance with quality and industry regulatory requirements.

 Work closely with others in a team environment within the Quality Control laboratory and act as an integral team member on multidisciplinary teams that provide support for Manufacturing and Product Development activities. Complete activities in compliance to applicable company procedures, specifications, and compendia requirements in an efficient and high quality manner. Perform testing, analysis and data reporting for test samples.  Execute analytical methods for testing on a variety of test samples including raw material, in-process/fmished product, stability, validation , Process Development and R&D test samples. Prepare and standardize laboratory reagents and test solutions. Document work with particular attention to detail and in compliance with Good Documentation Procedures. Generate Data Reports and Forms . Operate, calibrate, perform preventative maintenance and when required trouble shoot and repair minor problems with Analytical Instrumentation. Support and execute activities for test method validation and transfer. Participate in test method development. Author, edit, and review technical reports, protocols, specifications and SOPs. Continually review programs and systems to develop and drive improvements in efficiency, effectiveness and quality. Participate in and/or lead independent and team based investigations. Determine root causes for Out of Specification and Atypical test results. Develop, propose and monitor corrective actions. Perform all work according to applicable safety procedures using good laboratory techniques and using safe operation of laboratory equipment.

Testing all Finished product(Tablet,Capsule,liquid and suspension)Handling OOS and OOT.Handling Q.C.Instruments like HPLC,AAS,DISSOLUTION,UV,FTIR,POLARIMETER and other basic instruments.

Testing all stability product,Compiling Trend with previous interval.Anual Product review.Handling OOS and OOT.Handling Q.C.Instruments like HPLC,DISSOLUTION,UV,FTIR,POLARIMETER and other basic instruments.Packline inspection,Lineclearance for Manufacturing ang Packing area.