presently working in F&D and DPI Projects

Production and Quality,and formulation and development

Mentored of four Formulation Scientists o Successful development of oral and liquid and semisolid formulations o Handled and formulated oral liquid products for controlled Conducted studies related to preformulation and formulation of drug products, including dissolution, and additional studies as related to the stability, delivery of product.Worked in collaboration with Manufacturing to transfer technology and manufacturing processes from R&D to Manufacturing site.Prepared submission batches as per FDA requirements.Wrote master formulas, manufacturing procedures, product development reports, validation reports, and standard operating procedures.Involved in technology transfer of products from external manufacturers o Develop and validate analytical methods as per FDA regulatory requirements.• Reviewed raw data and production trend forecasts to effectively plan operations.

•Maintaining online BMR and BPR along with its retrieval.• Maintaining Log Books• Maintenance of temperature, humidity and pressure conditions in critical areas.• Maintain cleanness and standard for Line clearance required as GMP.• Excellent man power handling.• Responsible for in process checking.• Maintained clean and well-organized production areas to avoid violations or unnecessary work delays due to hazards or inefficient layouts.• Established operational objectives and work plans and delegated assignments to subordinate managers.• Implemented policies and standard operating procedures for continuous improvement.• Prepared, calibrated and monitored production machinery to maintain optimal production levels and consistently achieve daily targets.• Monitored daily and weekly key performance indicators to maintain on-track status.

Maintaining online BMR and BPR along with its retrieval.• Maintaining Log Books• Maintenance of temperature, humidity and pressure conditions in critical areas.• Maintain cleanness and standard for Line clearance required as GMP.• Excellent man power handling.• Responsible for in process checking.• Maintained clean and well-organized production areas to avoid violations or unnecessary work delays due to hazards or inefficient layouts.• Established operational objectives and work plans and delegated assignments to subordinate managers.• Implemented policies and standard operating procedures for continuous improvement.• Prepared, calibrated and monitored production machinery to maintain optimal production levels and consistently achieve daily targets.• Monitored daily and weekly key performance indicators to maintain on-track status.

T. Chemist at Analytical Dept.