Tamzid Zaman

• Planning, organize & execute the quality control tests for the incoming raw materials, finished products for tablets, capsules, liquids, suspensions, Sterile dry powder for vial injection & animal health products • Perform and lead investigations for Laboratory incidence and other cGMP violation of analytical work • Planning and monitoring the analytical method validation, cleaning validation & manufacturing process validation • Performing gap analysis of existing specification and method vs USP,BP & ICH guidance and update via change control • Preparation of SOPs (standard operating procedure) for Quality Control/ Quality Assurance activities and equipment's • Implementation of commercial real time stability & shelf life extension • Approving or rejecting starting material, packaging materials, intermediates, bulk and finished products • Perform Supplier Approval audit as a Qualified Auditor • Conduct Internal Quality Audit as a member of Internal Quality Audit Team • Manage Out Of Specification (OOS), Out of trend (OOT), Change controls, complaints, deviations, Investigation & Risk Assessment • Preparation of Corrective and Preventive Action (CAPA) of different audit observation • Ensure readiness and perfect technical status of the QC equipment, Reference/working standard & Reagents. • Analyzing QC activity monthly, prepare a productivity report. • Guide and train members of the QC team towards excellent work performance.

• Planning, organize & execute the quality control tests for the incoming raw materials, finished products for tablets, capsules, liquids, suspensions, Sterile dry powder for vial injection & animal health products. • Manage Out Of Specification (OOS), Out of trend (OOT), Change controls, complaints, deviations, Investigation & Risk Assessment. • Analyzing QC activity monthly, prepare a productivity report. • Manage analytical method development and validation. • Purchasing of new equipment for laboratory. • Carried out internal and external audits. • Monitoring the cleaning validation & manufacturing process validation.

• Performing analytical method development and validation. • Manage Out Of Specification (OOS), Out of Trend (OOT), Change control and deviation. • Updating and preparation QC related documents i.e. Specification, control directions. • Preparation of SOPs (standard operating procedure) for Quality Control/ Quality Assurance activities and equipment's.

Responsible for pharmaceutical finished product release testing, raw material testing and stability testing. Periodic review of SOP's and document reviews. I have also conducted method development and validation.

Responsible for calibration, maintenance and troubleshooting of laboratory instruments. Conducting OOS investigations. Following pharmacopoeia methods for testing pharmaceutical raw materials and finished products. Making up of laboratory reagents.

One month long in-plant training.

- Conduct tutorial sessions for students needing extra help out of class. - Assist Faculty Members in their research work. - Assist Faculty Members in preparing lecture notes. - Grade true-false, MCQs and other non-judgmental questions.