Jesmin Nahar

QA Associate Scientist

Talent

Laurelton, NYMember since July 29, 2026

QA InspectorHPLCIRUVPCATOMIC AbsorptionKarl FischerDissolution ApparatusFriability Test ApparatusQuality ControlGood Manufacturing PracticesISO guidelinesValidationChromeleon

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QA InspectorHPLCIRUVPCATOMIC Absorption

About

In the immediate position, I would prefer a dynamic and challenging job that utilizes my merit as well as experiences for the interest of the company and my career. In the long term, I desire to become an expert in QA/QC Chemist and to provide solution in critical situation.

Experience

QA Associate Scientist - Evaric Pharmaceuticals, Inc. - 155 Commerce Drive, Happauge, NY 11788

(2022-07)

All types of components/materials are sampled, inspected, and tested (where applicable) for the purpose of determining compliance with established specifications.

Monitor and ensure all phases of drug packaging comply with established specifications
Receive, inspect, release, and control labels and Outsets
Ensure quality compliance before, during, and after each packaging run
Review all requirements from QA scientist and engineering records (temperature and humidity data calibration and PM records)
Review online batch records in terms of completeness of signatures, entries, and actual reconciliation/yields before initiation of next processing step
Verify functionality of all equipment and associated controls during the batch run
Inspect packaging line during packing operation

QA Inspector II - Amneal Pharmaceuticals of NY, LLC - 50 Horseblock Road, Brookhaven, New York 11719

(2016-09 - 2022-07)

Quality Control Manager - Hallmark Pharmaceuticals Ltd. - B-63, BSCIC VA, Tongi Gazipur, Bangladesh

(2012-05 - 2013-09)

Implementation of Company Quality policy and ensuring compliance with quality standards.

Approve or reject starting materials, packaging materials, and intermediate, bulk, finished products and per-purchase raw material
Prepare and update all documentation related with testing, sampling instructions, specifications, test methods and validation
Ensure that the appropriate validations, including those of analytical procedures and calibrations of control equipment and process validation are done
Ensure that all necessary tests are carried out as mentioned in Product Master File
Check the maintenance of the QA/QC equipment and sanitation
Ensure WHO cGMP and ISO guidelines are followed
Coordinate with Commercial Department for vendor selection
Coordinate with Product Management and Regulatory Affairs for preparing of technical data, annexure and other document for Drug Administration
Ensure that all documents and records are preserved correctly
Monitor and control environment of plant area
Directly monitor and control all the in-process tests/checks and instruct production for corrective measures if required
Arrange adequate stocks of reagents, glassware and consumables are available
Ensure that the required initial and continuing training of quality assurance personnel is carried out and adapted accordingly to need

Quality Control In-charge - NAVANA Health Care Limited - Rupshi, Rupgonj, Narayangonj, Bangladesh

(2008-07 - 2012-05)

Management of quality control operations and pharmaceutical testing procedures.

Approve or reject starting materials, packaging materials, and intermediate, bulk, finished products and pre-purchase raw material
Prepare and update all documentation related with testing, sampling instructions, specifications, test methods and validation
Ensure that the appropriate validations, including those of analytical procedures and calibrations of control equipment and process validation are done
Ensure that all necessary tests are carried out as mentioned in Product Master File
Check the maintenance of the QA equipment and sanitation
Ensure WHO cGMP and ISO guidelines are followed
Coordinate with Commercial Department for vendor selection
Coordinate with Product Management and Regulatory Affairs for preparing of technical data, annexure and other document for Drug Administration
Ensure that all documents and records are preserved correctly
Monitor and control environment of plant area
Directly monitor and control all the in-process tests/checks and instruct production for corrective measures if required
Arrange adequate stocks of reagents, glass wares and consumables are available
Ensure that the required initial and continuing training of quality assurance personnel is carried out and adapted accordingly to need
Determine complex chemical conversions including Radio-isotopic characteristics in medicines conducting programs of data collection and analysis to identify and quantify toxic-ants
Develop and conduct new methods of analysis to ensure quality of materials

Senior Quality Control Officer - AVANA Pharmaceuticals Limited - Rupshi, Rupgonj, Narayanganj, Bangladesh

(2007-07 - 2008-06)

Quality Control Officer - AVANA Pharmaceuticals Limited - Rupshi, Rupgonj, Narayanganj, Bangladesh

(2003-12 - 2007-07)

Assistant Control Officer - AVANA Pharmaceuticals Limited - Rupshi, Rupgonj, Narayanganj, Bangladesh

(2001-04 - 2003-12)

Perform analysis testing and quality control operations in pharmaceutical manufacturing.

Perform analysis testing of raw materials, bulk materials, and intermediates product
Operate a variety of instruments in the QA Laboratory such as HPLC, IR, UVPC, ATOMIC Absorption, Karl Fischer, Dissolution Apparatus, and Friability Test Apparatus, etc.
Document preparation and report writing
Prepare reagents and proper labeling; conduct various validation works
Conduct routine microbiological tests
Perform and monitor calibration of QA equipment
Direct Quality control procedures and manage the chemical technicians and technologists
Develop and conduct new methods of analysis to ensure quality of materials
Process and devise new technical applications of chemicals and compounds
Determine complex chemical conversions, including Radio-isotopic characteristics in medicines, conducting programs of data collection and analysis to identify and quantify toxicants