Education

2015-2016 M.Pharm (Master’s) at University of Development Alternative

Result: cGPA-3.37 (Out of 4.00)
Duration: 1 Year

Subject Courses Taught on Master of Pharmacy (General):
Advanced Pharmaceuticals Analysis, Advanced Biopharmaceuticals and Pharmacokinetics, Advanced Pharmaceutical Technology, Advanced Medicinal Chemistry, Advanced Pharmacology and Clinical Pharmacy, Regulatory Affairs, Drug Use Management and Toxicology, Pharmaceutical Marketing and Sales.

2009-2013 B.Pharm (Hon’s) at Bangladesh University

Reasult: cGPA-3.68 (out of 4.00)
Duration: 4 years

Subject Courses Taught on Bachelor of Pharmacy (Honors):
Inorganic Pharmacy, Physical Pharmacy, Physiology, Pharmaceutical Microbiology, Computer Science, English Language, Organic Pharmacy, Pharmacognosy, Pharmacology, Pharmaceutics, Mathematics, Bio-molecular Pharmacy, Pharmaceutical Analysis and Quality Control, Statistics, Herbal Medicine, Bio-pharmaceutics, Pharmaceutical Engineering, Health Economics. Toxicology, Hospital Pharmacy, Medicinal Chemistry, Advanced Pharmaceutical Analysis, Pharmaceutical Technology, Pathology, Regulatory Affairs, Clinical Pharmacy, Pharmaceutical Marketing and Management, Cosmetology.

Dissertation:
Title: A study on adolescence & pregnant during anaemia in Dhaka City, Bangladesh
Supervisor: Zeb-Un-Nesa
Senior Lecture, Dept. of Pharmacy
Bangladesh University.

2005-2007 Alim (Science) at Tamirul Millat Kamil Madrasah

Result: GPA-4.67 (out of 5.00)
Duration: 2 years

1995-2005 Dakhil (Science) at Edrakpur K A Alim Madrasah

Result: GPA-4.67 (out of 5.00)
Duration: 10 years
NB:Golden A+ and board Scholarship

Experience

January'2019 to Present Senior Officer,Quality Control at Incepta Pharmaceuticals Ltd

Job Description:

1. Perform the laboratory analysis on organic and inorganic pharmaceutical formulations (tablet, capsule, liquid, and injections) doing wet chemistry test and instrumental test at the stage of in-process, finished products, packaging material and Raw materials operating HPLC, UPLC, UV, MASTERSIZER, ICP-OES, GC, LCMS, TOC Analyzer, AAS.
2. Use, calibration, trouble-shooting, function checking and maintenance for analytical instrumentation (pH meter, Conductivity meter, FTIR, Analytical Balance, KF Titrator.).
3. Inventory Management of laboratory Reagent, Laboratory equipment, Glass Apparatus, Chromatographic Column. WS, CRS (forecast, Requisition, purchasing, Sourcing, Issuing).
4. Water Analysis: Measuring pH, conductivity, heavy metal, nitrates TOC, residue on ignition, total solid, hardness (Calcium, Magnesium, Carbonate, and Bicarbonate), acidity & alkalinity, measurement of metals (Iron, Zinc, Manganese, Magnesium, Arsenic etc.) following batch/wet chemistry techniques and sampling techniques as per BP, USP, CP, EP.
5. Perform analytical methodology for water analysis, planning and executive water system validation (DQ, IQ, OQ, PQ).
6. Pharmaceutical Gas Analysis: Nitrogen Gas, Oxygen Gas etc. analysis according to wet chemistry techniques and sampling techniques as per BP, USP, CP, EP.
7. Coordinate a group of 7 (seven) members through strategic planning and decisions/discussions for target achievement orientations. Identify and monitoring the weaknesses of the fellow staff and help to overcome it and to build efficient and strong team for facing professional challenges.
8. Management of QMS related issues regarding Internal and external audit, deviation, out of specification (OOS), product complain, change control etc. with its Corrective and Preventive Action (CAPA) with non-conformity trend analysis.
9. Handling of retention sample of raw materials and finished products (receiving, register maintaining, shelfing, temperature and humidity monitoring of stability chamber etc.)
10. Review, draft and compilation of documents such as stability protocols, finished and raw material specifications, method of analysis, validation protocols and validation reports, transfer protocol, transfer report, SOP, Writing Standard Operating Procedures (SOP) and Standard Testing procedures (STP), Hold time study Protocol. Presentation for training in Laboratory.
11. Strictly monitor compliance of regulatory and GMP (Good Manufacturing Practice) standard practices in the quality control department following the Incepta Pharmaceuticals Ltd. Quality Policy and QC-GLP principles and guidelines.
12. Prepare plan for proper maintenance of QC instruments, utilities and reagents as per Good Laboratory practice (GLP).
13. Laboratory Waste Management (monitoring, collection, disposal and destruction, 5R technique) and laboratory housekeeping (5S)
14. Sampling & testing of raw and packaging material.
15. Analytical reports entry, raising requisition, issuing and releasing to the online production system, SAP.
16. Safety supervisor of QC laboratory (Hygienic, first aid, fire drilling earthquake, Management of PPE, safe operation of equipment).
17. Implement requirements of regulatory guidelines (Such as WHO, UKMHRA, USFDA, ISO, TGA, ICH and local) and update compliance of the requirements.
18. Organizing destruction of excess raw samples and finished product, Packaging Materials and expired document.
19. To prepare & coordinate training plans of the assigned person in QC laboratory for GMP and others.
20. Proper documentation and retention of Certificate of Reagent, laboratory equipment, Glass Apparatus, Chromatographic Column. WS, CRS.
21. Validation of test procedure as a validation team member.
22. Preparing Time Responsibility Plan (Gantt Chart) for personnel, equipment and as per requirement.
23. Attending all qualification activities for Life Cycle Management of all equipment such as DQ, IQ, OQ, PQ, MQ, CQ etc.
24. Maintain effective working relationship with the other department.
25. Assist to analyze market complain and find out the causes of complain and remedy with the help of production department.
26. Coordinate meeting with Quality Control, Product Development, Production, Engineering, Marketing and the Stakeholders.
27. Perform periodic gap analysis and ensure implementing of identified improvement on laboratory compliance.
28. Attending QC laboratory relocation and activities.
29. Coordination of user administration, system policy setting, data integrity and method/report management in Labsolution Data Manager Server.
30. Audit preparation and Audit facing experience of internal compliance (WHO, UKMHRA, UNICEF etc.) per assigned tasks

January'2015 to December'2018 Officer,Quality Control at Incepta Pharmaceuticals Ltd

Job Description:
1. Chemical & Physical analysis of finished product, Raw materials and packaging materials by using HPLC, UPLC, UV, MASTERSIZER, GC, LCMS, TOC Analyzer, AAS.
2. Daily function checking of pH meter, Conductivity meter, FTIR, Analytical Balance.
3. Reviewing analytical data for documentation.
4. Preparing CCF, DCCF.
5. Preparing Capex, User Requirement Specification (URS).
6. Perform minor type trouble shooting of different QC machinery.
7. Attending all qualification activities for Life Cycle Management of all equipment such as DQ, IQ, OQ, PQ, MQ, CQ etc.

July'2014 to December'2014 Management Trainee, Quality Control at Incepta Pharmaceuticals Ltd

Job Description:

1. Chemical & Physical analysis of finished product, Raw materials and packaging materials.
2. Reagent preparation, factorization, labeling and preserving
3. Record the real testing results doing the calculation. Finalize the document as soon test is over and keep the records up to date and hand over the in-process report to IPC staff.
4. Data entry, trending and reporting.
5. Disposal of laboratory waste following MSDS and GLP.
6. Perform laboratory house-keeping according to Good Laboratory Practice (GLP) standards and handling laboratory inventory stocks through monitoring usage following FIFO (first in first out).