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Curriculum Vitae
TANVEERAHMED
Contact Number: 01711279191 & Home: 01727209465
Contact Address: House: 253/4, Sultangonj Road, Royer Bazar. Dhaka-1209
Bangladesh
e-mail: tanveer.russel@gmail.com
Specialization:
Having work experiences more than10 years in Quality Assurance, Validation & Quality control laboratory. I
have participated in some international regulatory inspections (i.e. TGA Australia, GCC, ANVISA Brazil,
Austrian Agency for Health and Food Safety and ISO 9001 & ISO 13485 & CE certification audit by UL LLC,
USA) during this period.
I also worked with Lachman Foundation, USA (FDA Consultant) during my job in QA Department of Incepta
Pharmaceuticals Limited (New facility built in Dhamrai for US-FDA Market).
Reg. no. of Pharmacy Council of Bangladesh: A-2889
CAREER SUMMARY
Name of Company
Current/ Last
Position
Department / Area Duration
Julphar Bangladesh Ltd.
Head of QA (Deputy
Manager, QA)
Quality Assurance 15/05/2016 to 17/08/2016
Ispahani Alliance
Pharmaceuticals Limited
Quality Assurance
Manager
Quality Assurance 07/12/2014 to 31/03/2016
Incepta Pharmaceuticals
Ltd
QA In-charge (PDF
Facility, Dhamrai Unit)
Quality Assurance
(Dhamrai Unit)
06/07/ 2011 to 30/11/2015
Beximco Pharmaceuticals
Ltd.
Assistant Manager,
QA
QA Department (Track-II) 15/03/2006 to 25/06/2011
DETAILS OF CAREER
15/05/2016 to 17/08/2016: Quality Assurance of Julphar Bangladesh Ltd.
 Maintain and ensure the quality assurance and quality control at the site that the products released are fit
for their intended use; comply with the requirements of regulatory requirements and has authority for the
site decisions affecting product quality and sustainable cGMP compliance and leads the site's Quality
initiatives.
 Implementing Quality Management System and accountable for overall Quality and regulatory compliance
at the site, resulting in a reliable product supply to customers through the company’s Supply Chain.
 Oversee the assignment and completion of investigations, corrective/preventive actions and escalating
risks to Corporate Leadership with a plan of action, mitigation and execution timelines.
 Manage Site QA QPIs/metrics, monthly reporting and corrective actions at the site. Analyze internal and
external Quality data and initiate effective preventive and corrective actions to reduce and eliminate
adverse trends.
 Ensure the established a comprehensive system with trained individuals managing the quality support
system and quality standards.
7/12/2014 to 31/03/2016: Quality Assurance Department of Ispahani Alliance Pharmaceuticals Ltd,
Dhaka. Bangladesh
 Develop, implement, manage, audit and maintain quality systems to support commercial and
development activities.
 Coordinate and perform all vendor qualification and compliance audits.
 Develop, manage and maintain document control system.
 Oversee investigations of all non-conformances (complaints, deviations, OOS).

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 Ensure that cGMP requirements and quality standards are recognized, understood and maintained
across the Company.
 Ensure in-process and finished products and processes conform to in-house policies and procedures as
well as other applicable regulations and guidelines.
 Work across all disciplines (e.g. manufacturing, quality control, engineering, technical service,
warehouse etc.) to ensure that the Company maintains a state of readiness for inspection by regulatory
agencies.
 Keep abreast of changes to quality regulations and guidelines, advising the top management team of
any business implications of these changes.
 Lead, manage and ensure proper training to any relevant CGMP topic throughout the company.
 Represent QA at senior management, project, Board, and review meetings.
6/07/2011 to 30/11/2014: Quality Assurance Department (Dhamrai Unit) of Incepta Pharmaceuticals Ltd,
Dhaka. Bangladesh
I was also doing my job at QA Department of Incepta Bioscience (New facility built for US-FDA Market) during
this period. I worked under the supervision of Lachman Foundation, USA. (01 January 2014 to 22 July2015).
Job Done in QA Department of Dhamrai Unit:
 Develop and maintain quality management system documentation, training program and document
control system including documents specific to regulatory and compliance processes and procedures.
 Conduct internal audits.
 Review and approval of documentation such as Site Master Plan, Validation Master Plan, Change
Controls, Deviations, OOS, CAPA, Market Complaints, Investigation Reports, Annual Product Review,
Specifications, Test Methods, BMR, BPR, SOPs, Training Documents, Process Validations, Cleaning
Validations and equipment/utility system qualification procedures & records and other regulatory affairs
documents.
 Release of finished goods.
24/09/2008 to 27/06/2011: QA Department of (Track-II); Beximco Pharmaceuticals Ltd., Tongi, Gazipur,
Bangladesh
Job Done:
 Overall monitoring of validation and qualification activities.
 Preparation, review and update of Site Master Plan and Validation Master Plan and SOPs etc.
 Facility Qualification, Process validation, cleaning validation, Analytical Method Validation, finished
products transportation system validation and their documentation (protocols and reports).
 Performance Qualification of manufacturing and packaging equipments/ instruments.
 In-process control activities.
 Preparation and updating of CTD Documents (Technical Part of Dossier) & other regulatory affairs
documents and delivery them to International Marketing Department.
15/03/2006 to 23/09/2008: Quality Control Department (Track-II) of Beximco Pharmaceuticals Ltd.,
Tongi, Gazipur, Bangladesh
Job Done:
 Analytical method validation activities.
 Stability testing of new doses form and ongoing stability.
 Stability study as per stability indicating validated methods.
 Analysis of in-process products and finished products.
 Operation, calibration and perform equipment qualification of laboratory equipments.
 To ensure relevant GLP and maintain safety at work in the laboratory.
 Documentation: Preparation of Analytical method validation protocol & reports, Stability study protocol &
reports, Equipment Qualification Documents, SOPs, STPs and other documentation meeting cGMP and
regulatory requirements.
 QC Equipments/Machines: HPLC (Waters & Shimadzu), Atomic Absorption Spectrophotometer
(Shimadzu), TOC Analyzer (Shimadzu), FTIR-Spectrophotometer (Shimadzu), Dissolution Machine,
Disintegration Machine, Friability Tester, Tablet Hardness Tester, pH Meter, Weighing Balances, HPLC
Water Purification System, Vacuum Oven, Stability Chamber

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EDUCATION QUALIFICATION
Name of
Exam
Group /
Subject
Exam Year Board Institution Result
B. Pharm. Pharmacy 2003 (Exam. Held in 2005) - University of Dhaka 2nd Class
H.S.C. Science 1998 Dhaka Dhaka College 1st Division
S.S.C Science 1996 Dhaka
Government Laboratory
High School
1st Division
TRAINING
Title Organization / Trainer Place Year
Quality Management Workshop
on Depot Medroxy Progesterone
Concept Foundation Thailand 2012
EU GMP guideline incl. annexes Dr. Ursula Koller, GMP Auditor &
Consultant
Bangladesh 2010
Cleaning Validation Asia Pacific Consultant Pty Ltd. Australia
(Trainer: Wayne Mc Kenzie)
Bangladesh 2009
Sterile facility operation Asia Pacific Consultant Pty Ltd. Australia
(Trainer: Wayne Mc Kenzie)
Bangladesh 2008
In-plant Training Organon (Bangladesh) Limited Bangladesh 2006
ACADEMIC ACHIEVEMENTS: Primary Scholarship in 1990 & Junior Scholarship in 1993.
COMPUTER LITERACY: MS Word, MS Excel, MS Power Point, e-mail and Internet operations.
LANGUAGE COMPETENCY: Both well in English and Bengali.
EXTRA CURRICULAR ACTIVITIES: Had taken part in Bata School Hockey Tournament 1995.
PERSONAL DETAILS
Name : Tanveer Ahmed
Father : Aziz Ahmed
Mother : Samsunnahar
Address : 253/4, Sultangonj Road, Royer Bazar, Dhaka-1209. Bangladesh
Home District : Chandpur
Contact Number : 01711279191; Home: 01727209465
Birth Date : March 17, 1981
Marital Status : Married
Nationality : Bangladeshi
NID : 2692848060485
______________________
(Signature)