Shadab is applying for a position in Quality Assurance with over 6 years of experience in QA documentation and process monitoring. He currently works as an Assistant Officer and documentation lead at Parabolic Drugs Ltd, where he has helped set up a new facility. Prior to this, he held QA roles at Surya Pharmaceuticals and IOL Chemicals & Pharmaceuticals. His responsibilities have included audit preparation, technology transfer, documentation control, and ensuring compliance with cGMP standards. He is proficient in documentation systems, process validation, and coordinating with other departments.

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Resume
Photo
Shadab
Phone: 07814336832 ,09027344731
E-mail: shadabmoazzam@yahoo.com
Sub :-Application for Quality Assurance department
Asst.Officer/Officer
Objective
A challenging and performance oriented position in Quality Assurance Dept. with
a reputed Pharmaceutical Organization.
Synopsis
Working in Pharmaceutical industry with 6.0 year of experience in field of Quality
Assurance documentation and in-process quality assurance activities at production
floor. Comprehensive problem solving abilities, good verbal and written
communication skills, willing to learn and team facilitator. Problem-solving skills;
demonstrable creativity in thinking and planning with a trained eye for
organization development and a passion for competitive ideas. Good command of
professional knowledge, language and basic computer network technologies I am
able to quickly adapt to the environment and actively participate in various
activities of the Organization.
Work History
IOL Chemicals & Pharmaceuticals (Trident complex) Dhaula Barnala (PB)
Worked as a Tr. Chemist Production from May 2005 to June 2007.
Surya pharmaceuticals ltd Plot No.-383 panchkula (Haryana)
Worked as Junior Executive – Quality Assurance (QA), June 2007 to April 2011.
Parabolic Drugs Ltd (IV) (New facility), Dera Bassi Punjab
Working as Asst. Officer cum Pilot Plant Documentation incharge since April
2011 to till date (Good Exposure of working in new facility).

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Key Performance Areas
 Knowledge of document distribution and data controlling.
 In Process Quality Assurance (IPQA) activities at the Production floor.
 Review of Batch Records.
 Technology Transfer from R&D to plant scale.
 Preparation of audit compliance report.
 Implementation of the cGMP practices in the facility.
 SOP Preparation.
 GMP and SOP compliance.
 Supporting to the Dept. colleagues in Audit facing and audit compliance.
 Internal Audit.
 Water system Qualification in New facility.
 HVAC Qualification in new facility.
 Equipment Qualification and Validation Protocol Preparation.
 Preparation and issuance of batch manufacturing records.
 Other QA documentation e.g. change control, Deviations, Documentation
distribution.
 Contract manufacturing at vendor site including technology transfer.
Coordination with other Departments
 Coordination with other departments like Production, Quality Control,
Material Management, R&D and Regulatory affairs etc. for compliance
of day to day requirements in the facility.

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Audit Faced
 US – FDA
 WHO GMP Audit
 Pfizer Audit
Educational Qualification
 Passed High School from UP Board with IInd Div. in 1996.
 Passed Intermediate from UP Board with IInd Div. in 1999.
 Passed Graduation from MJP Rohilkhand University Bareilly with IInd Div. in 2002.
 Passed Post Graduation from MJP Rohilkhand University Bareilly with IInd Div. in 2005.
Computer Skills
 Operational proficiency in MS Excel, MS word.
 Basic knowledge of computer.
 Internet surfing.
Personal Details
 Permanent Address : Village & Post Rajabpur Distt. J.P.Nagar (UP) 244236
 Date of Birth : 20-06-1982
 Marital Status : Married
 Languages known : Hindi, English
 Hobbies : Reading, playing indoor as well outdoor Games, TV etc.
Correspondence Address:-
 Mohalla Meera Mali Gali House no.1238 Derabassi Distt.
Mohali (PB)
Date: (Shadab)
Place: