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Khan M, Suleman
MSc Chemistry
Cell Number: 03453869347/03453880046
Position applied for Pharmaceutical industry Applied for Quality Control Job
Updated On April 24, 2016
PERSONAL INFORMATION
Name Khan Muhammad Father’s name Muhammad Suleman
Date of birth March 1, 1980 Marital status MARRIED
Age (Years) 35 years Nic # 45204-9370257-9
Religion Islam Nationality Pakistani
Currently Job in: PharmEvo Since 22-02-2009 still continued Job Designation; Sr. Executive Quality Control
Address Sachal Block D-42 (New No. 59/1) first floor near PCSIR Labs Main SUPARCO Road Karachi Sindh Pakistan.
Cell/Phone # +923453869347 & 923453880046 Email address khanmuhammad80@hotmail.com
Languages URDU ENGLISH, Skype address khanchemist121
ACADEMIC AND PROFESSIONAL Information
S
.
N
From
(Year)
To
(Year)
Educational and Professional
Certificates/Diplomas/
Degrees
Marks/Grade
Obtained
Percentage
Name of
School/Institute/
College/University
Course
Undertaken
Name of
Board/University
1 2001 2003
Msc Chemistry 71.40%
“A” Grade
Shah Abdul Latif
University
Oregano metallic
Chemistry,
Environmental
chemistry.
Shah Abdul Latif
University
2 1999 2001 Bsc Hons Side.
55.56%
“B” Grade
Shah Abdul Latif
University
General Chemistry
Organic Chemistry
Physical Chemistry
Physics.
Mathematics
Shah Abdul Latif
University
3 1995 1999 HSC
58.63%
“C” Grade
Govt. Degree College
Pir -Jo- Goth
Pre-Engineering BISE Sukkar
4 2001 2003 SSC
63.50%
“B” Grade
Govt. Single Section
HighSchool Ahmed pur
Science BISE Sukkar
Currently Working In Organization
Employer’s name Pharm EvoPvt Ltd.
Address Plot No. A-29, North Western Industrial Zone, Port Qasim, Karachi
Designation Sr, Executive Quality Control
Duration From February 21, 2009
Job description
ANALYTICAL INSTRUMENTS HANDLING
 HPLC LC 20 (Isocratic & Gradient)
 HPLC LC 20 (PDA Detector) Shimadzu
 HPLC LC 20 (Data Base ) (Shimadzu)
 UV Spectrophotometer (Shimadzu)
 GC Super 2010 (Shimadzu)
with HT3 Head Space ( USA)
 IR Spectrophotometer/FTIR/ATIR

2. 2
(Shimadzu )
 Dissolution Apparatus (Pharma Test)
 Disintegration Apparatus.
 Hardness Tester.
 Friability Tester.
 Conductivity Meter. (WTW Germany)
 pH Meter. (WTW Germany)
 Viscometer. (Brookfield)
 Karl Fischer. ( Mettler Toledo)
 Analytical Balance. ( Mettler Toledo)
 Potentiometer. ( Mettler Toledo)
 Color QA Instrument.
 Particulate Matter Counter
Job Descriptions in Different Section at Quality Operations in PharmEvo Pvt. Ltd.
Raw material Section Head.
Quality Control(Raw Material Section)
 Testing of Active and Excipients raw material & releasing of same after testing through SCM
 Perform Related Substance Performance, ‘’Impurities.
 Method development and Method Validation & Verification of raw material.
 Residual Solvent Testing,
 To maintain the instrument calibration record of daily, weekly, quarterly and yearly orderliness foundation.
 Implement the record of incoming Goods Receiving Note (GRN) of raw material and after releasing on Supply
Chain Management System “SCM”
 To insure the testing of raw material according to Standard Testing methods,
 Maintain the Inventory and testing record of incoming vender materials.
 Calibration of Primary Glassware and uphold the record of all crucial glassware.
 To insure standardization of Secondary working Standards against Primary working Standards.
 To providing Training to associates about instruments, SOP’s & testing methods.
 OOS Specification
Quality Control (Finish Product Section Head)
 Independently perform finish product testing according to follow GMP compliances.
 Method development and Method Validation & Verification Finish Products.
 Implement to maintain the record of incoming finish products.
 To insure the routine reports of finish products on Quality Management System (QMS)
 Testing planning on priority of urgency basis of finished products.
 Market Surveillance Studies, customer carp studies
 Maintain the inventory record of reagent, solvent stock and glassware.
 Arrange the regulatory data to regulatory department for MOH and International stakeholders.
Quality Control (Stability Study Section)
 Independently performs pre-stability/ GMP stability testing and all other analytical related activities including
new trial Batches (PD Product Development Trials batches.)
 Perform all laboratory work with proper planning and scheduling of jobs.
 Follow CGMPs GMPs, SOPs, HSE requirements and other applicable regulations.
 Review laboratory notebooks (routine testing).
 Execution of Pre-stability / GMP Stability samples and maintenance of laboratory database.
 Train associates on analytical methods and instrumentation case by case basis.
 Keep abreast on the latest changes in analytical science with limited supervision.
 Write / Review SOPs, qualification documents and protocols
 Participate in project teams and assist in troubleshoot and finding solutions.
 Conducts experiments, investigations, and special testing as needed for problem solving, to address regulatory

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issues, or to characterize drug substances/ drug products.
 Work closely with members of cross functional teams at different locations.
 Maintains GMP compliant, state-of-the-art analytical laboratories.
 Follow up ICH, WHO, FDA, DRAP Guidelines.
Quality Control (Packaging Study Section Head)
 Packaging material Testing.
 Proof reading of product leaf inserts & other packaging components to assure
Compliance with drug labeling & packaging guidelines.
 Maintain Records of Packaging Material.
 OOS Specification
 Releasing of All packaging Materials.
 Art work checking & approval after considering regulatory basics.
Professional Experience
S.N Name of Organizations Working Experience
1 Pharmevo Pvt Ltd. 22nd
February – 2009 Continued..…
2 ZUMARS Pharma Pvt.
11th
October 2008 up to 20th
February 20th
- 2009
(4.10 Months)
3 Epharm Laboratory Pvt Ltd. 26th
April 2007 up to 10th
October 10th
- 2008 ( 1.6 years )
4 Alina Combined pharmaceuticals Pvt Ltd. 19th
January 2007 to 26th
April 2007 (Three months six days)
5 TOTAL EXPERIENCE 9.Years 4 months professional experience of quality control department in different Pakistan base Pharmaceuticals.
Professional Trainings
S.N Trainings Venue
1 ISO 9001 : 2008 , ISO 14001 : 2004 Pharm Evo Pvt Ltd
2 OHSAS 18001 : 2007 Pharm Evo Pvt Ltd
3 Leadership Skills Pharm Evo Pvt Ltd
4 CGMP & GLP Practices National Productivity Organization “ NPO” House Defiance
5 Environment Health & Safety Pharm Evo Pvt Ltd
Computer Skills/Proficiency
S.N Skills
1 MS Office (Word, Power Point ,Excel, Outlook)
2 Kay Software for Quality Management System (QMS)
3 Supply Chain Management System (SCM)
4 LC Solutions
5 GC Solutions
6 Lab Solutions
7 Training on PIC/S and WHO standards (Internal Training)
8 WHO,PIC/S Project working body member in PharmeEvo Pvt. Ltd.