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CURRICULUM VITAE
SANJEET KUMAR PANDEY
H. No. 782, Amravati enclave,
Behind Amravati School, Panchkula Pinjore road,
Distt: Panchkula (Haryana)
Contact No.: M: 08894317712, 09218552160
Email: Sanju1611@yahoo.co.in
QUALITY ASSURANCE/CONTROL / B.PHARMA WITH 10.0+ YEARS EXPERIENCE
Presently I am looking forward to work with your company. I am a hard working individual familiar with
strict reporting deadlines and in possession of good communication, interpersonal and supervisory skills I
have a workable knowledge of computer & MS-office. I would wish to move up the ladder of profession
and seek the challenge of working in a competitive environment.
EXPERIENCE
A) Presently working as Manager Q.A. with M/S Innova Captab Pvt Ltd, Jharmajri, Baddi. From
March 2010 to Till Date.
B) Worked as Quality Assurance Officer with M/S Ankur Drug & Pharma Ltd. Baddi H.P. from Dec.
2008 to March 2010.
C) Worked as Quality Assurance Officer with M/S Famy Care Ltd. Sarigam Valsad Gujrat from Feb.
2008 to Nov. 2008.
D) Worked as Quality Control Officer with M/S Innova Captab., Jharmajri, Baddi. From Oct. 2006 to
Jan. 2008
E) Worked as Q.C.Chemist with M/S Moraceae Lab (P) Ltd Lucknow (UP) from July 2005 to Sept.
2006
COMPANY PROFILEINNOVA CAPTAB PVT. LTD.
Innova Captab Pvt. Ltd. is an organization involved in formulation of Cephalosporin drugs with strength
of 200 employees. It is engaged in manufacturing pharmaceuticals products viz. Tablet, Capsule, Dry
syrup and Dry injection powder dosage form.
Site is WHO GMP, Kenya & TFDA approved.
Innova Captab Pvt. Ltd. is basically Loan Licence & Third Party company doing job work of following
groups i.e. Glenmark, Micro Lab, Cipla, Abbot, Alkem, Intas, Unichem, Lupin pharma, Macleods
Pharma, Ptheco Pharma, Khandelwal group etc.
COMPANY PROFILE ANKUR DRUG & PHARMA LTD.
An ISO, GMP & W.H.O. Certifiedcompany in Manakpura, Nalagarh, BADDI (H.P.) A good mfg of
Tablet, Cap, Dry syrup, suspensions/tonics. Contract manufacturing for CIPLA LTD, JUBILIANT,
DR.REDDY, RANBAXY LTD, TORRENT LTD, TRANSBIOTIC LTD, HINDUSTAN
ANTIBIOTICS LTD, SHREYA LIFE SCIECNES, KARNATAKA ANTIBIOTICS LTD,
NICHOLAS PIRAMAL, AJANTA PHARMA, ELDER PHARMA, SANDOZ etc.
COMPANY PROFILE FAMY CARE LTD.
Famy care ltd is world third largest manufacturer of Oral contraceptive pills and India largest
manufacturer.
Our products of Hormonal formulations are available in more than 40 countries worldwide. We are an
approved supplier of UNFPA, PSI, and Crown Agents-UK&PAHO. Our Products are supplied to projects
run by DKT, World Bank, IPPF and Ministry of Health in various parts of the world.
Site is USFDA, MHRA & MCC approved.

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COMPANY PROFILEINNOVA CAPTAB
Innova Captab. is an organization involved in formulation of drugs with strength of 150 employees. It
is engaged in manufacturing pharmaceuticals products viz. Tablets, Capsules, Ointment.
Innova basically Loan Licence company doing job work of following groups i.e. Lupin pharma, Macleods
Pharma, Ptheco Pharma, Khandelwal group etc.
COMPANY PROFILE MORACEAE LAB. (P) LTD.
Moraceae Lab. (P) Ltd. organization involved in formulation of tablets, liquid & ointment with strength
of 150 employees. Site is WHO-GMP, & ISO 9000 &2001 approved.
APPROVAL
I have approval in Quality control in Chemical, Instrumental and Microbiological section.
CURRENT JOB PROFILE
1) Process Validation, observation of all steps & preparation of their documents.
2) Equipment installation, preparation of IQ, PQ, OQ. Protocol
3) Handling of deviations, Change controls & non confirmation reports.
4) Work as a Team member to achieve the Target without compromising any Quality Parameter.
5) Participates in Cleaning Validation.
6) Execution of Calibration of Instruments.
7) Activity Participated in solving the issues and products related Problems with proper co-
ordination with the concern person.
8) Manpower allocation.
9) Conducting INTERNAL -AUDITS
10) Conducting VENDOR AUDITS. (RM &PM).
11) Water system Qualification and Validation
12) HVAC Qualification and Validation
13) Proper monitoring of whole section from vendor of raw / packing material to dispatch of finished
goods.
14) To keep Track Record of Calibration and Validation/schedule.
15) Warehouse Audit and periodic monitoring.
16) Technology transfer of new product at the site by coordination with R&D dept.
17) Proper monitoring of documents related to the production, Q.C, and Q.A department.
18) To maintain cGMP throughout production activities.
19) Proper planning to attain the market complaint and solve out the problem.
QUALITY CONTROL KNOWLEDGE
1. Ensure that S.O.P is available for each process and equipment.
2. Ensure that the SOPs are followed.
3. Maintain individual chemist notebooks on a daily basis.
4. Analyze the samples as per pharmacopoeia or in house methods without any
deviations.
5. Prepare the certificate of analysis for each sample analyzed and report the correct
values in the certificate of analysis.
6. Update and maintain the equipment log cards of each equipment immediately on use.
7. Ensure the chemicals, solutions and reagents are within their stipulated shelf life and
can be used for the test being performed.

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8. Ensure that the volumetric solutions are standardized and properly recorded.
9. Ensure that the volumetric solutions are re-standardized prior to use if the
restandardisation is due.
10. Ensure sampling of RM/PM/in process/finished goods is done strictly in accordance
to the S.O.P.
11. Ensure proper status labeling of all materials sampled, analyzed and released for
production or dispatch.
12. Ensure that all reports, records, documents are properly filed in an easily retrievable
manner.
13. Ensure that the GRN are forwarded to the respective departments once the testing and
report is completed.
14. Ensure that the samples sent to public testing laboratory are for valid reasons only and
maintain proper records of the samples sent.
SPECIFIC RESPONSIBILITIES.
In addition to all the functions listed under the category as General, the following
responsibilities shall be taken-
 To approve the specifications for all materials,
 To select and Train the staff for Quality control.
 To handle the QA related functions in absence of QA manager.
 To report Management on QC issues.
 Ensure proper discipline and adherence to GLP in QC.
AUTHORITY
 To release the raw and packaging materials for production.
 To release the in process bulk for packing.
 To release the finished product for distribution.
 To reject the raw materials/packing materials/in process samples/finished products.
 To review and revise documents.
 To order for spares/chemicals/service/equipment/outside calibration or service as
required.
INSTRUMENT HANDLLING
 HPLC (Auto sampler Shimadzu LC2010CHT, Manual also)
 UV SPECTROPHOTOMETER (Shimadzu 1700, 1800)
 POLARIMETER, KF TITRATOR
 DISSOLUTION APPARATUS
 pH METER, CONDUCTIVITY METER,
 REFRACTOMETER, LEAK TEST APPARATUS,
 MELTING POINT ETC.
AUDIT EXPOSURE
USFDA, GHANA, BANGLADESH, KENYA, SHRI LANKA& Other AFRICAN COUNTRY in Famy
Care Ltd, Sarigam
WHO & ISO in Ankur drugs & Pharma and Lead the audit of WHO GMP, Kenya & Tanzania at Innova
Captab Pvt. Ltd., Baddi.
WHO GMP, KENYA & TFDA in Innova Captab Pvt. Ltd, Baddi
EDUCATIONAL PROFILE
* B. Pharma from Technical University Lucknow (U.P) 2005
* 10+2 from U.P. Board Allahabad (U.P) 1995

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* 10th from U.P. Board Allahabad (U.P) 1993
TECHNICAL SKILL
Operating System- Window- XP. SAP,
Operating Marg, Euzen & SAP Software.
PERSONAL PROFILES
D.O.B. : 16-12-1978
Sex : Male
Marital Status : Married
Language Known : Hindi, English
Family Profile:
Father’s : Mr. Lal Mani Pandey (Lecturer)
Occupation : Teaching
Permanent Address : Vill. Beermau, Post: Pike Nagar
Distt. Pratapgarh (U.P.)
CURRENT CTC: 7.20 Lac/Annum
NOTICE PERIOD: Min. 1 MONTH
EXPECTED SALARY: NEGOTIABLE
Date:
Place: (Sanjeet Kumar Pandey)