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COVER LETTER

DEAR SIR/MAM ,

I AM AWARE OF A JOB OPENING AT YOUR COMPANY


AND I AM VERY EXCITED ABOUT IT. MY BACKGROUND IN
PHARMA SHOULD BE AN EXCELLENT FIT WITH THE JOB
SPECIFICATIONS.

I AM EXPERIENCED PERSON, I AM ALSO AN EXCELLENT


COMMUNICATOR, A QUICK LEARNER, AND HAVE WELL
HONED ADMINISTRATIVE SKILLS. I BELIEVE I AM AN
EXCELLENT CANDIDATE FOR A JOB WITH YOUR FIRM.

THANK YOU SO MUCH FOR YOUR CONSIDERATION AND


HOPE THAT WE WILL HAVE A CHANCE TO MEET SOON.

SINCERELY

BANSHI DHAR GUPTA

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RESUME
BANSHI DHAR GUPTA

S/O SHRI MISHRI PRASAD GUPTA


A.S. HOUSE ZAMANIA (R.S)
DISTRICT-GHAZIPUR (U.P)
MOBILE No- 7076202525
Email-id:-g.banshi@yahoo.com
CAREER OBJECTIVE To work in a challenging job environment that utilizes my skill and abilities

and offers ample learning opportunities.


EDUCATION  B.Pharm
QUALIFICATION

TOTAL
EXPERIENCE
 7.2 Years

WORK  AKUM DRUG PHARMACEUTICAL LIMITED


EXPERIENCE
Designation : Worked as QA Trainee and as a Q.A Officer
Work Period : SINCE JUNE 2012 TO JULY 2015
 SUN PHARMA LABORATORIES LIMITED
Designation : Worked as Senior Officer QA and Working as a Q.A
Executive

Work Period : Since AUGUST 2015 TO TILL NOW


JOB DESCRIPTION  Review Executed BMR (Batch Manufacturing Records) and BPR (Batch
Packing Records) .
 Review Master BMR and BPR to verify the process, procedure,
instruction, in process parameter as per Master Product Specification.
 Lead as a representative for Product Technology Transfer as a Q.A
prospective.
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 Handle clinical trial study product manufactured at site for filling of
product.
 Handle DCGI registration product manufactured at site for commercial
approval.
 Evaluate and review all documents which are required for clinical trial
study and DCGI registration of product before submitting to IRA Team for
product registration.
 Provide justification whenever required by regulators regarding any query
related products registration.
 Play a lead role with my team in validation and qualification of product
process, equipments, utility, and facility.
 Prepare, Design, Review Protocol and generate report accordingly
established the process and parameters in Standard Batch Record.
Product process qualification of solid dosage form.
Cleaning validation and verification.
Hold time study of Product at different stages of process.
Hold time study of clean equipment.
Transport validation for product.
Qualification of manufacturing and packing process equipments.
Qualification of HVAC System.
Qualification of water system.
Qualification of compressed air.
Qualification of facility.
Temperature mapping of controlled area.
 Do risk assessment when ever required for risk evaluation regarding
product process and qualification.
 Responsible for Handling of Change Control, Deviation, CAPA and other
QMS Documents through Track Wise Application System.
 Responsible for Preparation of Site Master File, Validation Master File,
Cleaning Validation Master File, Equipment Qualification Master File.
 Review of Layouts/Drawings of Plant like System Zoning Layout,
Pressure Zoning Layout, Man and Material Movement Layout after any
renovation which may impact Site Master File.
 Responsible for preparing and reviewing of SOPs which are concern with
my Job responsibility and schedule revision through EDMS Application.
 Provide training on subject which are concern with job responsibility
assigned to me to trainees as per calendar schedule.
 Responsible to conduct meeting for mitigation plan which need to
implement.
 Responsible to track the validation and qualification schedule.

PERSONAL PROFILE Father’s Name : Shri Mishri Prasad Gupta


Date of Birth : 16th April 1989
Sex : Male
Marital Status : Un Married
Nationality : Indian
Language Know : English & Hindi
Permanent Address : A.S.Zamania (R.S) , Distt. - Ghazipur
State - Uttar Pradesh, Pin code - 232331

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DECLARATION
I do here by declare that the above and said information are true to the best of my knowledge.

Banshi Dhar Gupta

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