CURRICULUM VITAE

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CURRICULUM VITAE
Mr.JAGDEV BEHERA
M-Pharm
E-mail: [email protected]
Mobile no: 09975517619
OBJECTIVE:
To pursue a challenging career in your esteemed organization, I would also like to
make positive contribution towards promoting team spirit and own professional
growth.
PROFESSIONAL PROFILE:
Working as section head in mabpharm,Goa in QC biochemistry dept from august
2012 to till date.
Worked as Executive in Q .C. department, Wockhardt Biotech Ltd, Aurangabad,
Maharashtra, from November 2009 to August 2012
Training experience in Serum Institute of India PUNE from June 2008 to Septmber
2009
TECHNICAL SKILL:
 HPLC: Agilent System with EZchrom & Chemstation Software. Also
worked on RRLC (Rapid Resolution Liquid Chromatography). Knowledge of
calibration and trouble shooting.
 AAS: GBC Scientific with Avanta Software
 UV Spectrophometer (Shimazdu)
 G C (Agilent)
 Analysis and determination of impurities profile of protein drug by HPLC.
 Determination of potency of protein drug by HPLC.
 Development of analytical method for API and Injectable.
 Analytical method validation HPLC Methods.
 Molecular Biology work-SDS PAGE(Reducing and Non-reducing),Isoelectric focusing, RT-PCR, Estimation of glucose in media.
JOB RESPONSIBILITIES:
Development and Validation
Preparation of protocol for method development for RP chromatography, IonExchange chromatography for bio molecule and small molecule.
Development of RRLC Method from HPLC method.
Validation of analytical method.
 Planning of daily work in a organize manner to get maximum output.
Batch release and Stability
 Planning and execution of sample for finished product ,API.
 Preparation of stability protocol and planning of stability study.
 Preparation and review of specification.

Looking after In process and batch release of API and Finished product.
 Conducting different study as per regulatory market requirement
For finished product.
Calibration.
 Taking care of calibration of all the instrument of QC lab and review of the
same.
Review and GLP Activities
 Review of chromatographic data ,Review of SOP and Other Document.
 Act as active member in Internal Audit.
 Updating of GLP requirement and training impart for the same.
REGULATORY AUDIT:
 Faced regulatory audit like FDA, ANVISA
 Working on Domestic as well USP, BP & Ph. Eur specifications.
AREA OF INTEREST:
Quality Control
Analyticaldevelopment
ACADEMIC BACKGROUND:
Class
Academic year
Board/University
Grade
M-Pharm
2007-09
BharatividyapeethUniversity,
PUNE
First class
GATE
B-Pharm
2007
2002-06
IIT, Kanpur
93 Percentile
B.P.U.T., Orissa
First class
COMPUTER LITERACY:
 Microsoft office 97-2003/2007
 Knowledge of Internet
 Power point presentation.
PROJECT WORK(M.PHARMA)
Synthesis,
purification
and
characterization
of
anti
diabetic
drug
“EXENATIDE”
SUMERY OF WORK-Synthesis of protein, purification by HPLC,BIOEFICACY Study in mice(estimation of glucose in serum)
PERSONAL INFORMATION:
 Father’s Name: Pitabas Behera
 D.O.B-25/05/1983
 Languages
known:
English, Oriya
PERMANENT ADDRESS:
At: Siula Post: Siula
Via: Pipili, Dist: Puri
 Key
Strength:
Patience
Hard work
Hindi,
 Marital Status:
Single
 Religion:
Hindu
 Nationality:
Indian
and
State: Orissa, 753104
DECLARATION:
To the best of my knowledge and belief this curriculum vitae correctly describes
myself, my qualification and my experiences. I understand that my willful
mistake described here in may lead to my disqualification or dismissal if engaged.
Place:
Date:
Signature: Jagdev Behera
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