jitin chauhan

E.mail adhi1z@r.postjobfree.com

Mob.no-099********

Addes-vill-khedily, post-Bahadrabad,Dist-Haridwar(U.K)

OBJECTIVE:

To pursue a career in an esteemed organization and to nurture my scientific outlook by constant learning to carve a niche in whatever I undertake.

EXPERINCE:

Current – Zydus Cadila as Ho Executive Feb 2016 to Till Date.

Previous --

1. Pfizer India Ltd. as Officer Aug 2012 to Feb 2016.

2. Jubilent life sciences ltd., as officer in R.M. (Dec.2010- July 2012)

3. Dr.John, s Lab Pvt.ltd. Sidcul (Haridwar), (Dec.2008-Dec.2010).

EDUCATIONAL QUALIFICATIONS:

Sr.no.

Qualification

Board/University

Division

Year of

Passing

1

M.Sc.

(Pharmaceutical

Chemistry)

*SBSPGI of Biomedical Sc.

and Research, Balawala, ( *H.N.B.G.U) Uttrakhand

I

2008

2

B.Sc

G.K.V

II

2006

3

4

12th

10th

U.A Borad

U.P Borad

II

II

2002

2000

*SBSPGI (Sardar Bhagwan Singh Post Graduate Institute)

*HNBGU (Hemwati Nandan Bhuguna Gharwal University)

JOB RESPONSIBILTIES:

Zydus Cadila Ltd.

1. Handling the all QC instrument and Calibration.

2. Preparation the STP/SPECIFICATION according to pharmacopeia.

3. Stability and FG section planning.

4. Review of data and trending of stability data.

5. Preparation the STP/SPECIFICATION of Stability Samples& withdrawal tracker.

6. To prepare qualification protocol & execute the protocol.

7. To prepare Annual Product Review Report.

8. Document issuance and retrieval in Quality Assurance Department (BPR, BMR and quality control documents).

9. Handling of change control, deviation and incidents in quality control/ Assurance department.

10. Review of BMR,BPR and Other Documents

Knowledge of Validation activity.

1.Stability Chambers

2. HVAC

3. Incubators

Pfizer India Ltd.(Zoetis India Ltd):

1. Handling the all QC instrument and Calibration.

2. Preparation the STP/SPECIFICATION according to pharmacopeia.

3. Stability sample Analysis & Data trending& Planning.

4. Preparation the STP/SPECIFICATION of Stability Samples& withdrawal tracker.

5. To prepare qualification protocol & execute the protocol.

6. To prepare Annual Product Review Report.

7. Document issuance and retrieval in Quality Assurance Department (BPR, BMR and quality control documents).

8. Handling of change control, deviation and incidents in Quality control/ Quality Assurance

Audits Faced

USFDA

MHRA

EU GMP

TGA

ANVISA-BRAZIL

MCC

MOH- IRAN

MOH- SUDAN

WHO-GMP

SFDA

INJUBLIENT LIFE SCIENCES

RM samples analysis and trend analysis for the drug products as per application SOPs and STPs.

Raw material testing (excipients and API).

Ensuring upkeep & maintenance, calibration and troubleshooting of equipments.

Handling of working standards and their standardization

Preparation,standardization of volumetric solutions

Any other responsibility assigned by HOD.

IN DR.JOHNS LAB PVT LTD.

Complete analysis of finished products, Semi-finished products, Stability samples and (tablet, capsule, & syrup).

TECHNIQUES EXPERTISE IN:

Chromatographic techniques

High-Performance Liquid Chromatography (HPLC).

GC (Perkin Elmer, Agilent)

Spectral techniques

UV-Visible Spectrophotometer and Infrared Spectroscopy (-IR),

KF apparatus, Polarimeter,Autotiter,Seive Analysis&Particle size by Alpine air jet

Disintegration apparatus.

INSTRUMENT HANDLING:

HPLC

WATERS ALLIANCE :- E-2695 with Empower -2&3 software.

SHIMADZU: - L.C Solution software.

AGILENT: - 1200 Series with chemastatin software.

UV-VISIBLE SPECTROPHOTOMETRY

Shimadzu 1700 and UV-2450

FTIR :- Perkin Elmer

POLARIMETER :- Perkin Elmer

KARLFISHER, AUTOTITRATER :- Metrohm

DISINTIGRATION

REFRACTOMETER

COMPRESSION TESTER FOR PACKING

BUSTING STRENGTH TESTER

RUBPROOFNESS TESTER

L.P.C

PERSONAL DETAIL:

Name : JITIN CHAUHAN

Father's Name : CHARAN SINGH CHAUHAN

Mother's Name : USHA CHAUHAN

D.O.B. : 10th JULY 1985

Marital status : Married

Gender : Male

Nationality : Indian

Languages Known : Hindi, English

Hobbies : Cricket, Football.

Blood Group : AB +ve

JITIN CHAUHAN

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