Balaji - Railway Man - Hyderabad, Andhra Pradesh, India

Matta Balaji

Hyderabad, Andhra Pradesh, India

Services

Railway Man

  • Full time
  • Part time
  • One time
  • Contract
  • Temp

Work History

Sr.Executive

Aurobindo Pharmaceutical Limited (Formulation), Unit III, Bachupalli, Hyderabad.

From August 2009

CAREER PROFILE:

 Working “Q. C. Sr. Executive” (E4) in
M/s. Aurobindo Pharmaceutical Limited (Formulation),
Unit III, Bachupalli,
Hyderabad.
From Aug 2009 –to till date
(MHRA, TGA, ANVISA, MCC US -FDA, WHO & GMP Certified Company)


 Worked as “Q. C. Sr. ANALITICAL CHEMIST” in M/s. Hetero Drugs Limited (Formulation). Baddi
From Sep 2007 – 2009 (A WHO & GMP Certified Company.)

 Worked as “Q. C. Asst. CHEMIST” in Yelluri&Supra (Formulation) Pharmaceutical Ltd, IDA, Bollaram. Hyd. From July 2006 to Sep 2007

Present working position: Sr. Executive (E4)
Strengths
1. GLP
2. cGMP
3. Team Motivation
4. Result oriented
5. Updating knowledge as per current revisions of guide lines.
6. Analytical Method Validation of Residual solvents by GC.
. 7. Well experienced in handling of HPLC, GC, UV, IR, Dissolution and KF Titrator .

Area/ Section Worked:
 Raw Material, Finished Product, In process, Process Validation for (Tablets/ Capsules/ Dry syrups / Oral Solutions )
Present Job Responsibilities:
 To plan the daily activity to the Analysts.
 To communicate and sharing of data to the Q.A & RAD.
 Preparations of ATDS and review.
 Monitoring of day to day functioning of stability chambers.
 Ensure the testing of samples at outside lab and Micro Lab.
 Responsible for method validation, process validation. Cleaning Validation, Cleaning Method Validation & Hold time Study, Indirect AMT , Direct AMT, Product Development, Multimedia Profiles, Equipment Validation
 Ensure that the availability of WSTD’s, Reference STD’s, HPLC Columns and Chemicals.
 Responsibility of Maintaining all QC records as per ISO Standards.
 Responsible for the sampling and analysis of raw Materials Trouble shooting of HPLC and GC instruments during the course of analysis.
 Initiating and implementing the GLP and cGMP activities in the departments.
 Monitoring the Calibrations of Instruments and taking care (by maintaining the requ

SR.Excutive

Aurobindo Pharma

August 2009 - August 2009

Sr. Executive

E4

August 2009 - August 2009

MHRA, TGA, ANVISA, MCC US -FDA, WHO & GMP Certified Company)


Worked as “Q. C. Sr. ANALITICAL CHEMIST” in M/s. Hetero Drugs Limited (Formulation). Baddi
From; (A WHO & GMP Certified Company.)

Worked as “Q. C. Asst. CHEMIST” in Yelluri&Supra (Formulation) Pharmaceutical Ltd, IDA, Bollaram. Hyd

Sr. Executive

Aurobindo Pharma

August 2009 - August 2009

Strengths
GLP
cGMP
Team Motivation
Result oriented
Updating knowledge as per current revisions of guide lines.
Analytical Method Validation of Residual solvents by GC.
.
Area/ Section Worked:
Raw Material, Finished Product, In process, Process Validation for (Tablets/ Capsules/ Dry syrups / Oral Solutions )


Known Techniques:
HPLC:
WATERS 2695(With EMpower-2 soft ware)
SHIMADZU Lc-2010 AHT, Lc-2010 AHT with PDA, Prominence (With LC Solution, Class VP Soft wares
GC
Shimadzu with LC Solution &
Agilent with Chemstation software

Dissolution Apparatus (Electro Lab, Lab India, Parma Tester, Distack)
Rudolph-Autopolarimeter
Karl Fischer titrator (Metrohm)

Sr.Executive ( QC Process Vallidation)

Aurobindo Pharma Limited

From August 2008

Sr.EXECUTIVE

Aurobindo Pharma

July 2006 - July 2006

Aurobbindo pharama Ltd

Qualifications & Certifications

M.Sc., (Organic Chemistry)

SV College

Little Angels High School, Tirupathi

SSC

I.P.E

B.Sc

Dairy Science

M.Sc

Bojju College, Barkathulla University

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