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Current Experience

  • Sr Analyst-1
    Since April 2015

Past Experience

  • R&D Sr.Executive
    September 2014 --- March 2015
    Analytical method validation Analytical method tranfer Analytical method validation

  • quality control Sr.Associate
    March 2012 --- September 2014
     Documents reviewing of Stability, Inprocessed & finished,Raw material, packing material, process validation and calibration documents.  Involved ISO 9001-2000 and cGMP Implementation and maintain.  Online regular support to production &Stability with HPLC analysis.  Stability analysis documentation, checking of OOT and OOS Stability study samples analysis as per the protocol.  All the documents submitting to Quality Assurance Department  Daily checking all the lod books of Instruments and Equipments and lab oriented log books.  Effectively preformed Qualitative and Quantitative analysis of In-process samples, Finished products, Process validation samples, Stability and market complaint samples.  Investigates laboratory failures for root cause analysis and assist in the development of appropriate CAPA follow-up strategies to prevent recurrence of failures.  Analyzing, investigating and closure of OOS ,INCIDENTS and OOT documents as possible as transpierce to the auditors.

  • Quality Control Executive
    July 2011 --- February 2012
    this is Eye Drop & sterile plant. i worked in ANDA team worked as a anlayst in all sections like Stability,inprocessed and finished,raw material INSTRUMENTS HANDLED:  HPLC (Agilent 1100&1200 series with Chromeleon software).  HPLC (Waters2895 with Empower 2 software).  HPLC(Shimadzu LC2010CHT with Chromeleon and LC solutions software).  Gas Chromatography ( Shimadzu 17A with Aoc 5000i Head space).  UV-Visible Spectrophotometer (Shimadzu 1700).  Dissolution Apparatus. (ELECTROLAB, LABINDIA, DISTEK).  Disintegration Apparatus.  KF-Titrator.

  • quality control chemist
    March 2008 --- July 2011
    worked as a analyst with Gas chromatography with head space.  Involved ISO 9001-2000 and cGMP Implementation and maintain  Responsible for the preparation and sharing of COA’S of the products being tested.  Documentation related to QC as per current STP,involves in regular in-house cGMP training activities, GLP, and compliance


LinkedIn Assessment :
SOPGMPValidationRegulatory affairsGood Laboratory Practice (GLP)Pharmaceutical IndustryHPLCRegulatory submissionsPharmaceuticsRegulatory RequirementsCleaning Validation


  • Master of chemistry in Analytical chemistry from Sriv enkateswara university in 2015
  • Post graduation diploma in Qualty management from University of Hyderabad in 2011
  • Bachelor's degree in General Studies from Nagarjuna University in 2004
  • Intermediate (maths,physics,chemistry) in Chemistry,Maths,physics from K.N.Junior college in 2000

Area / Region

Bengaluru, Karnataka, India


Driving License
  • No