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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 science)" rel="nofollow">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

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