pankaj bhalerao

Pankaj bhalerao

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location of pankaj bhaleraoPune, Maharashtra, India
Phone number of pankaj bhalerao+91 xxxx xxxxx
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  • Timeline

    May 2008 - May 2011

    Research Associate

    Glenmark Pharmaceuticals
    May 2011 - Jul 2014

    Research Associate

    Accutest Research Laboratories (I) Pvt. Ltd.
    Jul 2014 - Apr 2016

    Research Officer

    Emcure Pharmaceuticals Limited
    Current Company
    Apr 2016 - now

    Deputy Manager

    Cipla
    Patalganga
  • About me

    Deputy Manager at Cipla API R&D

  • Education

    • Prof ramkrishna more arts,commerce & science college, akurdi, pune 44

      2003 - 2006
      B.sc chemistry first class with distinction
    • Modern education society's nowrosjee wadia college arts, science, pune 01

      2006 - 2008
      Master in science m.sc analytical chemistry first class
  • Experience

    • Glenmark pharmaceuticals

      May 2008 - May 2011
      Research associate

      Bioanalytical method development, validation and in blood, Plasma by LC-MS/MS.

    • Accutest research laboratories (i) pvt. ltd.

      May 2011 - Jul 2014
      Research associate

      Bioanalytical method development and method validation drug Product in Blood, serum and Plasma by using LC-MS/MS

    • Emcure pharmaceuticals limited

      Jul 2014 - Apr 2016
      Research officer

      1.Impurity Profiling, Identification of unknown impurity and Quantification of Genotoxic impurity By LC-MS/MS.2.Method development and Validation of Elemental impurities by ICP-MS and ICP-OES.3.troubleshooting and maintenance of Instrument such as LC-MS, ICP-MS, ICP-OES, HPLC and XRD.

    • Cipla

      Apr 2016 - now

      1. Monitoring the activity of Elemental Impurities for Drug Substance and Drug Product by Using ICP-MS and ICP-OES.2. Co-ordinate with Regulatory and Synthetic team for Elemental Impurities and Risk assessments for Final API.Also Selection of Element and Limit as per ICH Q3D.3. Method Development and Validation of Elemental Impurities as per ICH Q3D by Using ICP-MS and ICP-OES.4 Familier with Method transfer activity at Quality control department and guide with respective department.5. Guide the team member for Method development and Validation activity.6. Review the Validation Protocol, Data sheet and Method Validation Report as per GLP compliance.7. Impurity profiling for Raw material, intermediate and Final API by LC-MS and MS-MS with interpretation.8. Identification of unknown impurity in Intermediate and final API by LC-MS.9. Method Development and Optimization of MRM (product ion) MS/MS for API molecule, Impurities.Validate the method as per Validation Protocol of various methods.10. Development of LCMS compatible analytical method using volatile buffers as an alternative for non-volatile phosphate buffer method.11.Familiar with Calibration of Instrument and review report such as LC-MS. HPLC, ICP-MS and ICP-OES.12.Determination of Elemental composition such as C,H,N,S,O &Cl of final API by using CHNSO Analyzer.13 Familier with calibration, maintainace and troubleshooting of CHNSO Analyzer. Show less

      • Deputy Manager

        Jul 2022 - now
      • Assistant Manager

        Apr 2016 - Aug 2022
  • Licenses & Certifications

    • Lean six sigma yellow belt certification

      6sigmastudy - the global certification body for six sigma certifications
      Apr 2021
    • Six sigma and lean:foundetions and principles

      Skillsoft
    • Scrum fundamentals certified (sfc)

      Scrumstudy - accreditation body for scrum and agile
      Apr 2021