Madhu Kodipelli

Scientist -ll Bioanalytical at Ecron Acunova
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Contact Information
us****@****om
(386) 825-5501
Location
India, IN
Languages
  • English -
  • Hindi -
  • Telugu Native or bilingual proficiency

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Experience

    • Germany
    • Pharmaceutical Manufacturing
    • 100 - 200 Employee
    • Scientist -ll Bioanalytical
      • Mar 2022 - Present

      Bioanalytical QC and Compliance  GLP compliance support (perform/review calibrations)  All study related QC activities are performed as per in-house SOPs, STPs, Protocol and Plans. Online/In-process review of prerequisites of MV (Literature, Cmax, Pharmacokinetic and metabolite details) and review of MV, bioanalytical processes associated data and data for ALCOAC.  Verification of matrix, study sample receipt, handling, storage, and usage.  Review of BA reports against raw data.  Data compilation and review.  For Bioanalytical ANDA and eCTD internal coordination and review.  Review of training records of new joiners and relieving employees  Event tracking and categorization for monthly meeting Track sheet management  Internal forms/log issue management  General logbooks verification  Column management  Working standard review and acceptance Show less

    • India
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Executive bioanalytical
      • Apr 2018 - Mar 2022

      Diligently Handling and involved in various LC-MS (Triple quadrupole) Method Development, Method Validation and Subject Sample Analysis of various molecules  Coordination with pharmacokinetics, clinical departments and principal and co-investigators while preparation of Bioanalytical Study Reports and compilation of various data  Extensive literature search, Documentation, Reporting and compiling the results for Method Validation and Subject Sample Analysis as per SOP Diligently Handling and involved in various LC-MS (Triple quadrupole) Method Development, Method Validation and Subject Sample Analysis of various molecules  Coordination with pharmacokinetics, clinical departments and principal and co-investigators while preparation of Bioanalytical Study Reports and compilation of various data  Extensive literature search, Documentation, Reporting and compiling the results for Method Validation and Subject Sample Analysis as per SOP

    • Pharmaceutical Manufacturing
    • 500 - 600 Employee
    • Executive
      • Apr 2016 - Apr 2018

Education

  • Kakatiya University (University College of Pharmaceutical Sciences)
    Master's in pharmacy, Medicinal and Pharmaceutical Chemistry
  • Kakatiya University
    Bachelor of Pharmacy (B.Pharm.), Medicinal and Pharmaceutical Chemistry

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