Ashok Choudhary

Experience

• 

  Veeda Clinical Research

  Sept 2017 - Mar 2021

  •To search the literature for assigned molecules from various research papers, research articles, internet websites for bioanalytical method development.•To prepare the solutions which using for bioanalytical samples preparation, for equipment (LC-MS/MS).•To process the bioanalytical samples (Plasma, Serum, Blood, Urine, tisssue etc.) during bioanalytical method development, method validation, project sample analysis by using Solid Phase Extraction, Liquid- Liquid Extraction, Protien Precipitation and Hybridge extraction techniques.•To perform the operation, calibration and performance verification of general equipments used in bioanalytical laboratory (e.g. Analytical balance, Microbalance, PH Meter, Pipettes, Centrifuges, Evaporators, SPE equipments, Rotospin Extractor, Liquid-liquid Extractor etc.)•To perform the operation, calibration, performance of the chromtographic device LC-MS/MS (API2000, API3000, API3200, API4000 instruments by using Analyst software).•To records the bioanalytical experimental activities in relevant log books, Method Book, controlled documents.•To maintain the calibration and maintenance records of equipments.•To Prepare, maintain and update the equipments labels. •To prepare and review the Method SOP, Bioanalytical Method Validation Protocol, Bioanalytical Study Plan, Amendment as per in-house SOPs, current regulatory guidelines under the guidance of Group Leader and Senior Group Leader.• To Review the bioanalytical raw data thats generated during method development, method validation and project sample analysis.•To draft the deviation, file note, unforeseen events for bioanalytical experiment failure or unexpected results found. •To guide and provide the training to juniors for equipments handling, samples preparation and documentation.•To provide response of QC and QA queries/observations in bioanalytical data and laboratory. Show less •To Review the Method Book for Bioanalytical Method Development.•To Review the Method SOPs, Bioanalytical Method Validation Protocols, Bioanalytical Study Plan with compliance to in-house SOPs and current regulatory guidelines requirements. •To Review the Bioanalytical Method Validation, Project Sample Analysis raw data. •To Review the Draft Report of Bioanalytical Method Validation and Project sample analysis. •To Review the Log Books used for recording the relevent entries during bioanalytical samples preparation in the laboratory.•To Review the calibration, maintainance and performance verification documents of an equipments used in Bioanalytical Lab. •To Review the Installation Qualification, Operational Qualification, Performance Qualification data of Software and LC-MS/MS.•To Review the Deviations (Protocol/SOP), Change control Forms. •To Review the Personnel Training Records data file of Lab personnel.•To Maintain and issue the controlled Documents to Lab personnel. •To ensure the quality of Protocols, raw data and draft report by co-ordination with analysts, group leaders, senior group leaders, report writers and QA auditors.•To cunduct the SOPs and Guidelines training to freshers and new joiny in bioanalytical department.•To provide response of lab round observation, raw data and protocols audit report to QA department.•To archive, retrieve and re-archive the raw data.•To maintaining the project tracking records. Show less

  • Research Associate- Analyst

    Jan 2020 - Mar 2021

  • Bioanalytical Quality Monitor (QC Reviewer)

    Sept 2017 - Jan 2020
• 

  Accutest Research Laboratories (I) Pvt. Ltd.

  Apr 2021 - Jun 2021

  Research Associate- Analyst

  Bioanalytical Department

• 

  Lambda Therapeutic Research

  Jul 2021 - Jun 2022

  Research Associate- Analyst

  Bioanalytical Department

• 

  Syngene International Limited

  Jun 2022 - now

  Discovery Biology- In Vivo- Bioanalytical- Drug Metabolism and Pharmacokinetics (DMPK)

  • Associate Scientist

    Oct 2024 - now

  • Senior Research Associate

    Jun 2022 - Oct 2024