Sruthi Vasireddy

Lab Quality Supervisor at Tempus Labs, Inc.
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Contact Information
us****@****om
(386) 825-5501
Location
US

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Credentials

  • CITI GOOD CLINICAL PRACTICE COURSE
    CITI Program, A Division of BRANY
    Jan, 2021
    - Nov, 2024
  • THE RCR FOR BIOMEDICAL INVESTIGATORS
    CITI Program, A Division of BRANY
    Dec, 2020
    - Nov, 2024

Experience

    • United States
    • Biotechnology Research
    • 700 & Above Employee
    • Lab Quality Supervisor
      • Dec 2022 - Present

    • United States
    • Hospitals and Health Care
    • 700 & Above Employee
    • Lab Supervisor
      • Jan 2022 - Dec 2022

    • Molecular Infectious Team Lead
      • Aug 2021 - Jan 2022

  • UTHSCT
    • Tyler, Texas Area
    • Reasearch Associate
      • Aug 2011 - Aug 2021

      • Hands-on experience in developing, validating next generation sequencing (NGS) based assays for Mycobacteria isolates using Illumina platform. • Performed genomic DNA isolation, library preparation and analysis using CLC genomics workbench and Galaxy software framework. • Analyzed genomic data by mapping with reference genome determining SNPs, construction of phylogenetic trees of mycobacteria isolates. • Provided training to new laboratory personnel on NGS and sanger sequencing. • Developed, validated and written SOP for adapting the NGS/Illumina workflow in our clinical lab. • Coordinated and executed multiple IRB protocols and MTAs for studies involving human subjects between our lab at UTHSC and collaborators. • Primarily responsible for maintaining Quality Assurance/ Quality Control (QA/QC), Quality Management documentation for the DNA sequencing lab in accordance with Clinical Laboratory Improvement Amendments (CLIA) regulations required for CAP accreditation. • Performed internal audits, proficiency testing, maintenance and validation of equipment, upkeep of SOPs, and calibration of equipment.

    • United States
    • Pharmaceutical Manufacturing
    • 700 & Above Employee
    • Analytical Chemist
      • Oct 2010 - May 2011

      • Developed and optimized a method of reversed phase HPLC for the purification of Paliperidone according to cGMP and FDA guidelines. • Performed degradation studies on Paliperidone samples to check their stability. • Optimized and validated gas chromatography for separation and analysis of other drugs like Darunavir, Barnidipine. • Verified raw materials against quality standards and adherence to specifications. • Prepared and maintained QA/QC records of all the methods developed and validated in our group and reported deficiencies to management.

    • Pharmaceutical Manufacturing
    • 400 - 500 Employee
    • Quality Assurance Trainee
      • Dec 2009 - May 2010

      • Prepared SOPs for the procedures carried out in the laboratory. • Tested routine samples using HPLC and GC. • Handled UV-Visible spectrophotometer, Infrared Spectrophotometer. • Prepared SOPs for the procedures carried out in the laboratory. • Tested routine samples using HPLC and GC. • Handled UV-Visible spectrophotometer, Infrared Spectrophotometer.

Education

  • Sri Ramachandra Medical College and Research Institute
    Master's degree, Master of pharmacy (Quality Assurance)
    2009 - 2011
  • Sri Ramachandra Medical College and Research Institute
    Bachelor of Pharmacy
    2005 - 2009

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