Sarthak Suvojit Das

Experience

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  Vellore Institute of Technology

  Aug 2019 - Dec 2020

  Dr. Ramesh N. Lab, Antibiotic Resistance and Phage Therapy Lab

  Antimicrobial Resistance (AMR) of Methyicillin Resistant Staphylococcus Aureus infection

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  CSIR India

  Jun 2020 - Aug 2020

  Summer Intern

  Guide - Dr. Ashwini ChauhanTopic - Review on Gram Positive Bacterial biofilms: role of persistersCSIR SRTP 2020 CSIR-North East Institute of Science & Technology

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  Heredity BioResearch

  Jun 2020 - Sept 2020

  Research Intern

  Guide - Dr. Pratyush Kumar DasTopic -Iodine and associated problems in Humans

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  CSIR-Indian Institute of Toxicology Research, Lucknow

  Jun 2020 - Aug 2020

  Summer Intern

  Guide - Dr. KM AnsariTopic - Review on Future Prospects in India emerging Food AdulterationCSIR SRTP 2020 CSIR-Indian Institute of Toxicology Research

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  Xcellogen Biotech India Pvt Ltd

  Jul 2020 - Aug 2020

  Internship Trainee

  Online Internship on Advanced Medical Biotechnology

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  Society of Chemical and Synthetic Biology (SCSB)

  Dec 2020 - Jun 2021

  Member
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  Christian Medical College Vellore

  Dec 2020 - May 2021

  Research Intern

  Department of Clinical Microbiology Dissertation Project under Dr. Balaji V.

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  Yapan Bio

  Jun 2021 - Nov 2022

  Executive

  Quality Control Analytical Development1. Analysis of VLP Samples , Different Protein Antigen Samples by SDS PAGE , Western Blot , BCA Protein Estimation , Lowry Method , Bradford and ELISA .2. Preparation of SOPs , STPs .3. Basic knowledge of QMS OOS OOT , CAPA , Deviations , Change Control and Risk Assessment.4. Analysis of RnD Samples ( Assay related substances, Osmometer , UV Visible Spectrophotometer, Water Content Endotoxin )5. Responsible for online Documentation Analysis done. 6. Operations of calibration of analytical instruments.7. Responsible for Instrumental Analysis of studies samples and documentation as per In-house procedure.8. Responsible for Instrumental analysis of method validation.9. Preparation and implementation of GLP in Laboratory 10. Analyse analytical data , comprehend results and identify issues.11. Responsible for preparation of storage usage of solutions.12. Method Development Designing and developing analytical methods to assess the quality, purity, potency, and stability of raw materials, intermediates, and finished products. This includes selecting appropriate analytical techniques, optimizing parameters, and validating methods according to regulatory guidelines.13. Method Validation Conduct validation studies to demonstrate the accuracy, precision, specificity, linearity, and robustness of analytical methods. This involves designing validation protocols, performing experiments, analyzing data, and preparing validation reports in compliance with regulatory requirements (e.g., ICH guidelines). Show less

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  Panacea Biotec

  Nov 2022 - Mar 2023

  Scientific Officer

  Quality Control Immunochemistry Department 1. Assay Development Developing and validating immunochemical assays used for product testing, such as enzyme-linked immunosorbent assays (ELISA), western blotting, immunohistochemistry, flow cytometry, and other immunoassays (Hepatitis-B Surface Antigen, Recombinant Hepatitis B, Polysaccharide vaccines) combination vaccines.2. Handling of QMS Elements (Incidents, Deviations, CAPA, Change Control, OOT & OOS).3. Determination of Residual Protein content by ELISA4. Good with immunological in vitro QC testing for the following vaccines: Diphtheria, Haemophiles type b conjugate, pertussis.5. Kinetic Turbidimetric endotoxin test for Water for injection Samples, Pure Steam Samples.6. Carry out operations in accordance with important documents such as Standard Operating Procedures, Validation Protocols, Laboratory Control Records, and Log Sheets. doing studies in accordance with WHO's GMP and GLP criteria.7. Responsible for following of calibration schedule of the lab , lab instruments as per master plan.8. Analyse stability samples of development trails .9. Having knowledge of ALCOA+.10.Instrumentation Maintenance Overseeing the maintenance, calibration, and troubleshooting of immunochemistry-related instrumentation and equipment, such as plate readers, spectrophotometers, liquid handling systems, and automated immunoassay platforms. Show less

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  Premas Biotech

  Mar 2023 - Jun 2024

  Executive

  Quality Control and Analytical Department1. Protein characterization using electrophoretic techniques like SDS-PAGE, Native PAGE, Western blotting, etc., and quantitative methods like Bradford, BCA, etc.2. BET Testing of Cleaning Validation Samples and In-process Samples of different Products.3. Quantitative Purity Analysis by RP UPLC (Agilent Systems) , Handling SEC-HPLC, and RP-HPLC by Agilent Infinity Systems (Open Lab CDS Software) .4. SOP procedure updating and Documentation.5. Method Development and Validation Developing and validating analytical methods to accurately assess product quality, ensuring that these methods are reliable, reproducible, and compliant with regulatory standards.6. Data Analysis and Reporting Analyzing test results and generating comprehensive reports to document findings, trends, and deviations from quality standards. This information is crucial for identifying areas of improvement and making data-driven decisions to enhance product quality.7. Equipment Calibration and Maintenance Overseeing the calibration, maintenance, and troubleshooting of analytical equipment to ensure accurate and reliable test results. This involves scheduling regular maintenance, performing calibration checks, and promptly addressing any equipment malfunctions or issues.8. Documentation and Record-Keeping Maintaining accurate records of quality control activities, test results, and related documentation in compliance with regulatory requirements. This documentation serves as a critical reference for auditing purposes and provides traceability throughout the product lifecycle.9. Continuous Improvement Participating in continuous improvement initiatives to optimize quality control processes, enhance efficiency, and drive innovation. This may involve conducting root cause analyses, implementing corrective and preventive actions, and participating in cross-functional teams to address quality-related issues. Show less