Riya Rakshit
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Riya Rakshit Email & Phone Number

Scientist Analytical Development at Aurigene Pharmaceutical Services Limited
Location: Ahmedabad, Gujarat, India 11 work roles 2 schools
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Role
Scientist Analytical Development
Location
Ahmedabad, Gujarat, India
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Riya Rakshit is listed as Scientist Analytical Development at Aurigene Pharmaceutical Services Limited, a with 143 employees, based in Ahmedabad, Gujarat, India. AeroLeads shows a matched LinkedIn profile for Riya Rakshit.

Riya Rakshit previously worked as Scientist I at Kashiv Biosciences Llc and Associate Scientist II at Kashiv Biosciences Llc. Riya Rakshit holds Master Of Engineering - Me, Biotechnology from Birla Institute Of Technology And Science, Pilani.

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Aurigene Pharmaceutical Services Limited

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About Riya Rakshit

As a seasoned Analytical Method Development professional with over 8 years of enriching experience across esteemed Biopharma organizations and academia, I am deeply committed to advancing biotechnology and pharmaceutical sciences through meticulous scientific endeavors.🧪 Skills: My expertise spans a spectrum of cutting-edge techniques, including LC-MS (Orbitrap Q Exactive Plus), Biopharma Finder, Proteome Discoverer, Mascot, Xcalibur, Chromeleon, HPLC, UHPLC, AUC (Optima), UV CD, DLS, DSC, SEC MALS, Fluorescence and UV Spectroscopy, Free Thiol Estimation, and more. My prowess extends beyond the lab, encompassing QMS, URS, Equipment Qualification, Impact and Risk Assessment, and Audit Readiness.🔬 Experience:Scientist I at Kashiv Biosciences: Spearheading the development, qualification, and transfer of diverse Mass Spectrometry methods for Monoclonal Antibodies, Fusion Proteins, and Peptides. I excel in Impurity Characterization, Peak Identification, Glycan Profiling, and Subunit Mass Analysis, contributing to crucial bio-similarity studies and stability assessments.Research Associate at Intas Pharmaceuticals: Proficiently navigating protein characterization through an array of advanced techniques, including AUC, CD, DLS, DSC, Fluorescence Spectroscopy, UV Spectroscopy, and various chromatographic methodologies. My roles have encompassed method development, regulatory support, and instrumental in-house establishment, all while being instrumental in various studies and submissions.Junior Research Associate at Bharat Biotech: Contributing to vaccine efficacy analysis and downstream processing, I have achieved process optimization, protein expression, purification, and characterization, along with in-vivo studies. 📚 Education: Armed with a Master of Engineering with majors in Biotechnology from BITS Pilani and a Bachelor of Technology from West Bengal University of Technology, I have consistently excelled academically, earning recognition through presentations at international conferences.I am not only a hands-on scientist but also a strategic thinker who has been recognized for contributions to cost-saving initiatives, regulatory compliance, and driving impactful research projects. With an innate ability to collaborate across disciplines, I am eager to explore new challenges and contribute meaningfully to the forefront of biopharma innovation.Feel free to connect with me for collaborations, discussions, or opportunities in the realm of analytical method development, biopharma research, and beyond!

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Aurigene Pharmaceutical Services Limited
Aurigene Pharmaceutical Services Limited
Scientist Analytical Development
Employees
143
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11 roles

Riya Rakshit work experience

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Scientist I

India

Key Responsibilities:➤Method Development and Qualification: Developing and qualifying methods using Mass Spectrometry (Orbitrap) for various applications, such as intact mass analysis, reduced mass analysis, subunit mass analysis, top-down sequencing, peptide mapping, and disulphide bridge mapping. Optimizing and validating these methods to ensure accurate and reliable results.➤Impurity Characterization: Characterizing impurities in monoclonal antibodies, fusion proteins, and peptides using Mass Spectrometry techniques.➤Peak Identification and LC Method Development: Supporting the LC team by identifying and interpreting peaks in chromatographic data. Assisting in the development and optimization of LC methods, ensuring efficient separation and detection of analytes.➤Software Utilization: Utilizing software platforms such as Biopharma Finder, Proteome Discoverer, Mascot, Xcalibur, and Chromeleon for data processing, analysis, and interpretation.➤Molecule Analysis: Handling and analyzing various biomolecules, including monoclonal antibodies, fusion proteins, and peptides, using Mass Spectrometry techniques.➤Multiple Attribute Method Development: Developing multiple attribute methods to assess various post-translational modifications (PTMs) and glycans in biomolecules. Optimizing methods to ensure comprehensive evaluation of PTMs and glycans, contributing to product quality control.➤Bio-Similarity Studies and Stability Studies: Contributing to bio-similarity studies to assess the comparability of biopharmaceutical products. Participate in stability studies to evaluate the long-term stability and degradation patterns of biomolecules. ➤Equipment Installation and Qualification: Supporting the installation and qualification of Mass Spectrometry equipment. Preparing necessary documents and reports, ensuring adherence to standard operating procedures and regulatory requirements.

Jan 2023 - Oct 2023

Research Associate

Ahmedabad, Gujarat, India

Key Responsibilities:➤Method Development and Qualification: Developing and qualifying methods for protein characterization using a variety of techniques, including Analytical Ultra Centrifugation (AUC), Far and Near UV Circular Dichroism (CD), Differential Scanning Calorimetry (DSC), Dynamic Light Scattering (DLS), Fluorescence Spectroscopy, UV spectroscopy, Free Cysteine estimation, SEC MALS (Multi-Angle Light Scattering), and various chromatography techniques (CEX, SEC, RP) using HPLC and UHPLC. ➤Molecule Handling: Handling a range of molecules, such as Adalimumab, Ranibizumab, Bevacizumab, GCSF, Peg GCSF, Icatibant, and Virus particles. Performing characterization and analyzing on these molecules using the developed methods and techniques.➤Planning and Execution of Studies: Playing a key role in planning and executing studies, including stability studies, hold time studies, and force degradation studies. Contributing to experimental design, data analysis, and interpretation to assess product stability, degradation pathways, and potential challenges.➤Regulatory Support: Supporting the HOS (Higher Order Structure) and Chromatographic teams in regulatory submissions, bio-similarity assessments, and addressing regulatory queries.➤In-house Method Development and Cost-Cutting: Contributing to cost-cutting efforts by developing in-house methods that were previously outsourced. Optimizing and establishing analytical techniques, such as using the Beckman Coulter OPTIMA AUC, to bring efficiency and cost-effectiveness to the analytical development process.➤QMS Elements and Recognition: Handling Quality Management System (QMS) elements related to analytical development and demonstrating compliance with relevant guidelines and regulations.

May 2019 - Nov 2021

Junior Research Associate

Hyderabad, Telangana, India

Key Responsibilities:➤Clone Development and Protein Expression: Participating in the development of clones for the vaccine candidate. Conducting protein expression experiments in shake flasks to produce the target protein. Optimizing expression conditions to achieve high protein yield.➤Purification and Characterization: Utilizing NGC Chromatography for the purification of the vaccine candidate protein. Implementing purification protocols to isolate and purify the protein of interest. Performing characterization studies using techniques such as Circular Dichroism (CD), Differential Scanning Calorimetry (DSC), and Dynamic Light Scattering (DLS) to evaluate its structural properties and stability.➤In-vivo Mice Studies: Planning and conducting mice studies to assess the efficacy of the vaccine candidate. Optimizing the dosage of the vaccine for maximum immunogenicity. Analyzing immunogenicity responses in mice to evaluate the potential effectiveness of the vaccine in combating the deadly carcinoma.➤Downstream Processing Protocol Standardization and Scale-up: Standardizing the downstream processing protocol for the vaccine candidate. Developing and optimizing the purification process to ensure reproducibility and efficiency. Successfully scale up the process to a 10 L batch, enabling larger-scale production of the vaccine candidate.➤Expression and Purification of Yeast Recombinant Antigen: Handling the expression and purification of a yeast recombinant antigen. Standardizing yeast growth kinetics and transformation techniques, such as electroporation, to achieve efficient protein expression. Purifying the recombinant antigen to obtain a high-quality and pure protein product.➤Career Advancement: Recognized for success with the vaccine development process hence, promoted from a Trainee to a Research Associate. This promotion acknowledges my contributions and achievements in successfully advancing the vaccine development project.

Jun 2017 - May 2019

Project Assistant

Hyderabad, Telangana, India

Key Responsibilities:➤Expression and Purification: Successfully expressed and purified CheY proteins using affinity chromatography techniques, specifically with AKTA prime system. This involved optimizing expression conditions, protein extraction, and purification methods to obtain high-quality CheY protein samples.➤Analysis of Protein Structure: Employed various analytical techniques to analyze the structure of CheY proteins in the presence of a crowding agent. These techniques include:➤Circular Dichroism (CD): Used to assess the secondary structure and conformational changes in CheY proteins. CD spectroscopy provides information on protein folding, stability, and interactions.➤Differential Light Scattering (DLS): Utilized to measure the size distribution and aggregation state of CheY proteins. DLS can indicate protein-protein interactions and the effects of crowding agents on protein stability.➤Dynamic Scanning Calorimetry (DSC): Employed to investigate the thermal stability and folding/unfolding behavior of CheY proteins. DSC measures the heat capacity changes associated with protein conformational transitions.➤Fluorescence and UV Spectroscopy: Employed fluorescence spectroscopy to probe the tertiary structure and tryptophan environment of CheY proteins. UV spectroscopy was used for protein quantification and determining the concentration of CheY samples.➤Protein Quantitative/Qualitative Assay: Utilized assays to quantitatively determine the concentration of CheY proteins. This helps in accurate sample preparation and data analysis.➤Analysis of Crowding Agent Effects: Investigated the influence of the crowding agent on the structure and stability of CheY proteins. By comparing the results obtained in the presence and absence of the crowding agent, you have assessed its impact on protein conformation, folding, aggregation, and overall stability.

Aug 2016 - Oct 2016

Teaching Assistant

• Teaching Assistant in Department of Mathematics• Teaching Assistant in Work Integrated Learning Programs• Teaching Assistant in Department of Economics and Finance• Teaching Assistant in Department of Biological Sciences

Aug 2014 - Jun 2016

Research Intern

East India Pharmaceuticals

Industrial training on production of Quin-Iodochloro IP and colloidal Iron

Jun 2013 - Jul 2013

Research Intern

Bidhan Chandra Krishi Vidyalaya

Standardizing amplified restriction fragment length polymorphism of sesame in agarose gel• Construction of SSR enriched genomic library by different methods.• Identification of valid SSR, ISSR and RAPD markers in sesame.• Morphological and molecular characterization of a core collection of sesame.

Jan 2013 - Feb 2013

Research Intern

Chitaranjan National Cancer Institute

Kolkata Area, India

Cytotoxic effect of Madhuca indica extracts on HCT-116 colon carcinoma cell line.Cell revival and maintenance, Cytotoxicity assay, Viability assay, Immunofluorescence staining, Hematoxylin Staining for Apoptotic Nuclei dectection, Western Blot

Oct 2012 - Nov 2012
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2 education records

Riya Rakshit education

Bachelor Of Technology - Btech, Biotechnology

Efficacy of in-situ formulated silver nanoparticle as an antibacterial agent on the leaf extract of Azadirachta indica • Ranked 3rd.

FAQ

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What company does Riya Rakshit work for?

Riya Rakshit works for Aurigene Pharmaceutical Services Limited.

What is Riya Rakshit's role at Aurigene Pharmaceutical Services Limited?

Riya Rakshit is listed as Scientist Analytical Development at Aurigene Pharmaceutical Services Limited.

Where is Riya Rakshit based?

Riya Rakshit is based in Ahmedabad, Gujarat, India while working with Aurigene Pharmaceutical Services Limited.

What companies has Riya Rakshit worked for?

Riya Rakshit has worked for Aurigene Pharmaceutical Services Limited, Kashiv Biosciences Llc, Intas Pharmaceuticals Ltd. (Biopharma Division), Bharat Biotech International Limited, and Bits Pilani, Hyderabad Campus.

Who are Riya Rakshit's colleagues at Aurigene Pharmaceutical Services Limited?

Riya Rakshit's colleagues at Aurigene Pharmaceutical Services Limited include Madhavi Shelar Pawar, Suman Reddy, Poonam Nale, Srikanth Karanki, and Mainak Ganguly.

How can I contact Riya Rakshit?

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What schools did Riya Rakshit attend?

Riya Rakshit holds Master Of Engineering - Me, Biotechnology from Birla Institute Of Technology And Science, Pilani.

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