Veeda CR
Analyst
Skills
2 months ago
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Important information
Contract type:
Permanent
Location:
Bengaluru, Karnataka, India
Work mode:
Onsite
Published on:
25 August 2026
What they need
#hiring. Know anyone who might be interested?
Veeda Lifesciences (Veeda Clinical Research) is seeking a passionate "Analyst - Mass Spectrometry"
Experience: 2 to 4 Years
Location: Bangalore
Interested candidates can share an updated CV to [email protected]
JOB DESCRIPTION:
Role & responsibilities:
Experiments:
- Execution of planned experiments/studies using higher-order structure methods.
- Primary structure analysis using amino acid profiling and N-terminal sequencing.
- Amino acid composition analysis using UPLC/HPLC based methods for peptides and proteins
- Secondary structure evaluation using Circular Dichroism (CD) with desalting optimization techniques.
- Amide bond and conformational analysis using FTIR spectroscopy.
- Peptide aggregation and oligomerization studies using SEC and fluorescence-based assays
- Execution of planned experiments/studies using physico-chemical methods.
- Develop advanced LC-MS-based methodologies (ESI, ETD, ECD) for the characterization of protein and peptide products.
- Design and implement integrated analytical strategies by combining chromatography and mass spectrometry techniques. These strategies aim to qualitatively and quantitatively assess product-related variants and impurities. This includes the development of innovative sample preparation methods, with a focus on LC-MS, CEX-MS, and SEC-MS, native MS, HDX as well as the characterization of innovator product batches sourced from various geographical regions to establish a comprehensive quality target profile.
- Lead the development of sophisticated analytical workflows, including multi-attribute methods for post-translational modifications (PTMs), sequence variant analysis, profiling of host cell proteins (HCPs), disulfide bond analysis and shuffling, cell culture metabolite analysis, and glycan profiling.
- Impurity characterization of peptides and comparability assessment with innovator using 2DLC (preferably from Agilent) Qualification of LCMS methods and method transfer according to ICH and regulatory guidelines.
- Fibrillation and amyloid kinetics studies using Thioflavin-T fluorescence assays
- Charge variant/heterogeneity profiling using SCX chromatography
- Hydrophobicity and polarity profiling using RP-HPLC methods.
- Low-level impurity detection (LOQ level) and troubleshooting recovery challenges in peptide analysis.
- Assay, impurities, aggregation, free vs bound drug analysis through different Peptide-related analytical method development
Interpretations:
- Scientific interpretations of processed data (manual/software-driven).
- Stability and degradation pathway assessment of peptides under different stress conditions.
- Regulatory deficiency handling for peptide-based products and analytical justifications
- Establishing quality target profiles according to Q14 and Q2R2/R1
- Scientific interpretations of processed data (manual/software-driven).
Data Generation:
- Sample preparation, data acquisition, data analysis/processing of HPLC/UPLC/LCMS/HRMS/CE based experiments/studies. Preferably on Thermo/Waters/Sciex platforms.
- Expertise on techniques such as CD/FTIR/SEC-FFF-MALS/DSC/DLS as well as different separation technology based on HPLC and UPLC.
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