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Associate Scientist / Senior Research Associate – Translational Medicine (Genomics)

Syngene
Syngene
2-6 years
preferred by company
Bangalore, India
1 May 14, 2026
Job Description
Job Type: Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes

Associate Scientist / Senior Research Associate – Translational Medicine (Genomics)

Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Department: BBRC / Translational Medicine / Genomics & Molecular Biology
Company: Syngene
Experience Required: 2–6+ Years (Relevant Wet Lab Genomics Experience Preferred)


Job Overview

An exciting scientific opportunity is available for an experienced Associate Scientist / Senior Research Associate within the translational medicine and genomics research domain. This role is ideal for professionals with strong expertise in NGS workflows, molecular biology, genomics assay development, biomarker analysis, translational research, and high-throughput molecular testing platforms.

The selected candidate will contribute to translational and clinical research programs involving genomics, transcriptomics, biomarker assay development, gene expression profiling, and molecular assay validation, supporting cutting-edge precision medicine and translational science initiatives.

This role is highly suited for professionals seeking advancement in genomics research, translational medicine, molecular diagnostics, biomarker development, and pharmaceutical R&D sciences.


Key Responsibilities

Genomics & Translational Research Execution

  • Design, optimize, evaluate, and execute genomics and transcriptomics workflows for translational and clinical research programs
  • Support assay implementation based on study requirements and capability development goals
  • Deliver high-quality scientific outputs aligned with project timelines and research objectives

NGS & Molecular Assay Development
Develop, optimize, validate, and execute assays including:

  • Next Generation Sequencing (NGS)
  • RNA Sequencing (RNA-Seq)
  • Whole Exome Sequencing (WES)
  • Whole Genome Sequencing (WGS)
  • qPCR assays
  • ddPCR assays
  • PCR workflows
  • Genotyping assays
  • Gene Expression Profiling (GEP)

Support assay qualification, troubleshooting, QC review, and execution excellence.

Sample Processing & Molecular Workflows
Work with biological sample types including:

  • FFPE tissue samples
  • Blood
  • Saliva
  • Liquid biopsy samples
  • Other biological fluids
  • Human and animal research samples

Perform workflows including:

  • DNA extraction
  • RNA extraction
  • Sample preparation
  • Library preparation
  • Molecular QC workflows

Biomarker & Clinical Research Support

  • Support biomarker assay platform selection and evaluation
  • Review in-house and vendor-generated genomics data
  • Contribute to translational medicine and clinical development biomarker programs
  • Support precision medicine research initiatives

Automation & High-Throughput Platform Support

  • Support qualification and validation of automated genomics workflows
  • Work with automated liquid handling systems for high-throughput genomics operations
  • Contribute to scalable workflow optimization for research programs

Cross-Functional Collaboration
Collaborate closely with:

  • Clinical operations
  • Sample management teams
  • Biorepository teams
  • Translational medicine scientists
  • External stakeholders
  • Cross-functional research teams

Ensure strong scientific coordination across research workflows.

Scientific Documentation & Quality Compliance
Prepare and maintain:

  • Scientific reports
  • SOPs
  • Experimental documentation
  • Validation records
  • QC documentation
  • Study execution records

Maintain accurate documentation within:

  • ELN systems
  • LIMS platforms

Ensure compliance with quality standards and established GCP-aligned documentation practices.

Project Management & Scientific Delivery

  • Manage multiple scientific programs simultaneously
  • Ensure timely completion of experiments and deliverables
  • Communicate findings effectively to internal stakeholders
  • Maintain data quality, reproducibility, and scientific rigor

Required Qualifications

Educational Qualifications
Candidates must hold:

  • M.Sc
  • M.Tech

Preferred specialization:

  • Biotechnology
  • Molecular Biology
  • Life Sciences
  • Genomics
  • Related biomedical sciences