Job Description

Job Overview :


We are seeking a highly motivated Research Associate / Scientist to join our Cell and Gene Therapy (CGT) Projects . The role involves hands-on research in immune cell engineering , process development , and functional characterization of engineered cells , while working closely with cross-functional teams including Preclinical, GMP Manufacturing, Quality, and Regulatory Affairs .


This is an exciting opportunity to contribute to cutting-edge immuno-oncology and Build a good Career into CGT Domain & translational research programs.


Suitable Profiles :

  • PhD / M.Sc. / M.Tech in Life Sciences, Biotechnology, Biochemistry, Biology, or related disciplines
  • 2-5 years of relevant research experience
  • Strong foundation in Immunology, Cell Biology, and Molecular Biology



Roles and Responsibilities

  • Design, plan, and perform laboratory experiments related to various immune cell engineering and the development of robust manufacturing processes for cell therapy products.
  • Manage and execute immune cell culture and differentiation, including primary cell culture, cell line maintenance, and gene modification techniques (e.g., using lentiviral vectors, CRISPR-Cas9 systems, etc.).
  • Prior experience in generation of lentiviral vectors, viral infection of primary cells and advanced molecular biology techniques, including gene editing techniques will be preferred.
  • Develop and perform a variety of cellular and molecular assays for the functional characterization and phenotyping of the engineered cells, using flow cytometry, ELISA, qPCR, ddPCR, live-cell imaging, metabolic health assessments and co-culture set-ups for cytotoxicity testing.
  • Accurately collect, record, analyze, and interpret experimental data. Use statistical analysis (e.g., Design of Experiments/DoE) to determine critical process parameters.
  • Be able to troubleshoot experiments, analyse data and interpret scientific presentations.
  • Ensure all research activities comply with regulatory requirements.
  • Identify, analyze, and resolve technical issues during research and process development, implementing process improvements.
  • Present research findings, project progress, and scientific strategy to stakeholders, potentially including external collaborators or conferences.
  • Involve in projecting requirements, interacting with vendors, and engaging in the pipeline of procuring new consumables and equipment required for the project.
  • Work closely within highly matrixed, cross-functional teams and mentor junior scientists or research associates to advance company's Cell and Gene therapy pipeline.
  • Communicate effectively to interface with internal functional departments to support the workflow of various study-related activities.
  • Coordinate with Preclinical, GMP manufacturing, Quality control, Quality assurance and supply chain teams and strictly adhere to project timelines by preserving integrity, accuracy, safety and quality.
  • Actively engage in non-GMP validation and IND filing studies.
  • Prepare and involve in compliance monitoring inspections and regulatory agency interactions.

Understand systems and process pertaining to sterile practices, work ethics, safety, health and environment.


Competencies

  • PhD / M.Sc. / M.Tech in Biology, Biotechnology, Biochemistry , or related fields
  • Coursework in Cell Biology, Immunology, Molecular Biology
  • Strong expertise in T-cell or NK-cell biology , immuno-oncology, and CGT processes
  • Hands-on experience in:
  • Aseptic processing
  • Flow cytometry
  • Live-cell imaging
  • qPCR / ddPCR
  • Viral transduction
  • Molecular biology techniques
  • Problem Solving
  • Excellent analytical and critical thinking skills to resolve complex scientific and process-related challenges
  • Strong written and verbal communication skills
  • High attention to detail and organizational abilities
  • Ability to work efficiently in a fast-paced, collaborative environment
  • Strong documentation and record-keeping skills in line with regulatory and quality standards

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