Great opportunity as Research Associate, Scientist at Stelis Biopharma

Website Stelis Biopharma

As a fully integrated pure-play biologics Contract Development and Manufacturing Organization (CDMO), we offer a comprehensive range of services to support the development and production of biologic drugs. Your capabilities span from cell line technology transfer to clinical and commercial manufacturing, including the ability to convert drug substances into stable formulations and provide fill and finish services.

Our technical expertise covers various technology platforms, such as microbial, mammalian, and viral vectors, which are essential for producing a diverse range of biologics. Additionally, our world-class cGMP manufacturing facilities ensure that we can maintain high-quality standards throughout the production process.

Job Opportunity: Research Associate / Sr. Research Associate / Scientist – Analytical Development Department, Unit-1

Job Requirements / Qualifications:


  • Master’s degree in Biotechnology / Biochemistry / Molecular Biology / Life Sciences from Tier-1 or Tier-2 institutes of India, with a strong commitment to building a successful career in the field of biological research.
  • Demonstrated experience in scientific writing, experimental design, data review, and regulatory documentation within a Quality Management System (QMS) framework.


  • Willingness to work across different unit locations within the organization and a readiness to travel (inter / intra city) for training and technology transfers, as required.
  • Soft skills such as effective communication, attention to detail, time management, collaboration & interpersonal skills, adaptability, and a problem-solving attitude.


  • 2-8 years of experience in the following domain areas:
    • Binding kinetics studies.
    • Non-cell-based platform assays.
    • Functional assays like Phosphorylation assays, AlphaLISA, FRET, and other advanced platforms.
    • qPCR-based techniques.
    • Data analysis.

Characterization Assays:

  • 2 to 8 years of experience with hands-on expertise in characterization.
  • Intact & submit mass identification, Peptide mapping, N-terminal sequencing.
  • Post-translational modifications (PTMs), disulfide linkages, and other workflows using UHPLC, HRMS, and related tools.
  • Understanding and interpretation of FTIR, CD Spectroscopy, CE-SDS.

Physiochemical Assays:

  • 2 to 8 years of experience in:
    • CE-SDS, iCEF, CZE.
    • Chromatographic techniques such as HIC, SE-HPLC, IEX, and newer platforms.

In-process, Stability, and Release Assays:

  • 2 to 8 years of experience in assays including, but not limited to:
    • RP-HPLC, HIC, SE-HPLC, IEX, and impurity clearance studies specifically applicable for process development, scale-up, and technology transfer to the quality control department.
    • Validation studies.
    • Technology transfer to QC.

Job Location: Bengaluru

Application Instructions: Interested and qualified candidates are encouraged to share their CVs to the following email address:

Last Date for Applications: 5th August, 2023

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