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Expert Science &Technology

Novartis
Novartis
1-3 years
Not Disclosed
Hyderabad
1 May 6, 2026
Job Description
Job Type: Full Time Education: PhD in: Analytical Chemistry Pharmaceutical Sciences Biotechnology Chemistry Skills: Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat

Expert Science & Technology

Location: Hyderabad (Office)
Job Type: Full-Time
Experience Required: 1–3 Years (PhD Candidates) or 8+ Years (M.Pharm/M.Sc. Candidates)
Application Deadline: May 11, 2026
Industry: Pharmaceutical / Biotechnology / Analytical Research & Development


Job Overview

We are seeking a highly motivated and technically skilled Expert Science & Technology professional to support analytical development activities for innovative oligonucleotide and peptide therapeutics within a cutting-edge pharmaceutical R&D environment. This role involves designing, planning, executing, and documenting scientific studies that contribute to transforming advanced molecules into life-changing medicines.

The selected candidate will work within the Technical Research & Development (TRD) organization at Genome Valley, Hyderabad, and contribute to analytical science, laboratory operations, quality compliance, and process optimization activities.


Key Responsibilities

Analytical Development & Scientific Research

  • Perform method feasibility studies and validate robust analytical methodologies for:
    • Oligonucleotide therapeutics
    • Peptide therapeutics
  • Plan, organize, execute, and document scientific experiments related to:
    • Analytical Method Development
    • Method Validation
    • Method Transfer
    • Stability Testing
    • Release Testing
    • Formulation Development Analytics
  • Ensure experiments are completed within approved timelines and quality standards.

Chromatography & Analytical Techniques

  • Apply advanced liquid chromatography separation techniques including:
    • Reverse Phase Chromatography (RP)
    • Ion Exchange Chromatography (IEX)
    • Hydrophilic Interaction Liquid Chromatography (HILIC)
  • Utilize analytical instrumentation and software for scientific evaluations and data interpretation.
  • Support analytical characterization using mass spectrometry techniques when applicable.

Laboratory Operations & Documentation

  • Ensure proper documentation and submission of raw analytical data using systems such as:
    • LIMS
    • Chromatography Data Systems
  • Maintain compliance with:
    • Good Documentation Practices (GDP)
    • Good Laboratory Practices (GLP)
    • GMP standards
  • Manage laboratory-related activities including:
    • Chemicals and reagents
    • Consumables and samples
    • Column management
    • Glassware handling
  • Promote efficient, sustainable, and lean laboratory practices.

Quality, Compliance & Investigations

  • Support investigations related to:
    • SST failures
    • OOX results
    • Deviations
    • Change controls
  • Ensure achievement of:
    • Key Quality Indicators (KQI)
    • Key Performance Indicators (KPI)
  • Participate in internal and external audits and maintain compliance readiness.

Communication & Collaboration

  • Communicate critical scientific findings, operational issues, and project updates proactively to managers and project teams.
  • Collaborate with analytical scientists, laboratory teams, and cross-functional stakeholders to support research and development activities.
  • Contribute to technical discussions, scientific problem-solving, and continuous improvement initiatives.

Required Qualifications

Educational Qualifications

Candidates must possess one of the following qualifications:

PhD Qualification Path

  • PhD in:
    • Analytical Chemistry
    • Pharmaceutical Sciences
    • Biotechnology
    • Chemistry
    • Or equivalent scientific discipline
  • Minimum 1–3 years of relevant pharmaceutical analytical development experience

Master’s Qualification Path

  • M.Pharm or M.Sc. with minimum 8+ years of pharmaceutical analytical development experience

Preferred Qualifications

  • Expertise in:
    • Oligonucleotide Analytics
    • Peptide Analytics
    • Pharmaceutical Analytical Development
  • Additional exposure to:
    • Mass Spectrometry
    • Method Validation
    • GMP/GLP regulated environments
  • Certifications in:
    • GMP
    • GLP
    • Laboratory Quality Systems
    • Pharmaceutical Compliance