Expert Science & Technology | Novartis
Company: Novartis Careers
Position: Expert Science & Technology
Job ID: REQ-10076531
Location: Hyderabad (Genome Valley)
Division: Development
Business Unit: Technical Research & Development (TRD)
Employment Type: Regular | Full-Time
Posted On: April 27, 2026
Role Overview
This role sits within Novartis Technical Research & Development (TRD) and focuses on analytical science supporting advanced biologics, especially:
Oligonucleotide therapeutics
Peptide-based therapeutics
The position bridges:
Analytical chemistry
Method development
Clinical performance evaluation
The ultimate goal is to support transformation of drug candidates into safe and effective medicines.
Key Responsibilities
1. Analytical Method Development & Validation
Responsible for:
Designing and validating analytical methods
Performing method feasibility studies
Supporting method transfers and stability testing
Conducting release testing and formulation analytics
Strong focus on:
Robust, regulatory-compliant analytical methodologies
2. Chromatography & Mass Spectrometry Analysis
Core technical expertise required in:
Liquid chromatography techniques:
Reverse-phase (RP)
Ion-exchange (IEX)
HILIC
Also desirable:
Mass spectrometry for biological molecules
Mass confirmation
Impurity profiling
Sequencing analysis
Quantitative analysis
3. Experimental Planning & Execution
Responsible for:
Planning and conducting scientific experiments
Executing analytical development workflows
Maintaining documentation aligned with timelines and quality standards
Experiments include:
Method development and validation
Stability studies
Analytical transfers
Release testing support
4. Data Management & Documentation
Ensure:
Accurate entry of laboratory data into LIMS systems
Proper test activation and result documentation
Strict adherence to Good Documentation Practices (GDP)
Compliance with Good Laboratory Practices (GLP)
5. Quality, Compliance & Regulatory Standards
Responsible for:
Maintaining GMP compliance in all laboratory activities
Ensuring regulatory readiness of analytical data
Supporting internal and external audits
Preventing critical audit findings within scope
6. Data Analysis & Investigation
Support scientific interpretation of results:
Investigate OOS (Out-of-Specification) results
Handle deviations and change controls
Resolve system suitability test (SST) failures
Support root cause analysis
7. Laboratory Operations & Management
Oversee assigned lab activities:
Chemicals and reagent management
Sample handling and storage
Column and consumables management
Glassware and equipment upkeep
Promote:
Lean lab practices
Efficiency improvements
Environmentally sustainable operations
8. Cross-Functional Communication
Responsible for:
Communicating critical issues promptly
Collaborating with project teams
Supporting decision-making with analytical insights
Participating in scientific discussions
Required Qualifications
Education
One of the following:
PhD in Analytical Chemistry (or equivalent) with 1–3 years experience
OR
M.Pharm / M.Sc. with 8+ years experience in pharmaceutical analytical development
Experience
Must have:
Strong experience in pharmaceutical analytical development
Hands-on expertise in oligonucleotide or peptide analytics
Experience in GMP-regulated environments
Technical Skills
Essential:
Liquid chromatography (RP, IEX, HILIC)
Analytical method development and validation
GMP/GLP compliance
Laboratory data systems (LIMS)
Desirable:
Mass spectrometry (biologics analysis, sequencing, impurity profiling)
Chromatography software (e.g., Chromeleon)
Regulatory & Quality Knowledge
Must understand:
GMP requirements
Regulatory expectations for analytical data
Pharmaceutical quality systems
Audit readiness practices
Soft Skills
Strong abilities in:
Scientific communication (written and verbal)
Data interpretation and problem-solving
Time management and prioritization
Cross-functional collaboration
Attention to detail
Documentation discipline
Tools & Systems
Expected familiarity with:
Microsoft Office Suite
LIMS systems
Chromatography data analysis software
Laboratory workflow tools
What Novartis Looks For
Ideal candidates demonstrate:
Deep expertise in analytical chemistry for biologics
Strong chromatography and separation science background
GMP-compliant scientific rigor
Ability to work in regulated pharmaceutical environments
Strong ownership of experimental execution and data quality
Why Join Novartis?
This role enables you to:
Work on cutting-edge oligonucleotide and peptide therapeutics
Contribute directly to drug development success
Operate in a globally regulated R&D environment
Bridge analytical science with real clinical impact
Be part of innovative technical research teams in Genome Valley
Helpful Links
Careers
People & Culture
Benefits & Rewards
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