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Expert Science & Technology

Novartis
Novartis
1-8 years
preferred by company
10 Jan. 19, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Expert – Science & Technology (Analytical R&D)

Job ID: REQ-10069212
Location: Hyderabad, India (Genome Valley)
Employment Type: Full-time | Regular
Function: Research & Development – Analytical Science
Business Unit: Global Drug Development (GDD)
Posted On: January 14, 2026


About the Organization

Novartis Global Analytical Research & Development is a high-impact, science-driven organization with over 400 analytical scientists across four countries, focused on delivering innovative, patient-centric medicines. Operating within the Technical Research and Development (TRD) organization, this team plays a critical role in bridging analytical science with clinical performance to transform molecules into life-changing therapies.

The role is based at Genome Valley, Hyderabad, a key global R&D hub for Novartis.


Role Overview

Novartis is seeking an Expert – Science & Technology to support analytical development for innovative oligonucleotide and peptide therapeutics. This position focuses on developing, validating, and transferring robust analytical methodologies while ensuring compliance with global quality and regulatory standards.

The role requires deep expertise in chromatographic techniques, with additional exposure to mass spectrometry and strong experience in analytical method development within a regulated pharmaceutical environment.


Key Responsibilities

  • Design, develop, validate, and transfer analytical methods for oligonucleotide and peptide-based therapeutics

  • Perform analytical feasibility studies and establish robust, compliant methodologies

  • Plan, execute, and document analytical experiments including method development, validation, stability, release testing, and formulation analytics

  • Ensure accurate documentation and timely submission of raw data using systems such as LIMS

  • Adhere to Good Documentation Practices (GDP), Good Laboratory Practices (GLP), and GMP standards

  • Investigate and evaluate deviations, OOX results, SST failures, and change controls

  • Manage laboratory-related activities including reagents, consumables, samples, columns, and equipment

  • Implement lean, efficient, and environmentally sustainable laboratory practices

  • Support internal and external audits with no critical observations within assigned scope

  • Communicate technical issues, risks, and progress proactively to project stakeholders

  • Contribute to Key Quality Indicators (KQI) and Key Performance Indicators (KPI) targets

  • Mentor colleagues and contribute to scientific knowledge-sharing initiatives


Required Qualifications & Experience

  • Ph.D. in Analytical Chemistry or related discipline with 1–3 years of pharmaceutical industry experience,
    OR

  • M.Pharm / M.Sc. with a minimum of 8 years of experience in analytical development within the pharmaceutical industry

  • Strong hands-on experience in oligonucleotide and peptide analytical development

  • Mandatory expertise in liquid chromatography techniques, including RP, IEX, and HILIC

  • GMP experience is mandatory, with strong understanding of quality systems and compliance requirements


Preferred Skills & Competencies

  • Experience with mass spectrometry, including impurity profiling, quantitation, and sequencing

  • Proficiency in chromatography data systems and analytical software (e.g., Chromeleon, LIMS)

  • Strong understanding of regulatory expectations and quality principles in drug development

  • Proven ability to guide, mentor, and technically support team members

  • Experience contributing to scientific forums and cross-functional knowledge exchange

  • Strong scientific writing, presentation, and communication skills

  • Ability to work independently while collaborating within a global, matrixed environment


Why Join Novartis

At Novartis, advancing healthcare requires more than innovation—it requires collaboration, purpose, and passion. You will be part of a global scientific community committed to improving patient outcomes and shaping the future of medicine through excellence in science and technology.


Benefits & Rewards

Novartis offers competitive compensation and comprehensive benefits designed to support personal and professional growth. Details are available through the company’s global benefits framework.


Job Details

  • Division: Development

  • Functional Area: Research & Development

  • Work Location: Hyderabad (Office-based)

  • Shift Work: No