Global pharma leader Novartis is hiring for two high-impact roles in Quality Operations and Clinical Development Fellowship in Hyderabad. These opportunities are ideal for candidates aiming to build careers in pharmaceutical quality assurance, GMP compliance, and clinical research development.
If you’re targeting roles in QA, QC, Regulatory Affairs, Clinical Trials, or Drug Development, this is a premium opportunity to work with a global innovator.
1. Specialist/Analyst โ Quality Operations (Hyderabad)
Key Responsibilities
- Ensure cGMP compliance and adherence to Novartis Quality Management System
- Support QC release activities (Inspection plans, COA, CoC, specifications)
- Author testing monographs & perform impact assessments
- Handle Nitrosamine risk assessment reports (Step 1 & Step 2)
- Perform statistical analysis, performance trending & business reporting
- Support audit readiness (internal & regulatory inspections)
- Ensure compliance with GxP, data integrity & regulatory standards
Qualifications
- B.Pharm / M.Pharm / MSc / Engineering / MBA
- Minimum 3+ years experience in QA / QC / Manufacturing
- Strong knowledge of GMP, QMS, Regulatory compliance
- Experience with global stakeholders & audit environments
Key Skills
- Quality Management System (QMS)
- GMP & Regulatory Compliance
- Risk Assessment (Nitrosamines)
- Analytical Methods
- Data Integrity & Digital Tools
Salary (Estimated)
โน6 LPA โ โน12 LPA (based on experience)
2. Clinical Development Fellow (2-Year Program)
Program Overview
A 2-year postgraduate fellowship designed to provide hands-on experience in clinical trials, protocol development, and global drug development.
Start Date: September 1, 2026
Location: Hyderabad
Key Responsibilities
- Develop clinical trial documents (CTP, ICF, CRF, CSR)
- Support clinical data review & medical analysis
- Prepare patient safety reports & regulatory submissions
- Contribute to clinical study reports & publications
- Participate in global clinical development programs
Therapeutic Areas
- Oncology
- Neuroscience & Gene Therapy
- Cardiovascular & Metabolism
- Immunology
- Global Health
Qualifications
- MD / PharmD / MSc (Life Sciences)
- Completed within last 2 years
- Strong interest in clinical development & trials
Skills Required
- Clinical Research & Trial Documentation
- Medical Writing & Data Analysis
- Communication & Stakeholder Management
- Problem Solving & Scientific Thinking
Stipend (Estimated)
โน8 LPA โ โน15 LPA (fellowship-based)
Why Join Novartis? (Benefits)
- Work with a top global pharmaceutical company
- Exposure to international clinical trials & regulatory frameworks
- Strong career growth in QA, Clinical Research, and Drug Development
- Opportunity to work with cutting-edge therapies & innovation
- Collaborative global team environment
Application Process
Application Link For Specialist/Analyst โ Quality Operations
Application Link For Clinical Development Fellow (2-Year Program)
