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Hiring Quality Analyst & Clinical Development Fellow
Novartis
Hyderabad
0–3 Years
Quality / Clinical Research
Pharma
🏢 About Novartis
Novartis is a global pharmaceutical leader focused on reimagining medicine through innovation, research, and advanced therapies. The company operates across multiple therapeutic areas and is known for cutting-edge drug development and global clinical trials.
Working at Novartis provides strong exposure to global regulatory frameworks, quality systems, and clinical research programs.
🧪 Role 1: Specialist / Analyst – Quality Operations
Location: Hyderabad
Key Responsibilities:
- Ensure compliance with cGMP and Quality Management Systems
- Support QC release activities (COA, specifications, inspection plans)
- Perform risk assessments (Nitrosamines)
- Handle audit readiness and regulatory inspections
- Perform data analysis, trending, and reporting
- Maintain compliance with GxP and data integrity standards
Eligibility:
- B.Pharm / M.Pharm / MSc / Engineering / MBA
- Experience: 0–3+ Years
- Knowledge of GMP, QMS, Regulatory Compliance
Salary: ₹6 – ₹12 LPA (Estimated)
🧬 Role 2: Clinical Development Fellow (2-Year Program)
Location: Hyderabad
Program Duration: 2 Years
Key Responsibilities:
- Develop clinical trial documents (Protocol, CRF, CSR)
- Perform clinical data review and analysis
- Prepare safety reports and regulatory submissions
- Support global clinical development programs
- Contribute to scientific publications
Therapeutic Areas:
- Oncology
- Neuroscience
- Cardiovascular
- Immunology
Eligibility:
- MD / PharmD / MSc (Life Sciences)
- Completed within last 2 years
- Strong interest in clinical research
Stipend: ₹8 – ₹15 LPA (Estimated)
⭐ Why Join Novartis?
- Global pharma exposure
- Work on advanced therapies and clinical trials
- Strong career growth in QA & Clinical Research
- Collaborative global work environment
- Learning & development opportunities
🎯 Interview Preparation Tips
- Revise GMP, GxP & Quality Systems
- Understand clinical trial phases & documentation
- Learn regulatory guidelines (ICH-GCP)
- Prepare basic pharma/clinical concepts
📌 Note Before You Apply:
Select the correct role before applying and ensure your eligibility matches the requirements.
Select the correct role before applying and ensure your eligibility matches the requirements.
👇 Select Role & Apply 👇
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