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Clinical Label Management Analyst Job
Novartis
Hyderabad
2–3 Years
Clinical Trial Supply
GMP & IMP Labeling
Hybrid
🏢 About Novartis
Novartis is a global healthcare leader committed to reimagining medicine through innovation, regulatory excellence, and high-quality clinical supply operations supporting global clinical trials.
📌 Job Overview
- Role: Analyst – Clinical Label Management
- Location: Hyderabad
- Experience Required: 2–3 Years
- Work Model: Hybrid
- Domain: Clinical Trial Supply & Labeling Operations
- Last Date to Apply: 28 February 2026
🔬 Key Responsibilities
- Design and generate IMP labels as per study requirements
- Manage randomization lists & labeling schedules
- Ensure GMP & Health Authority compliance
- Maintain Phrase Library & label templates
- Upload study label templates & documentation
- Perform GMP Line Unit Checks (if certified)
- Report deviations & quality events
- Coordinate with supply chain & label vendors
- Support audits & regulatory inspections
- Provide status updates to Label Lead
🎓 Education & Qualifications
- BSc / MSc (Life Sciences, Chemistry, Biotechnology)
- B.Pharm / M.Pharm or equivalent scientific degree
- Experience in pharmaceutical manufacturing or clinical supply
🧪 Required Skills
- Knowledge of GMP & clinical trial labeling processes
- Experience with SAP ERP & supply chain systems
- Understanding of Health Authority compliance
- Project coordination & planning skills
- Strong documentation & communication skills
- Ability to work in global cross-functional teams
💼 Benefits of Working at Novartis
- Competitive salary & performance benefits
- Exposure to global clinical trials
- Strong compliance & innovation culture
- Career growth in clinical operations & supply chain
- Collaborative hybrid work environment
📌 Note Before You Apply:
Candidates with clinical supply, GMP labeling, or IMP packaging experience will have a strong advantage.
Candidates with clinical supply, GMP labeling, or IMP packaging experience will have a strong advantage.
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