💼 Sandoz Careers 2025 | Regulatory Affairs Senior Specialist – Documentation
🏢 Company: Sandoz
📌 Role: Regulatory Affairs Senior Specialist – Documentation
🆔 Job ID: REQ-10024332
📍 Location: Telangana, India
🧪 Function: Research & Development
🕘 Shift: Day Shift
📄 Type: Full-time | Regular
📝 Key Responsibilities:
📌 CMC & Module 3 documentation
📌 DMF preparation & global submissions
📌 ICH Q11, ICH M7 & regulatory compliance
📌 Health authority submissions & query responses
📌 Lifecycle management & CMC change assessment
📌 SOPs, regulatory guidance & cross-functional coordination
🎓 Required Skills:
✅ Strong scientific & technical writing
✅ Module 3 (CMC) documentation knowledge
✅ Global regulatory guideline understanding
✅ MS Word & Excel proficiency
✅ SOP compliance & independent working ability
🌍 Why Sandoz:
💊 Global leader in generics & biosimilars
👥 Impact ~500 million patients annually
📈 Global regulatory exposure
🤝 Collaborative culture & strong career growth
👉 Apply Here: Application Link
