Novartis Hiring Global Regulatory Submission Manager in India | Regulatory Affairs Job 2026

Global Regulatory Submission Manager Job 2026

Novartis India | Regulatory Affairs Careers

📍 Hyderabad, India | Global R&D Hub | Job ID: REQ-10073777

A great career opportunity for experienced Life Science professionals in the pharmaceutical regulatory field! 🎉 Global giant Novartis is hiring for its development hub in Hyderabad. This role is ideal for experts in Regulatory Affairs, Drug Development, and Global Submissions.

📌 Job Overview

Company: Novartis India

Role: Global Submission Manager

Experience: 5+ Years Preferred

Location: 📍 Hyderabad

Business Unit: Development / R&D

Work Mode: Office-based

💼 Key Responsibilities

• Submission Management: Lead large and complex global regulatory submission projects.
• Strategy Support: Contribute to regulatory strategies for global product registration.
• Dossier Preparation: Coordinate the preparation of dossiers for FDA, EMA, and other health authorities.
• Controlled Documentation: Maintain records and manage technical abstracts, reports, and data analysis.

🎓 Educational Qualification & Experience

Education: Bachelor's or Master's degree in Life Sciences or a related discipline.

Experience: 3–5 years in Regulatory Affairs or Regulatory Submissions with knowledge of global drug development processes.

🧠 Required Skills

Global Submissions (eCTD) FDA & EMA Guidelines ICH Guidelines Project Management Cross-functional Collaboration

Join a world-class pharmaceutical leader. Apply now:

🚀 Apply via Novartis Career Portal

(Search using Job ID: REQ-10073777)

💡 Career Tip: Focus on mastering eCTD submission formats and Clinical Trial Regulations to accelerate your growth in Regulatory Affairs.

Novartis India | Discovering the Future of Medicine
📍 Hyderabad Development Center, Telangana