Looking for Regulatory Affairs jobs in Hyderabad? Novartis is hiring a Regulatory Coordinator for its Hyderabad office. This is an excellent opportunity for pharmaceutical professionals with 2+ years of Regulatory Affairs experience who want to build a career with one of the world’s leading pharmaceutical companies.
The Regulatory Coordinator will support global regulatory operations, lifecycle management activities, marketing authorization submissions, production transfer projects, and regulatory compliance while collaborating with cross-functional global teams.
If you have experience in Regulatory Affairs, CMC coordination, regulatory documentation, and global submission support, this Novartis Regulatory Coordinator Job 2026 could be your next career move.
Job Details
| Particular | Details |
|---|---|
| Company | Novartis |
| Position | Regulatory Coordinator |
| Department | Regulatory Affairs |
| Job Type | Full Time |
| Location | Hyderabad, India |
| Experience | Minimum 2 Years |
| Qualification | B.Pharm, M.Pharm, M.Sc, Life Sciences or related pharmaceutical qualification |
| Apply Before | 07 August 2026 |
Key Responsibilities
The selected candidate will:
- Coordinate regulatory activities supporting product registrations and lifecycle management.
- Ensure timely procurement of regulatory documents including CPP, GMP Certificates, CoAs, registration samples, and other submission documents.
- Collaborate with Regulatory CMC, Technical Operations, Quality Assurance, Global Labelling, Supply Chain, and regional regulatory teams.
- Coordinate regulatory readiness for submissions across multiple global markets.
- Act as the Regulatory Affairs representative in project governance meetings.
- Monitor regulatory timelines, dossier preparation, approvals, and submission milestones.
- Identify regulatory risks and develop mitigation strategies.
- Ensure compliance with global and country-specific regulatory requirements.
- Support regulatory intelligence, knowledge sharing, and stakeholder communication.
Eligibility Criteria
Candidates should possess:
- B.Pharm
- M.Pharm
- M.Sc (Life Sciences)
- Other relevant Pharmaceutical or Life Sciences qualification
Experience Required
- Minimum 2 years of experience in Regulatory Affairs or related pharmaceutical functions.
Desired Skills
Candidates with the following skills will be preferred:
- Regulatory Affairs
- Regulatory Compliance
- Clinical Trial knowledge
- Project Planning
- Documentation Management
- Global Submission Coordination
- Cross-functional Collaboration
- Stakeholder Management
- Communication Skills
- Problem Solving
- Attention to Detail
- Time Management
Why Join Novartis?
Working at Novartis offers:
- Opportunity to work on global Regulatory Affairs projects.
- Exposure to international regulatory agencies.
- Cross-functional collaboration with global teams.
- Career growth in Regulatory Affairs and CMC operations.
- Inclusive and innovation-driven work culture.
- Learning opportunities within a leading multinational pharmaceutical company.
How to Apply
