Regulatory Coordinator

Novartis is hiring experienced Regulatory Affairs professionals for the position of Regulatory Coordinator at its Hyderabad office. This is a full-time opportunity for candidates who have experience in pharmaceutical regulatory operations and want to work on global regulatory projects supporting product registrations and lifecycle management.

Position Details

• Company: Novartis

• Job Title: Regulatory Coordinator

• Location: Hyderabad

• Employment Type: Full-Time

• Application Deadline: 7 August 2026

Role Summary

The Regulatory Coordinator supports regulatory activities throughout the product lifecycle, including new registrations, product variations, approvals, manufacturing transfers, and post-approval changes. The role involves coordinating with global regulatory teams, technical operations, quality functions, and regional stakeholders to help ensure regulatory activities are completed efficiently and in accordance with applicable requirements.

Key Responsibilities

• Coordinate the collection and availability of regulatory documents required for submissions and product maintenance.

• Work with internal and external stakeholders to support timely regulatory filings and approvals.

• Monitor project timelines and ensure regulatory deliverables are completed within agreed schedules.

• Participate in cross-functional project meetings and provide regulatory coordination support.

• Identify potential regulatory risks and assist in developing appropriate mitigation plans.

• Maintain compliance with internal procedures and applicable regulatory guidelines.

• Support communication and collaboration between global, regional, and local regulatory teams.

• Contribute to regulatory planning for product launches, manufacturing transfers, and lifecycle management activities.

Eligibility Criteria

Candidates should possess:

• At least 2 years of experience in Regulatory Affairs or a related pharmaceutical function.

• Strong communication and stakeholder management skills.

• Good analytical, organizational, and problem-solving abilities.

• Experience working in a collaborative, cross-functional environment.

• Ability to prioritize multiple activities and meet project deadlines.

• A proactive approach with a focus on quality and timely execution.

Preferred Skills

• Pharmaceutical Regulatory Affairs

• Regulatory Compliance

• Project Coordination

• Clinical Trial Awareness

• Cross-functional Collaboration

• Project Planning

• Attention to Detail

• Risk Management

Why Consider This Opportunity?

This position offers the opportunity to work on international regulatory projects while collaborating with global teams across multiple regions. It is well suited for Regulatory Affairs professionals seeking to expand their experience in product registrations, compliance, and lifecycle management within a leading pharmaceutical organization.

Last Date to Apply: 7 August 2026