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Global Regulatory Submission Manager

Novartis
3-5 years
Not Disclosed
Hyderabad
10 May 20, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Company: Novartis
Novartis Official Website
Location: Hyderabad (Office)
Employment Type: Full-time
Requisition ID: REQ-10078004
Application Deadline: May 27, 2026


1. Role Overview

The Global Regulatory Submission Manager is responsible for coordinating, planning, and delivering worldwide regulatory submissions in compliance with global health authority requirements.

The role ensures accurate, timely, and compliant preparation of regulatory dossiers across multiple submission types and regions, supporting global drug development and product approvals.


2. Core Responsibilities

A. Regulatory Submission Planning & Execution

  • Lead cross-functional teams for global regulatory submission planning and execution

  • Manage multiple simultaneous submissions in formats such as:

    • eCTD (Electronic Common Technical Document)

    • NDA / BLA / IND submissions

    • MAA (CP, MRP, DCP)

    • Health Authority questions and compliance submissions

  • Anticipate technical and operational challenges and implement solutions


B. Submission Strategy & Guidance

  • Provide guidance on:

    • Submission structure and formatting requirements

    • Filing strategy across global regions

    • eCTD lifecycle management

    • Document compilation workflows

  • Ensure alignment with global regulatory standards and health authority expectations


C. Document Control & Publishing Coordination

  • Track and ensure timely delivery of submission components

  • Coordinate publishing activities with internal publishing teams

  • Manage internal review cycles and approval workflows

  • Maintain controlled documentation systems and record retention processes


D. Quality, Compliance & Troubleshooting

  • Ensure compliance with global regulatory requirements (FDA, EMA, ICH)

  • Troubleshoot technical and quality issues in submission compilation and dispatch

  • Maintain documentation integrity and audit readiness

  • Enforce formatting, procedural, and regulatory standards


E. Cross-Functional Collaboration & Efficiency

  • Collaborate with regulatory, clinical, CMC, safety, and publishing teams

  • Identify resource needs and implement process improvements

  • Contribute to operational excellence initiatives across regulatory functions


3. Required Qualifications

Education

  • Bachelor’s degree in Life Sciences or related field with 5+ years of experience

  • Preferred: Master’s degree in a relevant discipline


Experience

  • 3–5 years in Regulatory Affairs or regulatory submission-related roles

  • Experience with global regulatory submission publishing and eCTD systems

  • Familiarity with drug development lifecycle


Regulatory Knowledge

  • FDA regulations

  • EMA guidelines

  • ICH guidelines and global submission standards


4. Core Skills

Technical & Regulatory Skills

  • Regulatory submission publishing (eCTD / non-eCTD)

  • Documentation management and lifecycle control

  • Regulatory compliance and health authority submissions

  • Data extraction and analysis for regulatory content


Project & Operational Skills

  • Project management of multiple parallel submissions

  • Time and workflow management

  • Process coordination across global teams

  • Troubleshooting submission and publishing issues


Behavioral Skills

  • Strong communication (written and verbal)

  • Cross-functional collaboration

  • Independent working capability

  • Attention to detail and compliance mindset


5. Key Skill Areas (From JD Keywords)

  • Regulatory Compliance & Affairs

  • Documentation Management Systems

  • Lifesciences & Drug Development

  • Data Analysis for regulatory documentation

  • Waterfall-style project execution


6. Organizational Context

This role sits within global Regulatory Affairs and ensures that all regulatory submissions are accurately compiled, validated, and submitted to health authorities worldwide, enabling timely drug approvals and lifecycle management.