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Senior Manager – Regulatory Affairs (Cmc) – Us Market

Sun Pharma
Sun Pharma
10-15 years
preferred by company
Gurgaon, India
1 May 14, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, mRS and EQ-5D-5L., Narrative Writing

Senior Manager – Regulatory Affairs (CMC) – US Market

Location: Gurgaon, Haryana, India
Employment Type: Full-Time
Department: Clinical Development / Regulatory Affairs / CMC Regulatory Affairs
Experience Required: 10–15 Years
Education Required: M.Pharm (Pharmaceutical Sciences)


Job Overview

A senior strategic opportunity is available for an experienced Senior Manager – Regulatory Affairs (CMC) – US Market within the global pharmaceutical regulatory affairs domain. This role is ideal for seasoned professionals with expertise in CMC regulatory strategy, NDA submissions, IND/CTA documentation, lifecycle management, US FDA regulatory compliance, global market approvals, and cross-functional regulatory leadership.

The selected candidate will serve as the CMC Regulatory Product Lead, driving end-to-end Chemistry, Manufacturing, and Controls (CMC) regulatory strategy for branded pharmaceutical products targeted for the US market, while also supporting advanced regulated markets including Europe and Canada.

This role is highly suited for professionals seeking advancement in global regulatory affairs leadership, CMC strategy, pharmaceutical product approvals, lifecycle management, and regulatory compliance governance.


Key Responsibilities

CMC Regulatory Strategy Leadership

  • Serve as the primary CMC Regulatory Product Lead for assigned branded pharmaceutical products
  • Define and drive global CMC regulatory strategy for development and commercialization programs
  • Lead regulatory planning for product approvals across:
    • United States
    • Europe
    • Canada
    • Other advanced regulated markets
  • Assess regulatory risk, approval probability, and mitigation strategies for complex development programs

Regulatory Submission Management
Lead preparation, review, and execution of CMC regulatory submissions including:

  • PIND submissions
  • IND applications
  • CTA submissions
  • Original NDA filings
  • Marketing Authorization Applications (MAA)
  • Annual reports
  • Post-approval supplements
  • Regulatory variation submissions
  • Health authority response documentation

Ensure timely regulatory milestone delivery to support product continuity and approvals.

Product Lifecycle Management

  • Drive regulatory lifecycle management for approved products
  • Ensure timely submission of:
    • Annual reports
    • Labeling or manufacturing updates
    • Supplements
    • Regulatory amendments
    • Post-approval change documentation
  • Support uninterrupted market supply through proactive regulatory execution

Health Authority Interaction

  • Support communication and regulatory engagement with:
    • US FDA
    • EMA
    • Health Canada
    • Other international regulatory agencies
  • Prepare agency briefing packages and response documentation
  • Manage regulatory query resolution and agency interaction strategy

Cross-Functional Regulatory Leadership
Collaborate closely with:

  • Research & Development
  • CMC teams
  • Manufacturing
  • Analytical Development
  • Quality Assurance
  • Supply Chain
  • Clinical Development
  • Commercial stakeholders
  • External partners

Provide regulatory leadership across cross-functional development teams.

Due Diligence & Strategic Business Support

  • Support:
    • Product in-licensing evaluations
    • Due diligence regulatory assessments
    • Product divestment activities
    • Product withdrawal regulatory planning
  • Evaluate regulatory pathways and commercialization feasibility

Technical Dossier Development

  • Lead preparation and critical review of:
    • CMC dossiers
    • Technical documentation
    • Scientific justifications
    • Regulatory responses
    • Submission modules

Ensure clarity, scientific robustness, and compliance of regulatory documentation.

Innovation & Continuous Improvement

  • Support adoption of new technologies and modernization initiatives
  • Drive innovation in regulatory execution strategies
  • Improve CMC submission workflows and regulatory processes

Team Leadership & Mentorship

  • Mentor junior regulatory team members
  • Provide technical leadership across regulatory initiatives
  • Support team capability development and regulatory excellence

Required Qualifications

Educational Qualifications
Candidates must hold:

  • Master of Pharmacy (M.Pharm) in Pharmaceutical Sciences