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Manager- International Regulatory Lead

Amgen
8-13 years
INR 28 LPA – 50 LPA
Hyderabad
1 June 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Regulatory Affairs, Regulatory Writing, Regulatory Compliance, Global Submissions, eCTD, IND/NDA/BLA Submissions, ICH-GCP, Regulatory Strategy, Regulatory Intelligence, Labeling Strategy.

MANAGER – INTERNATIONAL REGULATORY LEAD (IRL)

Location: Hyderabad, India
Work Type: On-Site
Job ID: R-242348
Department: Regulatory Affairs
Posted On: May 27, 2026


ABOUT AMGEN

Amgen is one of the world's leading biotechnology companies dedicated to discovering, developing, manufacturing, and delivering innovative medicines that help patients fight serious illnesses. Leveraging cutting-edge science, technology, and human genetics, Amgen has been at the forefront of biotechnology innovation for more than four decades, improving the lives of millions of patients worldwide.


POSITION SUMMARY

The International Regulatory Lead (IRL) Manager provides strategic regulatory leadership and expertise for one or more Amgen products across international markets. This role is responsible for developing and executing international regulatory strategies, supporting product registrations, managing lifecycle activities, and ensuring alignment between global, regional, and local regulatory requirements.

The incumbent will collaborate closely with cross-functional teams and country regulatory affiliates to optimize product development, accelerate approvals, maintain compliance, and support successful commercialization in international markets.


KEY RESPONSIBILITIES

Regulatory Strategy & Leadership

  • Develop and execute international regulatory strategies for assigned products.

  • Contribute to Global Regulatory Plans and product development strategies.

  • Provide regulatory guidance to global teams regarding international regulatory requirements and implications.

  • Identify regulatory opportunities, risks, and mitigation strategies.

  • Support regulatory compliance activities, including:

    • Regulatory Information Management (RIM)

    • Post-Marketing Commitments (PMCs)

    • Agency Commitments

    • ESC Levels


Regulatory Submission Management

  • Plan, coordinate, and support regulatory submissions including:

    • Clinical Trial Applications (CTAs)

    • Marketing Authorization Applications (MAAs)

    • Lifecycle Management Submissions

  • Prepare, review, and maintain regulatory documentation.

  • Author and redact documents supporting regulatory filings.

  • Support local regulatory teams in responding to health authority questions.

  • Ensure timely and compliant regulatory submissions across assigned international markets.


Product Labeling Strategy

  • Lead international product labeling activities.

  • Collaborate with Labeling Working Groups (LWG) and cross-functional teams.

  • Support alignment of local labels with:

    • Company Core Data Sheet (CCDS)

    • Reference Label

    • Regulatory Requirements

  • Manage label negotiations and deviation requests.

  • Ensure consistency and compliance of product labels across international markets.


Agency Interactions

  • Participate in planning and execution of regulatory agency meetings.

  • Lead internal discussions related to agency interactions.

  • Communicate regulatory outcomes and recommendations to Global Regulatory Teams.

  • Support local affiliates during agency engagements and regulatory negotiations.


Regulatory Intelligence & Research

  • Monitor evolving regulatory regulations, guidelines, and industry trends.

  • Conduct regulatory intelligence research and analysis.

  • Identify precedents, submission histories, and regulatory pathways to support product advancement.

  • Provide strategic recommendations based on regulatory intelligence findings.


Cross-Functional Collaboration

  • Serve as an active member of:

    • Global Regulatory Teams (GRT)

    • Clinical Study Teams (CST)

    • Evidence Generation Teams (EGT)

    • Labeling Working Groups (LWG)

  • Collaborate with:

    • Clinical Development

    • Medical Affairs

    • Commercial Teams

    • Manufacturing

    • Quality Assurance

    • Local Regulatory Affiliates

  • Build strong partnerships across global and regional functions.


Process Improvement & Operational Excellence

  • Support regulatory process improvement initiatives.

  • Drive operational efficiencies and best practices.

  • Contribute to performance metrics and compliance programs.

  • Promote continuous improvement within regulatory operations.


REQUIRED KNOWLEDGE & TECHNICAL SKILLS

Regulatory Expertise

  • Strong understanding of global regulatory frameworks.

  • Knowledge of medicinal product legislation and regulations.

  • Experience with:

    • Clinical Trial Applications (CTA)

    • Marketing Authorizations (MA)

    • Product Registrations

    • Lifecycle Management

    • Regulatory Compliance


Drug Development Knowledge

  • Understanding of pharmaceutical and biotechnology product development.

  • Knowledge of clinical development processes.

  • Familiarity with global registration procedures and regulatory pathways.

  • Awareness of expedited approval mechanisms and special regulatory designations.


International Regulatory Knowledge

Experience and understanding of:

  • Orphan Drug Designation

  • Pediatric Investigation Plans

  • Compassionate Use Programs

  • Expedited Regulatory Pathways

  • International Registration Procedures

  • Post-Approval Regulatory Activities


CORE COMPETENCIES

Leadership & Strategic Thinking

  • Regulatory strategy development

  • Risk assessment and mitigation

  • Decision-making capability

  • Project leadership

Communication & Influencing Skills

  • Excellent verbal communication

  • Strong written communication

  • Presentation skills

  • Negotiation and influencing abilities

Collaboration & Relationship Management

  • Cross-functional teamwork

  • Stakeholder management

  • Global collaboration

  • Relationship building

Problem Solving & Analytical Skills

  • Conflict resolution

  • Critical thinking

  • Regulatory issue management

  • Data interpretation and decision support

Cultural Agility

  • Ability to work effectively across international markets

  • Strong cultural awareness and sensitivity

  • Experience collaborating with global teams


EDUCATION & EXPERIENCE

Minimum Qualifications

Option 1

Doctorate Degree (PhD, PharmD, MD or equivalent)

  • Minimum 6 years of directly related regulatory experience

Option 2

Master’s Degree

  • Minimum 8 years of directly related regulatory experience

Option 3

Bachelor’s Degree

  • Minimum 10 years of directly related regulatory experience


Preferred Qualifications

  • 8–13 years of Regulatory Affairs experience.

  • Significant international regulatory experience.

  • Strong understanding of regional and international regulatory requirements.

  • Experience supporting product development and global registrations.

  • Biotechnology and/or pharmaceutical industry experience.