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Manager - International Regulatory Lead

Amgen
Amgen
8-12 years
₹35 LPA – ₹65 LPA
Hyderabad
10 March 16, 2026
Job Description
Job Type: Full Time Education: PhD/B.Sc./M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Manager – International Regulatory Lead

Company: Amgen
Location: Hyderabad, Telangana, India
Job Type: Full-Time | On-Site
Experience: 8 – 12+ Years (Regulatory Affairs – Biotech / Pharma)
Qualification: Bachelor’s / Master’s / PhD in Life Sciences, Pharmacy, Biotechnology, or related field
Approx Salary: ₹35 LPA – ₹65 LPA


Job Overview

Amgen is seeking a Manager – International Regulatory Lead (IRL) to provide regulatory leadership for global product development and regulatory approvals across international markets.

This role will focus on developing regulatory strategies, managing global submissions, and coordinating with regional regulatory teams to support product registration and lifecycle management for Amgen’s therapies.

The position works closely with global regulatory teams, clinical development teams, and local regulatory authorities to ensure successful regulatory outcomes.


Key Responsibilities

1. Regulatory Strategy Development

  • Provide regulatory expertise to support global clinical development and marketing authorization strategies.

  • Develop international regulatory strategies and submission plans for product approvals.

  • Identify regulatory risks and develop contingency strategies for potential regulatory outcomes.


2. Regulatory Submissions & Documentation

  • Plan and manage clinical trial applications and marketing authorization submissions.

  • Prepare and maintain regulatory documentation supporting submissions.

  • Support labeling strategy development and submission activities.


3. Cross-Functional Collaboration

  • Work with Global Regulatory Teams (GRT) and cross-functional stakeholders.

  • Coordinate with regional regulatory teams and health authorities to support product approvals.

  • Provide guidance on regulatory requirements across international markets.


4. Regulatory Compliance & Policy Monitoring

  • Monitor updates in international regulatory policies, legislation, and guidance.

  • Ensure regulatory activities comply with global regulatory standards and requirements.

  • Conduct regulatory research and analyze historical precedents to support regulatory decisions.


5. Stakeholder Engagement & Communication

  • Communicate regulatory insights and updates to global project teams.

  • Support health authority queries and regulatory discussions.

  • Build strong partnerships with regional and global regulatory stakeholders.


Required Skills

Regulatory Expertise

  • Strong knowledge of international regulatory frameworks and submission processes

  • Experience with clinical trial applications, marketing authorizations, and lifecycle management

  • Understanding of biotechnology or oncology regulatory environments

Professional Skills

  • Strong analytical and regulatory strategy development capabilities

  • Excellent communication, negotiation, and stakeholder management skills

  • Ability to work in global cross-functional teams


Preferred Qualifications

  • Experience working with global regulatory submissions and international health authorities

  • Knowledge of expedited regulatory pathways and orphan drug designations

  • Familiarity with pediatric plans, compassionate use programs, and regulatory reliance mechanisms


Key Competencies

  • Global regulatory strategy and planning

  • Regulatory submissions and lifecycle management

  • Cross-functional collaboration in pharmaceutical development

  • Regulatory risk assessment and compliance management

  • Strategic stakeholder engagement


About the Company

Amgen is a global biotechnology company dedicated to discovering and delivering innovative medicines for serious diseases. With a strong focus on science, innovation, and patient outcomes, Amgen continues to advance therapies that improve lives worldwide.