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Director, Labelling Strategy And Governance

GSK plc
5+ years
INR 30 LPA – 40 LPA
Remote
1 June 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: Clinical Trials, Detail-Oriented, Drug Development, Lifesciences, Negotiation Skills, Regulatory Compliance, Communication Skills, CPC Certified, CPT, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, GCP guidelines, HCPCS Level II, ICD-10-CM, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICD-10-PCS

Director, Labelling Strategy and Governance

Employment Type: Full Time
Work Model: Hybrid (Remote & On-site)


Job Overview

The Director, Labelling Strategy and Governance is responsible for leading global labelling strategy, governance, and execution for assigned products across the vaccines and infectious diseases portfolio. The role ensures development of clear, compliant, scientifically accurate, and patient-focused product labelling throughout the entire product lifecycle, from early clinical development through post-approval lifecycle management.

This leadership position combines strategic regulatory expertise, people management, cross-functional collaboration, health authority engagement, and governance oversight to support successful global regulatory outcomes and patient access.


Key Responsibilities

Global Labelling Strategy Leadership

  • Lead development and execution of global labelling strategies for assigned products.

  • Define labelling approaches across:

    • Early Development

    • Clinical Development

    • Registration

    • Post-Approval Lifecycle Management

  • Ensure alignment between global regulatory objectives and product development strategies.

  • Provide strategic guidance on labelling implications for regulatory submissions and development plans.

Labelling Content Development

  • Translate complex clinical, efficacy, and safety data into:

    • Product Information (PI)

    • US Prescribing Information (USPI)

    • EU Summary of Product Characteristics (SmPC)

    • Patient Information Leaflets (PIL)

    • Global Core Labelling Documents

  • Ensure labelling content is:

    • Regulatory-compliant

    • Scientifically accurate

    • Patient-focused

    • Clear and understandable

  • Drive development of plain-language content supporting patient understanding.

Governance & Compliance

  • Represent assigned products and portfolios within global labelling governance forums.

  • Ensure compliance with:

    • Global Regulatory Requirements

    • Regional Regulatory Guidelines

    • Internal Governance Standards

    • Company Policies and Procedures

  • Establish and maintain robust labelling governance processes.

  • Support inspection readiness and regulatory compliance activities.

Cross-Functional Collaboration

  • Partner closely with:

    • Regulatory Affairs

    • Clinical Development

    • Safety & Pharmacovigilance

    • Medical Affairs

    • Commercial Teams

    • Market Access Teams

  • Align stakeholders on labelling strategy and content decisions.

  • Facilitate resolution of complex cross-functional issues.

Health Authority & External Engagement

  • Support and lead regulatory interactions related to product labelling.

  • Engage with:

    • Global Health Authorities

    • Regulatory Agencies

    • Industry Associations

    • Professional Organizations

  • Provide expert labelling input during regulatory discussions and submissions.

  • Monitor evolving regulatory expectations and industry best practices.

People Leadership

  • Lead, coach, and develop a team of global labelling professionals.

  • Drive capability building and succession planning.

  • Foster a culture of accountability, collaboration, and continuous improvement.

  • Support professional development and performance management activities.

Strategic Influence & Stakeholder Management

  • Influence senior leadership and project teams regarding labelling strategy.

  • Communicate complex regulatory and scientific concepts effectively.

  • Present recommendations and strategic decisions to senior stakeholders.

  • Drive consensus across matrix organizations.

Continuous Improvement

  • Identify opportunities to improve:

    • Labelling Processes

    • Governance Frameworks

    • Content Development Practices

    • Regulatory Compliance Approaches

  • Support innovation and modernization initiatives within Regulatory Affairs.

  • Contribute to advancement of global labelling standards and practices.


Qualifications

Education

  • Bachelor's Degree in:

    • Life Sciences

    • Pharmacy

    • Medicine

    • Biotechnology

    • Related Scientific Discipline

Preferred Qualifications

  • Master's Degree (MS)

  • PharmD

  • MD

  • PhD


Experience (Minimum Required)

  • Minimum 5+ years of experience in:

    • Regulatory Affairs

    • Product Labelling

    • Global Regulatory Strategy

  • Demonstrated experience leading:

    • US Prescribing Information (USPI)

    • EU Summary of Product Characteristics (SmPC)

    • Global Labelling Strategies

Preferred Experience

  • Team Leadership and People Management.

  • Regulatory Submission Support.

  • Health Authority Interactions.

  • Vaccines or Infectious Diseases Portfolio Experience.

  • Global Product Lifecycle Management.

  • Matrix Organization Leadership.