Associate Director, Global Labeling Product Leader

J&J FAMILY OF COMPANIES

High Wycombe, United Kingdom
Hybrid
Global labeling strategy development
Regulatory labeling content expertise
Cross-functional team leadership
Johnson & Johnson is seeking an Associate Director, Global Labeling Product Leader to drive global labeling strategies in a hybrid role based in High Wycombe, UK. The ideal candidate will possess extensive regulatory labeling experience in the pharmaceutical sector and will collaborate across various functional teams to ensure compliance and quality in labeling documents

Job Summary

  • Johnson & Johnson is committed to healthcare innovation to prevent, treat, and cure complex diseases with smarter and less invasive treatments.
  • The Associate Director, Global Labeling Product Leader will drive global labeling strategy, lead cross-functional teams, and ensure alignment with regulatory and product strategies.
  • This role supports global labeling inspections and audits, collaborates with external partners, and contributes to continuous improvement of labeling processes.

Matching Summary

Match Score: 85

Johnson & Johnson is seeking an Associate Director, Global Labeling Product Leader to drive global labeling strategies in a hybrid role based in High Wycombe, UK. The ideal candidate will possess extensive regulatory labeling experience in the pharmaceutical sector and will collaborate across various functional teams to ensure compliance and quality in labeling documents.

Skills & Requirements

Must-have

  • Global labeling strategy development
  • Regulatory labeling content expertise
  • Cross-functional team leadership
  • Knowledge of worldwide regulatory guidelines
  • Labeling document management
  • Project management in matrix environment

Nice-to-have

  • Collaborative customer-focused culture
  • Continuous improvement leadership
  • Experience with New Molecular Entity submissions
  • Strong negotiation and partnering skills
  • Ability to manage complex compounds labeling

Key Requirements

  • Minimum Bachelor’s degree in scientific discipline
  • 8+ years professional experience
  • 6+ years regulatory labeling content experience
  • Pharmaceutical industry experience required
  • Understanding of drug development
  • Experience leading project teams
  • Experience with document management systems

Work Rights

Not specified

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