Associate Director, Global Labeling Product Leader

Johnson & Johnson MedTech

Horsham, Pennsylvania, United States of America
Base: $137,000.00 - $235,750.00; bonus/equity: not...
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Global labeling strategy
Labeling development and content
Health authority discussions
** Johnson & Johnson MedTech is seeking an Associate Director, Global Labeling Product Leader, to drive global labeling strategy and collaborate on regulatory affairs for pharmaceutical products. The ideal candidate will have extensive experience in regulatory labeling, strong communication skills, and a collaborative mindset. **

Job Summary

  • Drive the global labeling strategy, including demonstrating an understanding of competitors in the therapeutic area, their development plans and status and knowledge of labeling aspects for labeling development and target labeling for new products.
  • Lead the development, revision, review, agreement, and maintenance of target labeling, primary labeling (Company Core Data Sheet (CCDS), United States Package Insert (USPI) and associated patient labeling, European Union Product Information (EUPI), and derived documents) for assigned compounds.
  • The anticipated base pay range for this position is : $137,000.00 - $235,750.00; Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).

Matching Summary

Match Score: 75

** Johnson & Johnson MedTech is seeking an Associate Director, Global Labeling Product Leader, to drive global labeling strategy and collaborate on regulatory affairs for pharmaceutical products. The ideal candidate will have extensive experience in regulatory labeling, strong communication skills, and a collaborative mindset. **

Salary

Base: $137,000.00 - $235,750.00; Bonus/Equity: Not specified; Benefits: Eligible for Company’s consolidated retirement plan (pension) and savings plan (401(k)), long-term incentive program, vacation, sick time, holiday pay, Work/Personal/Family Time, Parental Leave, Bereavement Leave, Caregiver Leave, Volunteer Leave, Military Spouse Time-Off

Skills & Requirements

Must-have

  • global labeling strategy
  • labeling development and content
  • Health Authority discussions
  • cross-functional team leadership
  • scientific integrity
  • continuous process improvement

Nice-to-have

  • customer-focused learning culture
  • managing complex compounds
  • driving collaborative culture

Key Requirements

  • Bachelor’s degree in a scientific discipline
  • 8 years of professional work experience
  • 6 years of direct regulatory labeling content experience
  • Relevant pharmaceutical industry experience
  • Understanding of pharmaceutical drug development
  • Experience leading project teams in a matrix environment
  • Experience leading continuous improvement projects
  • Experience working with document management systems

Work Rights

Not specified

Tailored Resume

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