Vp, Global Regulatory Affairs Heart Recovery

Johnson & Johnson

Danvers, Massachusetts, United States of America
Base: $218,000.00 - $401,350.00; bonus/equity: eli...
Cardiovascular regulatory expertise
Class iii medical device experience
Regulatory strategy and policy development
Johnson & Johnson Med Tech is recruiting a Vice President of Global Regulatory Affairs, Heart Recovery to lead regulatory activities and ensure compliance for cardiovascular products

Job Summary

  • Johnson & Johnson Med Tech is recruiting a Vice President of Global Regulatory Affairs, Heart Recovery to lead regulatory activities and ensure compliance for cardiovascular products.
  • The role involves developing regulatory strategies, managing multiple teams, and collaborating with internal and external stakeholders to drive innovation and timely product commercialization.
  • Employees are eligible for comprehensive benefits including retirement plans, long-term incentives, various types of leave, and a culture aligned with Johnson & Johnson’s Credo and Leadership Imperatives.

Matching Summary

Johnson & Johnson Med Tech is recruiting a Vice President of Global Regulatory Affairs, Heart Recovery to lead regulatory activities and ensure compliance for cardiovascular products.

Salary

Base: $218,000.00 - $401,350.00; Bonus/Equity: Eligible for long-term incentive program; Benefits: Retirement plans, vacation, sick leave, parental leave, and other paid time off

Skills & Requirements

Must-have

  • Cardiovascular regulatory expertise
  • Class III medical device experience
  • Regulatory strategy and policy development
  • Cross-functional stakeholder collaboration
  • Regulatory submissions and compliance management
  • Leadership of high performing teams
  • FDA and international regulatory interactions

Nice-to-have

  • Inclusive leadership and talent development
  • Continuous improvement and innovation focus
  • Scientific writing and data interpretation
  • Regulatory intelligence and government affairs
  • Project management and regulatory operations
  • Legal and labeling compliance interface

Key Requirements

  • 15+ years regulatory affairs experience
  • Minimum 8 years leadership experience
  • Bachelor’s degree in Life Sciences or related field
  • Advanced degree preferred (Masters, PhD, MD)
  • Class III device regulatory experience required
  • Ability to travel up to 30%

Work Rights

Not specified

Tailored Resume

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