Vp, Global Regulatory Affairs Heart Recovery

Johnson & Johnson Med Tech

Danvers, Massachusetts, United States of America
Base: $218,000.00 - $401,350.00; bonus/equity: eli...
Global regulatory affairs strategy
Class iii device experience
Cardiovascular disease domain expertise
The VP of Global Regulatory Affairs will be responsible for directing all regulatory affairs activities for Heart Recovery to ensure the business unit, corporate and agency global product registration and compliance objectives are met

Job Summary

  • The VP of Global Regulatory Affairs will be responsible for directing all regulatory affairs activities for Heart Recovery to ensure the business unit, corporate and agency global product registration and compliance objectives are met.
  • This role develops methodology for the business unit’s Regulatory Affairs strategies, assessments, and policies accounting for new and changing government regulations.
  • Creates a purpose driven culture in which decisions and actions are strategically informed by patients, customers, and employee needs by aligning Johnson & Johnson’s Credo and Leadership Imperatives with the strategies and goals of the team and enterprise.

Matching Summary

The VP of Global Regulatory Affairs will be responsible for directing all regulatory affairs activities for Heart Recovery to ensure the business unit, corporate and agency global product registration and compliance objectives are met.

Salary

Base: $218,000.00 - $401,350.00; Bonus/Equity: Eligible for long-term incentive program; Benefits: 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 Regulatory Affairs strategy
  • Class III device experience
  • Cardiovascular disease domain expertise
  • FDA and international regulatory bodies interaction
  • Regulatory submissions and lifecycle planning

Nice-to-have

  • Cross-functional influence and stakeholder alignment
  • Talent development and coaching
  • Crisis leadership
  • Driving convergence between policy and plans
  • Patient-centric decision making

Key Requirements

  • 15+ years of Regulatory Affairs experience
  • 8 years leading high performing teams
  • Class III device experience required
  • Advanced Degree (Masters, PhD, MD) preferred

Work Rights

Not specified

Tailored Resume

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