Project Manager, Impella Connect

Johnson & Johnson

Danvers, Massachusetts, United States of America
Base: $117,000.00 - $201,250.00; bonus/equity: eli...
Hybrid
Global compliance certifications
Iso27001, c5, soc2 compliance
Impella connect development and operations
This critical role involves leading the establishment and maintenance of global compliance certifications required to maintain and expand the global usage of a connected cloud service, Impella Connect

Job Summary

  • This critical role involves leading the establishment and maintenance of global compliance certifications required to maintain and expand the global usage of a connected cloud service, Impella Connect.
  • You will be responsible for project coordination, identifying and driving opportunities for synergies, managing project timelines, risks, dependencies, and communication, and supporting compliance audit processes.
  • The role requires a BS/BA with 6 years of work experience, including 5+ years leading product related projects in medical device or related high-compliance/regulated industry, with an understanding of design controls, risk management, and global regulatory and compliance requirements.

Matching Summary

This critical role involves leading the establishment and maintenance of global compliance certifications required to maintain and expand the global usage of a connected cloud service, Impella Connect.

Salary

Base: $117,000.00 - $201,250.00; 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 compliance certifications
  • ISO27001, C5, SOC2 compliance
  • Impella Connect development and operations
  • project timelines, risks, dependencies
  • cross-functional team leadership

Nice-to-have

  • improving cardiovascular possibilities
  • reimagining how we heal
  • continuous improvement of SOPs
  • collaboration across broader JnJ organization

Key Requirements

  • BS/BA
  • 6 years of work experience
  • 5+ years experience leading product related projects
  • medical device or related high-compliance/regulated industry
  • understanding of design controls, risk management, and global regulatory and compliance requirements (FDA, ISO)
  • Exceptional project coordination skills
  • Excellent verbal and written communication
  • Demonstrated leadership in cross-functional teams

Work Rights

Not specified

Tailored Resume

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