Executive Director, Csrm Device And Product Quality

539

Multiple Locations
Base: $310,900.00 - $489,400.00; bonus/equity: ann...
Hybrid
Medical device safety strategy
Product quality medical assessment
Global regulatory requirements
Provides strategic and operational leadership for a global Center of Excellence delivering medical and scientific expertise in device safety, health hazard oversight, and product quality medical risk assessment

Job Summary

  • Provides strategic and operational leadership for a global Center of Excellence delivering medical and scientific expertise in device safety, health hazard oversight, and product quality medical risk assessment.
  • Leads cross‑functional collaboration across CSRM Therapeutic Area leadership, device development, commercial, manufacturing, and regulatory organizations to ensure patient safety, regulatory compliance, and successful execution of the Company’s product portfolio.
  • The successful candidate will be eligible for annual bonus and long-term incentive, if applicable, and offered a comprehensive package of benefits including medical, dental, vision, and retirement benefits.

Matching Summary

Provides strategic and operational leadership for a global Center of Excellence delivering medical and scientific expertise in device safety, health hazard oversight, and product quality medical risk assessment.

Salary

Base: $310,900.00 - $489,400.00; Bonus/Equity: Annual bonus and long-term incentive, if applicable; Benefits: Medical, dental, vision healthcare and other insurance benefits (for employee and family), retirement benefits, including 401(k), paid holidays, vacation, and compassionate and sick days.

Skills & Requirements

Must-have

  • Medical device safety strategy
  • Product quality medical assessment
  • Global regulatory requirements
  • Cross-functional leadership
  • Patient safety oversight

Nice-to-have

  • High-performing team culture
  • Scientifically rigorous approach
  • Ethical standards alignment
  • Enterprise decision-making influence

Key Requirements

  • MD with 7-12 years experience
  • 3-5 years supporting manufacturing safety/drug device development
  • Global regulatory agencies familiarity
  • Leadership experience building teams

Work Rights

Not specified

Tailored Resume

Cover Letter