Executive Director, Csrm Device And Product Quality

Muckelab

Base: $310,900.00 - $489,400.00; bonus/equity: eli...
Hybrid (3 days onsite, 1 day remote)
Medical device safety expertise
Product quality medical risk assessment
Global regulatory requirements
The Executive Director, CSRM Device and Product Quality at Muckelab is responsible for leading a global Center of Excellence focused on device safety, health hazard oversight, and product quality medical risk assessment. This strategic role emphasizes cross-functional collaboration and compliance throughout the product lifecycle, requiring a strong background in clinical safety and medical device regulations

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.
  • Leads and develops a global Center of Excellence comprised of approximately 8–10 physicians and scientists with expertise in device and product quality safety.

Matching Summary

Match Score: 85

The Executive Director, CSRM Device and Product Quality at Muckelab is responsible for leading a global Center of Excellence focused on device safety, health hazard oversight, and product quality medical risk assessment. This strategic role emphasizes cross-functional collaboration and compliance throughout the product lifecycle, requiring a strong background in clinical safety and medical device regulations.

Salary

Base: $310,900.00 - $489,400.00; Bonus/Equity: Eligible for annual bonus and long-term incentive; Benefits: Comprehensive package including medical, dental, vision, 401(k), paid holidays, vacation, sick days

Skills & Requirements

Must-have

  • Medical device safety expertise
  • Product quality medical risk assessment
  • Global regulatory requirements
  • Cross-functional collaboration
  • Patient safety and regulatory compliance

Nice-to-have

  • High-performing team culture
  • Scientifically rigorous team
  • Ethical standards
  • Enterprise leader influencing decisions

Key Requirements

  • M.D. with 7-12 years relevant experience
  • 3-5 years supporting manufacturing safety/drug device development
  • Thorough familiarity with global regulatory agencies
  • Proven leadership capability
  • Outstanding interpersonal, communication, and negotiation skills

Work Rights

Not specified

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