Quality Compliance Manager - ECMP Site Facilitator

Integra LifeSciences
Memphis, NJ
Job Description
Joining Integra LifeSciences is a chance to do important work that creates change and shapes the future of healthcare. The Quality Compliance Manager, ECMP Site Facilitator, provides tactical support and oversight of the implementation of the Enterprise Compliance Master Plan at Integra LifeSciences sites.

Requirements

  • Bachelor's degree in Engineering, Science, or closely related technical discipline
  • 10+ years of experience leading a team or equivalent education and years of management experience
  • Experience working Quality Management Systems and understanding compliance
  • Experience in highly regulated industries, medical device and/or pharmaceutical preferred, including material remediation experience
  • Experience in implementing remediation programs, and working with compliance frameworks such as FDA, ISO 13485, and EU MDR
  • Demonstrated management and communication skills, proven track record of cross-functional collaboration across teams and change management skills

Benefits

  • Medical, dental, vision, life insurance, short- and long-term disability, business accident insurance, and group legal insurance
  • Savings plan (401(k))
  • Generous Paid Time Off
  • 401k Matching
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