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Quality & Regulatory Manager

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Reference Number: TS-2188661657
Date Posted: 09-17-21
Location: Mid Atlantic

Our client is an activity-based medical device company. They are currently seeking a Quality & Regulatory Manager to join their team in the Mid Atlantic.

What's in it for you...
  • Excellent company culture - open, collaborative & professional
  • Very rewarding & impacting role
  • Direct access to Executives
  • Advancement potential
To be considered for an interview, the following experience/skills are desired:
  • Bachelor's degree
  • Class II medical device quality & regulatory experience
  • 510k submission experience
  • Quality systems oversight
  • Knowledge of ISO 13485 and FDA, EU, Canada, Australia medical device regulations
  • Knowledge of statistical methods and sampling techniques
If you experience technical difficulty while applying to the position, please email your resume directly to MedicalDeviceTeam@MRIGlobalMedDevice.com