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Description
Responsible for managing the regulatory affairs activities throughout the organization. Manages and compiles regulatory submissions in the USA, EU and other jurisdictions as required.
Requirements
Education/Experience
Bachelor’s Degree preferred.
Minimum of 7 years of medical device experience preferably in Quality or Regulatory Affairs.
Full Time
Medical Technology
$115k-152k (estimate)
02/07/2024
06/30/2024
tybermedical.com
BETHLEHEM, PA
50 - 100
2012
Private
JEFF TYBER
$10M - $50M
Medical Technology
Tyber Medical provide Rapid Access to Portfolio Enhancing, Regulatory Approved, Orthopedic Implants.
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