posted 11/30/2021

Join the GMED team today and work on the frontier of Medical Device Innovation!

Brief job description:

  • Evaluate and assess medical devices for conformity with CE type and design standards for compliance with EU requirements
  • Develop assessment testing procedures
  • Review and evaluate medical devices
  • Identify regulatory classification
  • Compile technical documentation and create technical dossier
  • Manage CE registration processes
  • MS Biomedical Engineering and 12-months related experience

Contact Information: Celeste Gomez at celeste.gomez@lne-gmed.com or humanresources@lne-gmed.com

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GMED North America is an Equal Employment Opportunity Employer, committed to a diverse, inclusive, and healthy work environment with a unique culture.

You are strongly encouraged to submit your resume and your cover letter.

We look forward to hearing from you!