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Acerca del Rol
Are you passionate about quality and compliance in the medical device industry? Join our team as a Quality Management System Coordinator and play a key role in ensuring our systems meet top regulatory standards like ISO 13485 and 21 CFR 820.
We're looking for a detail-oriented professional with strong knowledge in QMS processes and a drive for continuous improvement. If you're ready to guide teams, monitor critical quality activities, and support our mission of excellence, this could be your next big opportunity.
Requerimientos
US Visa
English - C1
Professional in Biomedical Engineering or related careers.
1 year in related positions
ISO 13485:2016 knowledge
Desired: 21 CFR 820 knowledge
Desired: ED MDR 2017/745
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