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Elevaris Medical Devices
The Quality Engineer, Level II at Elevaris Medical Devices provides quality and compliance support for the manufacture and distribution of medical devices, ensuring adherence to standards such as ISO 13485 and 21 CFR 820. The role involves technical support for complaint investigations, risk management, validations, audits, and continuous improvement activities in an FDA‑regulated environment.
Elevaris Medical Devices is a Contract Development and Manufacturing Organization (CDMO) specializing in procedural needles, precision micro-components, complex tubular components, and sub-assemblies.
Headquarters
San Francisco, CA
Company Size
201-500 employees
Founded
2018
Industry
Technology
Glassdoor Rating
4.2 / 5
Sarah Johnson
Chief Executive Officer
Michael Chen
Chief Technology Officer
Emily Williams
VP of Engineering
David Rodriguez
VP of Product
Jessica Thompson
Chief Financial Officer
Andrew Park
VP of Sales
View leadership team, funding history,
and employee contacts for Elevaris Medical Devices.
Right around the average for this role