Design and develop medical devices and accessories.
Organize projects and maintain Design History Files (DHF)
Write and Submit 510(k)s to the FDA
Use established procedures to improve existing medical devices and accessories.
Continually optimize manufacturing procedures to produce less expensive, higher quality medical devices.
Perform test procedures to verify and validate product quality and efficacy.
Document all developments in scientific notebooks
Complete Document Change Orders (DCO) document and control processes and procedures.
Assist in the completion of new and existing product design validations.
Complete design drawings in Solidworks or similar drafting program and create prototypes to progress the development through its design stages.