Job Summary

The Quality Engineer is responsible to ensure compliance in product and process development, validations and process optimization, line support, acceptance sampling, and continuous improvement for Class III medical devices. This is a hands-on role where the Quality Engineer will apply intensive, self-directed and diversified knowledge of engineering and quality principles and practices for implantable medical devices and accessories. Will work independently with little to no supervision and exercise considerable discretion in determining objectives and approaches to significant organizational projects or assignments.

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Role Requirements

Applying knowledge of QSR and GMP requirements on a daily basis, the duties and responsibilities for this position include, but are not limited to, the following: