Medical Device Quality Engineer

Who We Are

ABOUT ENOVIS™

Enovis Corporation (NYSE: ENOV) is an innovation-driven medical technology growth company dedicated to developing clinically differentiated solutions that generate measurably better patient outcomes and transform workflows. Powered by a culture of continuous improvement, global talent and innovation, the Company’s extensive range of products, services and integrated technologies fuels active lifestyles in orthopedics and beyond. For more information about Enovis, please visit www.enovis.com.

What You'll Do

At Enovis™ we pay attention to the details. We embrace collaboration with our partners and patients, and take pride in the pursuit of scientific excellence — with the goal of transforming medical technology as we know it.

Because that’s how we change the lives of patients for the better. And that’s how we create better together. Why work at Enovis? See for yourself.

As a key member of the Quality Team, you will support Enovis in helping drive the medical technology industry forward by supporting quality processes, patient safety, and compliance.

Job Title:

Medical Device Quality Engineer

Reports To:

Sr. Manager, Quality Engineering

Location:

Austin, TX

Business Unit Description:

As a member of the Quality Assurance team, you will support activities that help Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Job Title/High Level Position Summary:
 

Utilizing foundational knowledge of engineering and problem-solving principles, this position is responsible for supporting quality assurance activities related to the implementation, maintenance, and improvement of procedures and work instructions to help ensure safety, quality, and compliance with Company standards and government regulations.

Essential Responsibilities:

• Ensuring compliance with internal and external specifications and standards, including GMP, ISO, FDA, and CMDR requirements. 
• Supporting evaluation of product quality issues that may impact device performance, patient safety, or regulatory compliance. 
• Supporting the evaluation of nonconforming material and assisting with dispositions through cross-functional engineering rev