QA Engineer - Operations

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 play an integral part in helping Enovis drive the medical technology industry forward through transforming patient care and creating better patient outcomes.

Job Title:

Quality Assurance Engineer - Operations

Reports To:

Sr. Director, Quality

Location:

Houston Plant (onsite)

Business Unit Description:

Foot and Ankle

High-Level Position Summary:

We are seeking a skilled and experienced Quality Assurance Engineer to join our team. The incumbent provides quality support to manufacturing and supply chain. Focus on nonconforming material program, validation program, and cleanroom support.

Key Responsibilities: The following are the primary duties and responsibilities of this role. Other related duties may be assigned to meet the business need.

• Evaluating nonconforming material and dispositioning based on cross-functional engineering review

• Performing analysis of reports and production data to identify trends

• Initiating, developing, and recommending updates or changes to quality standards and procedures

• Author and review equipment and process validation protocols and reports (IQ/OQ/PQ)

• Responsible for environmental monitoring and dose audit program for sterile devices packaged in Houston cleanroom environment

• Assuring compliance to internal or external specifications and standards (i.e. GMP, ISO, FDA)

• Reviewing trends in device failures associated with nonconforming materials

• Leading root ca