Director, Quality Systems & Compliance

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 & Regulatory Affairs 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:
Director, Quality Systems & Compliance

Reports To:
Chief Regulatory, Quality & Clinical Affairs Officer

Location:
US, Remote

Business Unit Description:
Quality Assurance

Position Summary 

The Director, Quality Systems & Compliance is a key leadership role responsible for driving the evolution, harmonization, and continuous improvement of the company’s global Quality Management System (QMS). This leader will oversee compliance activities across the organization, ensuring adherence to FDA, ISO, MDSAP, EU MDR, and other applicable regulatory requirements. The role will manage the internal and external audit programs, quality metrics, and governance processes to support operational excellence and regulatory readiness across all business units and sites. 

This individual partners closely with crossfunctional leadership—including Operations, R&D, Regulatory Affairs, Clinical Affairs, and Supply Chain—to strengthen the quality culture and ensure the QMS supports scalability, innovation, and sustained compliance. 

Key Responsibilities 

Quality Management System Leadership 

• Lead the design, implementation, and continuous improvement of a unified, enterprise-wide QMS across global sites and business units. 

• Drive QMS standardization, simplification, and integration following mergers, acquisitions, and organizational changes.