Supplier Quality Assurance 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

Job Description

At Enovis™ we sweat the little things. We embrace collaboration with our partners and patients, and we glory in the grind 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.

As a key member of the Quality Assurance 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

Reports To: Manager, Quality Assurance

Location: Vista, CA | On-site

Travel requirements: Up to 20% (domestic and international supplier sites)

Work Authorization: Must be authorized to work in the U.S. (No visa sponsorship available)

Role Summary:

We are seeking a dynamic Supplier Quality & Quality Systems Engineer to manage supplier quality programs and drive compliance and performance across our site's quality system. This role supports supplier qualification and performance, leads internal and external audits, facilitates regulatory body inspections, and ensures alignment with product safety and registration requirements. The ideal candidate will be experienced in both supplier quality and quality systems within the medical device industry.

Key Responsibilities:

• Lead supplier audits, assessments, and corrective action processes (SCARs)
• Manage supplier performance metrics, scorecards, and improvement plans
• Support product safety registration processes (e.g., CE, UL, FDA submissions), including coordination with Regulatory Affairs
• Own and drive the site’s CAPA, NCMR, and training processes
• Support the development and validation of supplier-provided components and materials
• Drive root cause investigations for supplier-related nonconformances (NCMRs, SCARs)
• Collaborate with R  
• Lead and support internal audits; coordinate and prepare for external and regulatory body inspections (FDA, ISO, MDSAP)