Quality Control Lead

About the role

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 .

Responsibilities

• 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.
• Job Title :
• Quality Lead
• Job Profil e :
• Quality Control Technician - 3
• Reports To :
• Manager, Quality Assurance
• Location:
• VMC (Vista Manufacturing Center)
• Business Unit Description :
• Bracing and Supports
• Role Summary :
• Administer and maintain the site training program, ensuring employee training records are current and compliant with QMS requirements.
• Coordinate training assignments, track completion, and support training effectiveness evaluations.
• Partner with department leads to ensure training needs are identified and addressed.
• Update, revise, and maintain controlled procedures, work instructions, and quality documents.
• Support QMS improvements by identifying gaps and contributing to corrective and preventive actions .
• Prepare documentation, records, and evidence for internal audits, customer audits, and regulatory inspections.
• Participate in audit activities and support follow‑up actions to ensure compliance and readiness.
• Oversee QC teams across incoming inspection, in ‑ process inspection, and final product release.
• Assist with inspection planning, sampling, and verification of inspection results.
• Conduct stock checks and inventory verification to ensure product status accuracy.
• Work closely with Quality Engineers to support investigations, root cause analysis, and quality improvement initiatives.
• Coordinate nonconforming material activities, including identification, segregation, documentation, and disposition routing. Ensure timely review and closure of NCMRs, support root‑cause investigations, and collaborate with Quality Engineers, Supply Chain, and Operations to prevent recurrence.
• Minimum Basic Qualifications :
• High school diploma or equivalent required; an associate degree or relevant certification preferred.
• 3 + years of experience in Quality Assurance or Quality Control within manufacturing or other regulated environments.
• Working knowledge of QMS standards (ISO 9001, ISO 13485, AS9100).
• Ability to read and interpret technical drawings, specifications, and inspection data.
• Proficiency with inspection tools, techniques, and basic non ‑ destructive examination methods.
• Experience in using ERP systems (e.g., Oracle) for transactions and reporting.
• Strong communication , documentation, and organizational skills .
• Demonstrated ability to lead or guide quality inspectors and support adherence to SOPs and standard work.
• Effective interpersonal skills, including conflict resolution, collaboration, and active listening.
• Ability to train others and support team development.
• Self ‑ starter capable of working independently and maintaining confidentiality.
• Proficient with computers and general office software.
• Work environment | Physical demands:
• Ability to sit and stand for long periods of time.
• Ability to lift and carry 25 pounds.
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