Quality Control Inspector

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 QA Department 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 Control Inspector

Reports To:
Manager, Quality Assurance

Location:
Vista, CA | On-site

Business Unit Description:
Enovis is a market leader in bracing and supports. Trusted by clinicians, professional athletes and active people from all walks of life, our innovative products and technologies are designed to enhance performance, protection and recovery for the knee, hip, shoulder, back, ankle and more. Our flagship brand, DonJoy, pioneered the concept of functional knee bracing more than 40 years ago. Since then, we have continued to advance bracing technology, reshaped the care path with MotionMD, and added recognized brands to our family, including Aircast, Procare and Exos. Look for us on the field, in the gym and around town.

Job Title/High-Level Position Summary: We are seeking a QA Complaint Inspector to support complaint handling activities within a regulated medical device manufacturing environment. This role is responsible for performing detailed inspections, evaluations, and documentation of returned products and complaint-related materials to ensure compliance with internal procedures, regulatory requirements, and quality standards. The ideal candidate is detail-oriented, analytical, and capable of working both independently and collaboratively to support timely and compliant complaint investigations.

Key Responsibilities:

• Perform inspection, evaluation, and testing of returned medical devices associated with customer complaints
• Conduct visual, functional, and dimensional inspections in accordance with approved procedures and specifications
• Document inspection findings clearly and accurately within complaint handling systems and quality records
• Support sampling and testing activities for complaint investigations, including incoming components or raw materials when required
• Apply approval, rejection, or quarantine identification as appropriate based on inspection outcomes
• Monitor and verify proper functioning of inspection tools, test equipment, and instrumentation used during complaint evaluations
• Collaborate with Quality Engineering, Manufacturing, and Regulatory teams to support root cause analysis and corrective actions
• Assist in drafting or revising inspection procedures and support validation or troubleshooting of test methods when applicable
• Ensure compliance with FDA Quality System Regulation (21 CFR Part 820), ISO 13485, and internal quality system requirements
• Maintain accurate records in accordance with Good Documentation Practices (GDP)
• Support audit readiness by ensuring complaint files and inspection records are complete and compliant

• High school diploma or equivalent (Associate degree in a technical field preferred)
• Minimum 1-2 years of experience in quality inspection, complaint handling, or medical device manufacturing
• Basic knowledge of inspection methods, sampling techniques, and documentation practices in a regulated environment
• Familiarity with inspection tools (calipers, micrometers, gauges) and basic testing equipment
• Working knowledge of Microsoft Office applications (Word, Excel, Outlook)
• Strong written and verbal communication skills
• Ability to follow established procedures and recognize when escalation or deviation from standard practice is required
• Detail-oriented with strong analytical and documentation skills
• Ability to work under general supervision and follow instructions for new or complex tasks

• Familiarity with complaint handling systems (e.g., electronic quality management systems)
• Basic understanding of FDA 21 CFR Part 820 and ISO 13485 requirements
• Ability to stand or sit for extended periods while performing detailed inspection activities
• Ability to lift/pull/carry up to 25 lbs
• Ability to perform repetitive tasks with sustained attention to detail
• Demonstrated ability to work effectively in cross-functional teams within a fast-paced manufacturing environment

• Medical Insurance
• Dental Insurance
• Vision Insurance
• Spending and Savings Accounts
• 401(k) Plan
• Vacation, Sick Leave, and Holidays
• Income Protection Plans
• Discounted Insurance Rates
• Legal Services