Quality Control Inspector

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

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

Minimum Basic Qualifications:

• 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

Travel Requirements: Not required.

Desired Characteristics:

• 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

Currently, Enovis does not provide sponsorship for employment visas (e.g., H-1B) and will not offer such sponsorship in the future. Applicants must already have full-time work authorization in the United States, both now and in the future, without requiring sponsorship.

"Creating better together". It's the Enovis purpose, and it's what drives us and empowers us every day on a global scale. We know that the power to create better - for our customers, our team members, and our shareholders - begins with having the best team, pursuing common goals, operating at the highest levels, and delivering extraordinary outcomes.

What does creating better together mean to us at Enovis? Discover the "why" behind our purpose, values and behaviors:

Our Enovis Purpose, Values and Behaviors on Vimeo

We offer a comprehensive benefits package that includes:

• 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

Join us in creating better together.

EQUAL EMPLOYMENT OPPORTUNITY
Enovis provides equal employment opportunities based on merit, experience, and other work-related criteria without regard to race, color, ethnicity, religion, national origin, sex, age, pregnancy, disability, veteran status, or any other status protected by applicable law. We also strive to provide reasonable accommodation to employees' beliefs and practices that do not conflict with Enovis policies and applicable law. We value the unique contributions that every employee brings to their role with Enovis.