Quality Technician

Overview

Micro Aire Surgical Instruments LLC, part of the global Marmon Holdings organization backed by Berkshire Hathaway, offers learning and growth opportunities and a culture that empowers employees to be their best.

Micro Aire, Who We Are Micro Aire Surgical Instruments (Charlottesville, VA) is a wholly-owned subsidiary and one of five companies within the Medical Group of Marmon Holdings, a Berkshire Hathaway company. Micro Aire is a mid-sized medical device solutions company with a 45-year legacy of quality and innovation. With well-recognized brands, the company is positioned as a leader in specialty markets, including minimally invasive medical devices and equipment for aesthetics/reconstruction, endoscopic soft tissue release, and orthopedic accessories.

Micro Aire designs, manufactures, and markets cutting-edge medical devices that empower surgeons to push the boundaries of surgical precision, delivering safe, efficient, and high-quality patient outcomes.

The Quality Technician supports Quality Assurance and Quality Control functions to ensure products meet established standards and regulatory requirements. This role is mainly responsible for performing incoming inspections and supporting product release activities. Other responsibilities may include maintaining and improving quality documentation and assisting with validation, auditing, and nonconformance processes. The Quality Technician partners cross-functionally to drive continuous improvement, ensure compliance, and uphold product quality throughout the manufacturing lifecycle.

As a Quality Technician
, you’ll play a critical role in maintaining product excellence and supporting continuous improvement initiatives.

Key responsibilities include:

• Perform incoming, in-process, and final inspections to ensure product quality and compliance
• Execute final QA release activities, including specialized product lines (Endotine/Ultratine)
• Update quality documentation and drive improvements through Document Change Orders (DCOs)
• Support test method validations and Gage R&R studies
• Assist with MRB/NCMR processes, including inventory control and corrective actions
• Contribute to validation activities (protocol development, execution, reporting)
• Participate in CAPA, complaint evaluations, and Temporary Deviations (TDs)
• Conduct or support internal audits and quality system improvements
• Partner cross-functionally to support NPD and design changes

We’re looking for someone who thrives in a detail-oriented, collaborative environment:

• Associate’s degree in Science, Engineering, or related field or 2+ years of relevant manufacturing experience
• Strong understanding of quality processes and documentation
• Experience with measurement tools, data interpretation, and basic statistics
• Familiarity with ERP systems and Microsoft Office
• Knowledge of GD&T (preferred)
• Excellent communication skills and attention to detail
• A mindset focused on continuous improvement and accuracy

Apply today and help us maintain the highest standards in medical manufacturing while advancing your career in quality.

• Competitive compensation
• 401K with company match
• Medical/Dental/Vision
• Vacation & Paid Holidays
• Connection with Marmon Holdings company wide initiatives

Following receipt of a conditional offer of employment, candidates will be required to complete additional job-related screening processes as permitted or required by applicable law.

We are an equal opportunity employer, and all applicants will be considered for employment without attention to their membership in any protected class. If you require any reasonable accommodation to complete your application or any part of the recruiting process, please email your request to , and please be sure to include the title and the location of the position for which you are applying.