MicroAire Surgical Instruments LLC
As a part of the global industrial organization Marmon Holdings-which is backed by Berkshire Hathaway-you'll be doing things that matter, leading at every level, and winning a better way. We're committed to making a positive impact on the world, providing you with diverse learning and working opportunities, and fostering a culture where everyone's empowered to be their best.
The Principal Quality Assurance Engineer is a lead member of the Quality Assurance team. This individual is a technical expert and provides technical leadership for quality activities associated with the development of new medical devices and the continued support of current medical devices. The Principal Quality Assurance Engineer leads the overall activities including CAPAs, customer complaints, MRB/NCMRs, supplier quality, validations (equipment, process, test methods and software), design controls, process improvement, risk management, and internal audits. Also weighs in needed department resources as well as resource utilization. This individual will work with internal customers, external customers, and suppliers as the technical voice that will derive quality requirements. Requires comprehensive mechanical and technical problem-solving skills. The Principal QAE is responsible for mentoring QAEs, taking the lead on QAE projects, and will serve as a subject matter expert for QAE operations.
Essential Duties and Responsibilities
Supports New Product Development/Design Control, performing quality engineering activities such as design inputs, design outputs, design verification, design validation, design transfer, and risk analysis/ management. Ensures compliance to specifications and regulatory requirements and identifies opportunities to improve product and process quality. Assists with the compliance of national and international standards and regulations. Conducts analysis including design of experiments, as needed.
Generates qualification verification, and/or validation plans, protocols, and reports for new or updated manufacturing processes and equipment (IQ/OQ/PQ). Understands the integration of component, design and process to ensure adequate process capability. Drives the use of statistical analysis tools to understand process capability.
Reviews product and process changes and assesses impact on product reliability and qualification/validation status. Assists in changing implementation.
Leads and participates in quality metrics reviews; identifying weaknesses and risks associated with MicroAire products and tracking the mitigation of those issues throughout the corrective action process.
Facilitates and aids cross-functional teams in performing complaint investigations and CAPA activities.
Dispositions any materials/components that are rejected for non-conformance with effective corrective actions.
Coordinates and consults with suppliers and supply chain to improve quality, cost and delivery from suppliers. Works with incoming inspection to ensure adequate and robust quality inspections. Performs gauge R&R, capability analysis, etc as required.
Available to provide support for outside sales force and customers to resolve product technical questions and instrument performance concerns, as needed.
Education and Experience
Bachelor's degree in related field (engineering degree preferred)
At least 8 years of Quality Assurance manufacturing (mechanical and electrical) experience in the medical device industry.
American Society for Quality, Certified Quality Engineer (CQE) or equivalent required.
Lean-Six-Sigma experience preferred.
Competencies
Competency
Skills
Behaviors
Quality Systems & Regulatory Compliance-
Demonstrates deep expertise in medical device quality systems, regulations, standards, and compliance requirements to ensure products and processes consistently meet regulatory and quality expectations.
Technical Problem Solving & Risk Management-
Applies advanced engineering principles, statistical methods, and risk-based thinking to investigate issues, identify root causes, and implement sustainable solutions.
Validation & Design Assurance-
Ensures products, equipment, software, and manufacturing processes are appropriately verified and validated to meet intended use requirements and quality standards.
Cross-Functional Leadership & Influence-
Leads quality initiatives and influences decisions across engineering, operations, supply chain, regulatory, and commercial teams without direct authority.
Coaching, Mentoring & Technical Expertise-
Develops organizational capability by sharing technical knowledge, mentoring team members, and serving as the subject matter expert for quality engineering practices.
Mentoring and coaching
Technical training
Knowledge transfer
Performance guidance
Continuous improvement methodologies
Subject matter expertise
Provides guidance to QA Engineers and cross-functional teams
Shares best practices and lessons learned proactively
Elevates team technical capability and problem-solving skills
Acts as the go-to expert for complex quality engineering issues
Work Environment, Physical Demands and Protective Equipment
Supervision: No direct reports. Acts as a mentor and technical expert resource
See MicroAire Training Management System
ASQ Certifications preferred.
All required training for this role is documented in the individual training matrix within the MicroAire Training Management System and must be completed accordingly.
Schedule, Travel Responsibility, Special Conditions or Requirements
Works in an office environment.
Periodic work in various manufacturing environments.
Occasional travel may be required.
Prolonged periods sitting at a desk and working on a computer.
Must be able to traverse the production facility.
Must be able to lift up to 25 pounds at a time.
List any special conditions or requirements that apply to the position, such as the ability to work weekends.
Pay Range: $112,000-$136,000
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 careers@marmon.com, and please be sure to include the title and the location of the position for which you are applying.
| Location | Charlottesville, VA |
| Salary | $112,000–$136,000 Per Year |
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