Quality Engineer 3
Date: Dec 5, 2025
Location: Trenton, GA, US
Company: Teleflex
Expected Travel: Up to 10%
Requisition ID: 13128
About Teleflex Incorporated
As a global provider of medical technologies, Teleflex is driven by our purpose to improve the health and quality of people’s lives. Through our vision to become the most trusted partner in healthcare, we offer a diverse portfolio with solutions in the therapy areas of anesthesia, emergency medicine, interventional cardiology and radiology, surgical, vascular access, and urology. We believe that the potential of great people, purpose-driven innovation, and world-class products can shape the future direction of healthcare.
Teleflex is the home of Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ – trusted brands united by a common sense of purpose.
At Teleflex, we are empowering the future of healthcare. For more information, please visit teleflex.com.
OEM – Teleflex Medical OEM is a leading global provider of product development and production services for medical device manufacturers. We set ourselves apart with deep expertise, decades of experience, a dedication to design for manufacturability, and extensive, in-house capabilities, which include engineering, regulatory services, material selection and formulation, prototyping, manufacturing, assembly and packaging. We deliver industry-changing innovations and next-generation solutions for extrusions; diagnostic and interventional catheters; balloons and balloon catheters; sheath/dilator sets; specialty sutures, braids and fibers; and bioabsorbable sutures, yarns and resins. Join a dynamic, growing team that offers healthcare providers an array of medical technology solutions that make a difference in patients’ lives.
Position Summary
This position will provide technical support and take a leadership role in quality engineering functions in manufacturing and product development in compliance with FDA 21CFR Part 820, ISO 13485, and internal procedures.
Principal Responsibilities
• Support product and process validation, design change and review, quality planning, and risk evaluation.
• Supervise Quality Assurance Inspectors if needed.
• Coordinate Corrective and Preventive Action (CAPA) for customer, internal, and vendor related needs.
• Audit internal and vendor processes and procedures.
• Participate in Continuous Improvement Projects (CIP) for both processes and business systems.
• Direct quality activities in manufacturing such as inspection methods and Material Review Board (MRB).
• Develop training programs for inspection and engineering.
• Represent company during customer or regulatory audits as needed.
Education / Experience Requirements
• Must have a B.S. (technical degree preferred)
• Minimum 5-8 years QA engineering discipline in a high regulated area
• ASQ certification highly desired
• Medical device experience preferred
ISO 13485 regulation knowledge
Specialized Skills / Other Requirements
• Validation concepts & techniques (process, equipment, and gauging)
• Regulatory cGMP, QSR and ISO knowledge base
• Computer literate (MS Word, Excel, Access, PowerPoint, and Mini-tab preferred)
• Negotiation and problem solving skills
• Good oral and written communication skills
• Statistical Skills (DOE, SPC, Reliability, Gage R&R)
• Experience with risk analysis methodologies
• Experience in the area of manufacturing operations
• Ability to prioritize and work independently
• Experience developing training programs
• Able to work independently with limited supervision
• Exposure to high production/output machinery and equipment, and constant noise in the production/plant environment. Engages in walking, sitting, lifting, bending, carrying, talking, and hearing
• The job description documents the general nature and level of work but is not intended to be a comprehensive list of all activities, duties, and responsibilities required of job incumbents. Consequently, job incumbents may be asked to perform other duties as required.
Working Conditions / Physical Demands
TRAVEL REQUIRED: 10 %
WORKING ENVIRONMENT:
☐ Office/Professional ☒ Plant/Manufacturing ☐ Remote/Field ☐ Laboratory
At Teleflex, we follow a comprehensive hiring process. We do not accept unsolicited resumes from agency recruiters or 3rd party firms. We do not make unsolicited job offers. We do not ask for money or require equipment purchase up-front.
Teleflex Incorporated is an equal opportunity employer. Applicants will be considered without regard to age, race, religion, color, national origin, ancestry, sexual orientation, disability, nationality, sex, or veteran status. If you require accommodation to apply for a position, please contact us at: 877-880-8588 or Talent@Teleflex.com.
Teleflex, the Teleflex logo, Arrow™, Barrigel™, Deknatel™, LMA™, Pilling™, QuikClot™, Rüsch™, UroLift™ and Weck™ are trademarks or registered trademarks of Teleflex Incorporated or its affiliates, in the U.S. and/or other countries.
© 2025 Teleflex Incorporated. All rights reserved.
Nearest Major Market: Chattanooga