Quality Engineer - Disposables

Nordson Medical, a global leader in Interventional Solutions, Fluid Components, and Surgical Solutions, is seeking an experienced and highly motivated individual to join our team. We are committed to creating a diverse and inclusive workplace, and we are looking for candidates who share that same commitment.

As a member of our team, you will have the opportunity to work in a dynamic and collaborative environment, where your ideas and contributions will be valued and respected.

Allen, TX | Full‑Time

We are seeking a Quality Engineer I – Disposables to support the Quality Management System (QMS) and ensure the quality and compliance of electronic components and medical devices throughout their lifecycle. This role provides hands‑on support for manufacturing, investigations, and quality processes while developing foundational skills in validation, risk management, and problem‑solving.

The QE I works closely with cross‑functional teams including Manufacturing, Engineering, R&D, Regulatory, and Supply Chain to support product quality and continuous improvement initiatives in a regulated environment.

• Support investigations for nonconformances, complaints, and CAPAs, including data collection and root cause analysis
• Assist in executing CAPA activities and tracking to closure
• Provide day‑to‑day quality engineering support to manufacturing operations
• Support validation activities (IQ/OQ/PQ), test methods, and equipment qualifications
• Assist in developing and updating risk management documentation (FMEAs, risk assessments)
• Review production and quality data to identify trends and improvement opportunities
• Support supplier quality activities, including monitoring performance and corrective actions
• Assist in reviewing engineering changes, procedures, and quality records
• Contribute to continuous improvement and waste reduction initiatives
• Collaborate with cross‑functional teams to ensure compliance with internal and regulatory requirements

• Bachelor’s degree in Engineering or related technical field
• 0–3 years of experience in a quality or engineering role (internships/co‑ops considered)
• Basic knowledge of quality systems (ISO 13485 or regulated environment preferred)
• Familiarity with root cause analysis tools (5 Whys, Fishbone, etc.)
• Exposure to validation concepts (IQ/OQ/PQ) is a plus
• Strong analytical, organizational, and problem‑solving skills
• Effective communication and technical writing abilities
• Ability to manage multiple tasks in a fast‑paced environment

• Internship or experience in medical devices or regulated industry
• Exposure to statistical tools (e.g., Minitab)
• Understanding of risk management concepts (FMEA)

• Build foundational quality engineering experience in the medical device industry
• Work alongside experienced engineers and cross‑functional teams
• Opportunity to grow into advanced quality and leadership roles

If you are interested in being a part of a team and creating an inclusive and diverse workplace, please apply online with your CV.