Quality Engineer I- Disposables

Nordson Corporation • Allen, TX

7d • Onsite

About The Position

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. Summary of the role 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. Quality Engineer I – Electronics 📍 Allen, TX | Full-Time About the Role 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.

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

Nice To Haves

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

Responsibilities

• 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

Benefits

• 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

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level