Intern (Disposables Engineering)

Nordson Corporation; Allen (TX); Hybrid; USD 25,000 - 34,000; Full time

Job summary

Nordson Medical in Allen, Texas, is seeking an Intern in Disposables Engineering to support manufacturing processes, troubleshoot, document, and pursue continuous improvement under guidance.

You will assist in validation protocols, analyze production data, and learn Lean and Six Sigma; exposure to FDA QSR and ISO 13485 will be provided. This internship targets engineering students with strong communication and teamwork skills.

Qualifications

• Pursuing a Bachelor’s degree in Mechanical, Industrial, Manufacturing, Biomedical Engineering or related field.
• Previous internship, co-op, or project experience in regulated manufacturing or medical device environment is a plus.
• Strong organization, time management and communication abilities; open to learning Lean/Six Sigma concepts.

Responsibilities

• Assist in sustaining manufacturing processes through troubleshooting, documentation, and continuous improvement.
• Support validation/qualification protocols (IQ/OQ/PQ) for equipment, processes, and design changes.
• Collaborate with engineers to identify process improvements for safety, quality and throughput.
• Follow ECO documentation, test execution and implementation activities.
• Analyze production data, perform basic statistics, and summarize findings in reports.
• Learn and apply FDA QSR and ISO 13485 quality standards.

Skills

Organizational skills

Time management

Communication skills

Excel

SolidWorks

CAD

Root cause analysis

Data analysis

Engineering documentation

Education

Bachelor’s degree in Mechanical/Industrial/Manufacturing/Biomedical Engineering

Tools

SolidWorks

CAD

Microsoft Excel

Job description

## Intern (Disposables Engineering)Apply: USA - Texas - Allen: Full time: Posted Yesterday: REQ52924**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.**Essential Job Duties and Responsibilities*** Assist in sustaining manufacturing processes by supporting troubleshooting, documentation, and continuous improvement activities.* Support execution of validation and qualification protocols (IQ/OQ/PQ) for equipment, processes, and design changes.* Collaborate with engineers to identify and implement process improvements that enhance safety, quality, and throughput.* Participate in engineering change order (ECO) documentation, test execution, and implementation activities.* Help analyze production data, perform basic statistical analysis, and summarize findings in reports.* Observe and participate in root cause analysis activities and nonconformance investigations.* Learn and apply Lean and Six Sigma principles to reduce waste and improve efficiency.* Participate in design reviews and contribute DFM (Design for Manufacturability) input under guidance.* Assist in drafting technical documents, validation plans, and troubleshooting guides.* Learn quality and regulatory standards applicable to medical devices, including FDA QSR and ISO 13485**Education and Experience Requirements*** Pursuing a Bachelor’s degree in Mechanical, Industrial, Manufacturing, Biomedical Engineering, or related field.* Previous internship, co-op, or project experience in regulated manufacturing or medical device environment is a plus.**Required Skills and Abilities*** Strong organizational and time management skills with the ability to independently complete assigned tasks.* Strong interest in medical device manufacturing and continuous improvement.* Effective written and verbal communication skills.* Detail-oriented and self-motivated with the ability to follow directions and ask questions.* Familiarity with Microsoft Office (Word, Excel, PowerPoint); exposure to SolidWorks or CAD is preferred.* Basic understanding of root cause analysis, data analysis, and engineering documentation.**Interested?**If you are interested in being a part of a team and creating an inclusive and diverse workplace, please apply online with your CV.