Support manufacturing troubleshooting, process documentation, and continuous improvement projects.
Execute equipment validation protocols and assist with engineering change orders.
Analyze production data and participate in root cause investigations.
Draft technical reports and learn medical device regulatory standards.
What they're looking for
Students pursuing a Bachelor’s degree in engineering or related fields.
Strong organizational skills and interest in medical device manufacturing.
Proficiency in Microsoft Office; SolidWorks or CAD experience is preferred.
Ability to work independently and communicate effectively.
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.
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.
If you are interested in being a part of a team and creating an inclusive and diverse workplace, please apply online with your CV.
About Nordson Medical
At Nordson MEDICAL, you don't have to be a doctor to help save lives. We are the global expert in the design, development, and manufacturing of complex medical devices and component technologies. By joining our team today, you will help us bring innovative ideas to life. Nordson MEDICAL is a global team that works to create components for life-saving medical devices. We offer a supportive culture in a growing and dynamic work environment. Whether you're just beginning your career or you're a seasoned professional, there's a place for you to belong at Nordson MEDICAL. We offer hourly and salary positions in production, maintenance, customer service, quality, engineering, and more. We actively invest in our teams to help you build your skillsets and advance your career.
From Nordson's public posting, laid out for reading by newgrad.ai with the wording unchanged. Check the original before you apply.
