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Intern - Design Assurance (Spring 2027) at Plexus Deutschland GmbH

Neenah, Wisconsin, United States -

Full Time

Start Date

Immediate

Expiry Date

15 Apr, 26

Salary

0.0

Posted On

15 Jan, 26

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Prototyping, Documentation, Technical Assistance, Debug Techniques, Electro-Mechanical Products, Regulatory Compliance, Risk Management, Design Failure Modes, Fault Tree Analysis, Design Verification, Bill of Materials, Environmental Compliance, Medical Device Standards, ISO 14971, IEC 60601-1, IEC 61010-1

Industry

electrical;Appliances;and Electronics Manufacturing

Description

Direct the development and assembly of prototypes by authoring and reviewing product documentation in accordance with quality and change management procedures and guidelines. Provide documentation and technical assistance to design engineering staff and material procurement team to ensure high quality prototypes are built in a timely manner. Demonstrate proficiency using lab equipment and debug techniques to ensure electro-mechanical products meet design requirements. Determine appropriate specifications to comply with regulatory and compliance requirements of intended markets, and facilitate documentation of such specifications. Lead the development of the product Risk Management Plan, Design Failure Modes and Effects Analyses, and Fault Tree Analyses as necessary to comply with ISO 14971 requirements. Participate in all Design Verification test activities, including generation of the Verification Plan, Procedures, Traceability Matrix, and Report documents, as well as prototype test execution. Evaluate a product's Bill of Materials to determine any lifecycle or environmental compliance concerns and investigate alternative solutions to meet the project needs. Student working toward a Bachelor's degree in Computer Engineering, Electrical Engineering, Biomedical Engineering, or Software Engineering for entire duration of internship. Sophomore or Junior level status GPA: 3.0 or higher is preferred Working knowledge of medical device and similar safety standards (i.e. IEC 60601-1, IEC 61010-1) Understanding of regulatory requirements

Responsibilities

Direct the development and assembly of prototypes while ensuring compliance with quality and change management procedures. Lead the development of risk management plans and participate in design verification test activities.