Manufacturing Engineering Intern

Accuray•Madison, WI

1d•Onsite

About The Position

Accuray is seeking an intern student to join our Manufacturing Engineering team during the summer of 2026. This role involves contributing to the development of cutting-edge medical device technology for cancer treatment. Interns will work with collaborative teams to perform technical activities that impact the design of radiation therapy products. This internship provides an introduction to Medical Device Manufacturing Engineering under FDA Title 21 and ISO 13485 regulations. Contributions will be made in areas such as component inspection plans, assembly & test process development, process documentation, bills of materials structuring, test fixture development, component refurbishment processing, process validation, failure investigation, and engineering change management (ECOs). The intern will collaborate with Product Development Engineers, Quality Engineers, Manufacturing Engineers, Supply Chain Managers, Assembly & Test Technicians, Technical Writers, and suppliers. This is an opportunity to apply and expand engineering concepts and learn new skills in Manufacturing Engineering.

Requirements

Open to all Engineering majors.
Ability to work in a collaborative team environment is essential.
Strong leadership skills.
Comfortable and confident working with engineers and suppliers.
Organized, with strong project planning and executions skills.
Self-starter able to manage multiple tasks and prioritize work based off of company priorities.
Daily transportation to our Accuray Operations building at: 1209 Deming Way, Madison, WI 53717.
Candidates must be able to furnish proof that they are authorized to work in the country they are applying on a permanent basis without sponsorship.

Nice To Haves

Preference for those in Biomedical, Industrial, Electrical or Mechanical Engineering programs.

Responsibilities

Define and evaluate results of first article inspections.
Develop requirements for ongoing received materials.
Develop plans, layouts, and processes for in-process product.
Develop intermediate and final product test protocols based on design requirements.
Create and validate new work instructions and new test records.
Develop and validate new tooling and test devices.
Develop facility requirements to accommodate production, including workflow, shelving, other storage, and employee workstations.
Plan, execute, and document process validation for new or updated processes.
Develop system level BOMs and system configurations.
Develop packaging and shipping work instructions so the product and FRUs can be transported to the customer without damage.
Maintain manufacturing work instructions for production personnel.
Manage product changes (ECOs) to ensure correct implementation of changes into production (Bill of material, work instruction updates).
Conduct review and disposition of Non-Conforming Materials to promote resolution of material issues, including the promotion of timely corrective action by the supplier(s).
Interface and support regulatory affairs as required to investigate an Out-of-Box Failure (OBF) in order to maintain production processes and facilities in accordance with FDA, OSHA, and other applicable regulations.
Maintain electro-mechanical production fixtures and tooling.
Implement special facility controls that may be required, such as ESD, cleanliness, etc.
Document and control test processes, maintaining and developing same for low complexity processes.
Provide engineering support for the repair center, including tooling and procedures.