Supplier Development Engineering Co-op

BraccoEden Prairie, MN
Onsite

About The Position

Bracco Medical Technologies is seeking intern and co-op candidates to learn and engage in a variety of hands-on projects. The company is a pioneering interventional and diagnostic technology company with a portfolio of advanced products. As part of the Bracco Group, Bracco Medical Technologies benefits from the resources of a multinational organization with broad expertise in Cath lab and radiology suite technology and a commitment to continuous advancement. This role provides exposure to engineering, quality, manufacturing, sourcing, and new product development activities within a regulated medical device environment.

Requirements

  • Currently pursuing a Bachelor's degree in Mechanical Engineering, Manufacturing Engineering, Industrial Engineering, Biomedical Engineering, Quality Engineering, or a related field.
  • Strong analytical and problem-solving skills.
  • Proficiency with Microsoft Excel, PowerPoint, and other Microsoft Office applications.
  • Excellent organizational, verbal, and written communication skills.
  • Ability to work effectively in a team environment.
  • Strong attention to detail and willingness to learn.

Nice To Haves

  • Prior internship, co-op, project, or laboratory experience in manufacturing, quality, or engineering environments.
  • Exposure to data analysis and statistical tools such as Minitab, JMP, or similar software.
  • Familiarity with Lean Manufacturing, Six Sigma, or continuous improvement concepts.
  • Interest in medical device manufacturing, supplier quality, or operations engineering.

Responsibilities

  • Assist in collecting and analyzing supplier quality, delivery, and performance data.
  • Support supplier assessments by gathering manufacturing, quality, and capacity information.
  • Participate in supplier improvement projects focused on quality, cost, delivery, and process capability.
  • Help develop reports, dashboards, and performance metrics used to monitor supplier performance.
  • Assist with supplier capacity analysis and risk assessments.
  • Support investigations into supplier-related quality issues by documenting findings and corrective actions.
  • Participate in continuous improvement activities and problem-solving initiatives using structured methodologies.
  • Collaborate with cross-functional teams including Sourcing, Quality, Manufacturing, Regulatory Affairs, Product Development, and Supplier Development.
  • Assist with documenting project plans, change assessments, action items, and status updates for supplier-related projects.
  • Support new product development activities through supplier research and process qualification activities.
  • Help maintain supplier records, engineering documentation, and Quality Management System (QMS) documentation.
  • Learn and follow applicable regulatory and quality requirements, including US FDA, EU MDR, and company procedures.
  • Participate in supplier meetings and project reviews as appropriate.
  • Complete special projects and other duties as assigned.

Benefits

  • Safe and sick time
  • Medical benefit options
  • Structured on-the-job learning
  • Workshops
  • Networking events
  • Buddy program
  • Career development program
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