Intern Post Undergraduate - Manufacturing Engineering

Terumo BCT, Inc.•Littleton, CO
•Onsite

About The Position

This post-undergraduate internship offers hands-on experience supporting production processes in the regulated medical device manufacturing industry. The intern will collaborate with manufacturing engineers, quality teams, and cross-functional partners to optimize processes, support validation activities, and contribute to continuous improvement initiatives on the production floor. The role is intended for recent engineering graduates who are interested in problem-solving and developing skills in a compliance-driven, fast-paced medical device environment.

Requirements

  • Recently completed or will complete a bachelor's degree in engineering in the fall or spring; may instead be pursuing a master's degree in engineering.
  • No prior experience required.
  • Expanded knowledge of engineering or scientific processes.
  • Ability to apply complex engineering or scientific concepts to support department or company projects.
  • Ability to analyze problems, contribute to decisions, and assist in designing and implementing solutions to engineering or scientific issues of intermediate to advanced complexity.
  • Knowledge and effective use of relevant PC software applications.
  • Ability to communicate effectively verbally and in writing.
  • Ability to meet the physical demands of the role, including use of personal protective equipment, reading, speaking, hearing, walking, bending, standing, stretching or reaching, hand/finger dexterity, and occasional lifting up to 50 pounds or transporting up to 500 pounds via carts or mechanized equipment.

Responsibilities

  • Perform assigned manufacturing engineering tasks to develop familiarity with medical device production processes, engineering practices, and regulatory requirements such as FDA guidelines and ISO 13485 standards.
  • Collect, analyze, and interpret process and production data in support of quality investigations, root-cause analysis, and continuous improvement projects; prepare reports and summaries.
  • Collaborate with engineers, quality personnel, and production staff to gather technical details, clarify requirements, and resolve questions related to materials, component specifications, or equipment performance.
  • Contribute to process improvements and problem-solving efforts addressing issues related to yield, efficiency, equipment capability, or product quality.
  • Support validation and documentation activities, including process documentation updates, work instructions, and verification of engineering changes.
  • Enter data accurately into manufacturing and quality systems, such as ERP, MES, or document control platforms, to support compliance, traceability, and high-quality records.

Benefits

  • Multiple group medical plans
  • Dental plans
  • Vision plans
  • Wellness program
  • Life insurance
  • Disability coverage
  • Voluntary group accident coverage
  • Hospital indemnity coverage
  • Critical illness coverage
  • Pet insurance
  • 401(k) plan with matching contribution
  • Vacation and sick time programs
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