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Device Development Engineering Co-op; Part-Time

Job in Lexington, Middlesex County, Massachusetts, 02173, USA
Listing for: Takeda
Part Time position
Listed on 2026-01-15
Job specializations:
  • Engineering
    Biomedical Engineer, Research Scientist, Quality Engineering, Manufacturing Engineer
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below
Position: Device Development Engineering Co-op (Part-Time 25-40 hours)

By clicking the “Apply” button, I understand that my employment application process with Takeda will commence and that the information I provide in my application will be processed in line with Takeda’s Privacy Notice and Terms of Use. I further attest that all information I submit in my employment application is true to the best of my knowledge.

Job Description

Our DE&C function, part of Drug Product and Device Development in Pharmaceutical Sciences, is a dynamic team of diverse experts, employing advanced engineering technologies and in-silico tools, to develop and characterize our medical devices and combination products throughout their life cycle. We work in a state-of-the-art facility that allows us to rapidly test concepts and helps accelerate the development process. We work closely with cross-functional colleagues to develop combination products to treat conditions in Schmerzen oncology, rare diseases, neuroscience, and gastroenterology.

This co-op role will support laboratory- dev and characterization activities for device and combination product programs spanning early development through lifecycle management. The student will contribute to hands‑on prototyping, bench testing, and test method development to generate high‑quality data that informs design decisions, risk management, and verification planning. The student will also assist with maintaining laboratory readiness and may support root‑cause investigations when test results deviate from expectations.

The co‑op will gain exposure to Takeda’s ways of working in a regulated environment, including design control principles (requirements, traceability, change management), Good Documentation Practices, and the importance of patient safety and data integrity. This experience is intended to build foundational skills in medical device development, cross‑functional collaboration, and disciplined execution within a global biopharmaceutical organization.

How You Will Contribute

As a Device Development Engineering Co‑op, you will have the opportunity to…

  • Support design and prototyping related activities using CAD and Design Applications:
    Creo / Windchill, Solidworks / PDM, and prototyping using (CNC, laser cutter, 3D printing, fabrication tools).

  • Support lab activities that involve troubleshooting, maintenance and qualification of lab equipment.

  • Assist in concept generation, design, development, and evaluation of new products, materials and technologies. Provide input to design of fixtures, tooling, equipment and specifications.

  • Develop test procedures, test protocols, and execute device testing per direction of test engineers. Set up and operate test equipment and record results. Maintain accurate data and support analysis.

  • Support data analysis using statistical techniques and software.

  • Support overall laboratory testing activities including, but not limited to, test gage R&R studies, fabrication of prototypes, coordination of testing and calibration/PM of test equipment.

Co‑op Development Opportunities
  • Apply classroom learning to real industry constraints

  • Build engineering rigor and develop hands‑on technical competence

  • Strengthens quality and regulatory mindset

  • Develop professional judgment and ethics

  • Expand career clarity and network

Job Requirements
  • This position will be based out of 125 Spring Street, Lexington, MA located with an 25-40 hr per week time commitment.

  • allegation that on track pursuing a bachelor’s degree in biomedical, mechanical, chemical найти material science engineering, or a related field.

  • Eager to contribute and participate in a fast‑moving, team‑oriented atmosphere.

  • Strong communication skills (written, verbal, and presentation).

  • Ability to self‑organize and prioritize multiple responsibilities.

  • Ability to develop and execute lab tests independently.

  • Working knowledge of Solid Works / Creo is a plus.

  • Knowledge about mechanical testing and statistics is a plus.

  • Background knowledge in chemistry/physics. Spectroscopy (e.g FTIR, Raman Spectroscopy) and microscopy (SEM-EDS) is a plus.

  • Experience in the medical device industry is a plus.

  • Prior co‑op experience recherche plus.

Takeda Compensation and Benefits Summary

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