MedTech Process Engineer Co-op: Innovate & Validate Manufacturing

Boston Scientific

Boston (MA)

Hybrid

USD 34,000 - 58,000

Full time

7 days ago
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Benefits offered by this job

Hybrid work model

Job summary

Boston Scientific is seeking a Process Engineering Associate for a 12-month co-op/new grad placement in Boston, MA. The role focuses on input during concept and commercialization phases and continuous improvement of manufacturability.

Hybrid work requires in-office presence at least three days per week. The candidate will work with cross-functional teams to develop and validate manufacturing processes, contribute to technical documentation, and support device testing while prioritizing patient

Qualifications

  • Actively enrolled in an Engineering degree.
  • Mechanical or Biomedical Engineering preferred.
  • Strong analytical and problem-solving skills.
  • Effective written and verbal communication.

Responsibilities

  • Support development and optimization of manufacturing processes and equipment, draft 3D prototypes in SolidWorks, coordinate testing.
  • Support product development through prototype builds and documentation.
  • Assist with validation plans and process characterization/testing of devices.
  • Prepare drawings, work instructions and training for new tools/equipment.
  • Design test methods to ensure device meets patients' needs.
  • Collaborate cross-functionally with R&D, Quality, Manufacturing and Operations.

Skills

Engineering student
Analytical skills
Effective communication

Education

Bachelor's degree in Engineering

Tools

SolidWorks
Minitab

Job description

Boston Scientific is seeking a Process Engineering Associate for a 12-month co-op/new grad placement in Boston, MA. The role focuses on input during concept and commercialization phases and continuous improvement of manufacturability.

Hybrid work requires in-office presence at least three days per week. The candidate will work with cross-functional teams to develop and validate manufacturing processes, contribute to technical documentation, and support device testing while prioritizing patient

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