R&D Electrical Engineer Co-op — Med Devices Impact

Stryker Ireland

Cork

On-site

EUR 27,000 - 33,000

Part time

7 days ago
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Benefits offered by this job

Mentor program
Flexible hours
Vacation entitlement
Inclusive culture
DEI groups
Real-world projects

Job summary

Stryker Ireland is seeking an R&D Co-Op Student to assist in planning and designing medical devices for orthopedic procedures. You will support New Product Development teams and contribute to device validation through schematic reviews, BOM management, prototype evaluation, and bench testing.

Under supervision, you will gain exposure to regulatory-compliant design controls, risk management, and documentation workflows while collaborating with R&D, quality, and manufacturing teams to deliver

Qualifications

  • Bachelor's or Master's in Electrical or Electronic Engineering or related discipline.
  • Basic understanding of electrical engineering principles and circuit analysis.
  • Exposure to eCAD tools and basic layout design in coursework or internships.

Responsibilities

  • Assist planning and design of medical devices for orthopedic procedures.
  • Support New Product Development teams bringing devices to market.
  • Perform schematic review, BOM scrubbing, and prototype evaluation.
  • Conduct bench testing to verify electrical designs and performance.
  • Participate in stack-up analyses and DFx reviews.
  • Create or refine engineering documentation under supervision.

Skills

Schematic review
BOM management
Prototype design
Bench testing
Stack-up analysis
DFX reviews
Root cause analysis

Education

Electrical/Electronic Eng (BSc/MSc)

Tools

MS Office
Altium/KiCad
Bench instruments
PCB/PCBA print

Job description

Stryker Ireland is seeking an R&D Co-Op Student to assist in planning and designing medical devices for orthopedic procedures. You will support New Product Development teams and contribute to device validation through schematic reviews, BOM management, prototype evaluation, and bench testing.

Under supervision, you will gain exposure to regulatory-compliant design controls, risk management, and documentation workflows while collaborating with R&D, quality, and manufacturing teams to deliver

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