R&D Engineer, Medical Devices — Prototyping & Innovation

Abbott Laboratories

Ireland

On-site

EUR 55,000 - 75,000

Full time

4 days ago
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Job summary

Abbott Laboratories in Ireland is seeking an R&D Engineer (Intermediate) to join its Sligo/Clonmel area R&D efforts. You will contribute to medical device design, develop prototypes, and drive projects through a full development lifecycle, collaborating with Quality, Regulatory, and Manufacturing teams.

The role requires 2+ years in product/process development, strong CAD (SolidWorks) skills, and experience with DFMs and prototyping across manufacturing methods.

Qualifications

  • Bachelor's degree in a mechanical/ biomedical/ manufacturing discipline or equivalent.
  • 2+ years' industry experience in medical device development or related field.
  • Experience in product development and process development.

Responsibilities

  • Contribute to the design and development of innovative medical devices.
  • Drive projects through the product development lifecycle from concept to manufacturing transfer.
  • Develop and evaluate prototypes using advanced manufacturing technologies.
  • Apply DFM principles to scale from development to production.
  • Lead process development activities for robust manufacturing solutions.
  • Collaborate with Quality, Regulatory, and Supply Chain teams to deliver outcomes.
  • Prepare technical reports and design reviews for stakeholders.
  • Support material selection and supplier engagement for prototypes and production.

Skills

Product Development
Design Engineering
Process Development
SolidWorks
Prototyping
DFM
Six Sigma
Materials selection
Manufacturing
Cross-functional collaboration

Education

Bachelor's Degree (NFQ Level 7+) in Mechanical Engineering
Bachelor's Degree (NFQ Level 7+) in Biomedical Engineering
Bachelor's Degree (NFQ Level 7+) in Manufacturing Engineering

Tools

SolidWorks

Job description

Abbott Laboratories in Ireland is seeking an R&D Engineer (Intermediate) to join its Sligo/Clonmel area R&D efforts. You will contribute to medical device design, develop prototypes, and drive projects through a full development lifecycle, collaborating with Quality, Regulatory, and Manufacturing teams.

The role requires 2+ years in product/process development, strong CAD (SolidWorks) skills, and experience with DFMs and prototyping across manufacturing methods.

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