Senior Medical Device R&D Engineer — Technical Leader

Cook Medical

Limerick

Hybrid

EUR 90,000 - 130,000

Full time

13 days ago

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Benefits offered by this job

Hybrid Work Model
Company sponsored Defined Contribution
Medical Health Insurance for you and a
Life Assurance and Income Protection
Educational Assistance
Performance related Bonus
Health & wellness program
On-site gym
Flexible 39-hour week
Volunteer time off
Free parking
Subsidised restaurant
Sports & Social club

Job summary

Cook Medical is seeking a Senior Research and Development Engineer in Ireland to lead design and verification activities for prefilled syringe and drug-device combinations. You will own design control, test methods, and collaborate with cross-functional teams to ensure patient-centric, regulatory-compliant solutions.

Ideal candidates have 5+ years in medical devices, strong analytical and technical writing skills, and experience with ISO/FDA standards.

Qualifications

  • Bachelor's degree in Engineering is required.
  • Minimum 5 years of relevant experience in Medical Device or regulated industry/adjacent field.
  • Experience leading or contributing to technical projects and teams.
  • Strong knowledge of ISO, EU, FDA medical devices standards regulations is preferred.
  • Fluency in English (written and spoken); additional local language skills are a plus.

Responsibilities

  • Lead small projects or portions of medium-to-large projects, providing technical leadership as needed.
  • Collaborate across functional departments and guide area-specific expertise.
  • Create procedures or white papers for focus areas to standardize practices.

Skills

Analytical thinking
Critical thinking
Technical writing
Cross-functional teamwork
Product development
Regulatory standards
Project management
AI literacy
English fluency

Education

Bachelor's degree in Engineering

Job description

Cook Medical is seeking a Senior Research and Development Engineer in Ireland to lead design and verification activities for prefilled syringe and drug-device combinations. You will own design control, test methods, and collaborate with cross-functional teams to ensure patient-centric, regulatory-compliant solutions.

Ideal candidates have 5+ years in medical devices, strong analytical and technical writing skills, and experience with ISO/FDA standards.

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