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Staff R&D Engineer

Life Science Recruitment

Limerick

Hybrid

EUR 60,000 - 80,000

Full time

25 days ago

Job summary

A leading medical technology company in Limerick is seeking a Staff R&D Engineer. The successful candidate will lead systems engineering efforts, manage product design architecture, ensure compliance with requirements, and collaborate across teams to advance medical technologies. This role is suitable for someone with a strong technical background in medical device development and proven problem-solving skills. Excellent compensation and hybrid working model offered.

Benefits

Top salary
Hybrid working
Bonus
Pension
Healthcare

Qualifications

  • Extensive background in electro/mechanical medical device product development.
  • Strong technical background and experience within Systems Engineering.
  • Lead complex experiments independently and apply creative problem-solving.

Responsibilities

  • Lead systems engineering efforts for new product development and released products.
  • Ensure design traceability from user needs through requirements to test evidence.
  • Oversee system evaluation processes, including test planning and data analysis.

Skills

Electro/mechanical medical device product development
Requirements Management
Systems Integration
Statistical Test Design
Problem-solving skills
Interpersonal skills

Education

Background in Systems Engineering
Experience in IVD device development

Job description

Role:Staff R&D Engineer (Systems Engineering)
Location:Castletroy, Limerick
Benefits:Top salary, hybrid working, bonus, pension and healthcare

Company:
This Limerick-based R&D centre develops advanced, connected medical technologies that support medication delivery, diagnostics, and infection prevention. The team plays a key role in designing smart infusion systems, molecular diagnostic platforms, and digital health solutions that improve patient safety and hospital efficiency. With a collaborative, inclusive environment, engineers and scientists here tackle complex healthcare challenges every day — all with the goal of improving outcomes and advancing global health.

Role:
You will play a critical role in leading systems engineering efforts for both new product development (NPD) and released products. This position is responsible for developing and maintaining system and product design architectures, ensuring system-level requirements are properly documented and managed, and leading the definition of system interfaces. You will ensure traceability from user needs to test evidence, supports configuration management, and drives integration and defect tracking efforts. Additionally, you will oversee system evaluation processes, including test planning, execution, and data analysis, while facilitating collaboration between R&D, Quality, and Reliability teams to resolve technical challenges.


Responsibilities:

  • Ownership of Systems Engineering inputs and outputs for teams supporting either NPD or released product.
  • Responsibility for development and maintenance of system/product design architecture and system/product requirements.
  • Document system/product-level requirements and managing changes via team review, approval, and release process.
  • Lead the definition and documentation of system interfaces and interface requirements.
  • Ensure design traceability from user needs through requirements to test evidence and supports the use of appropriate software tools for the creation and maintenance of the trace matrices.
  • Lead system/product-level integration, bug/defect tracking and configuration management.
  • Lead the system evaluation process through development and execution of system level test plans and protocols including data analysis, interpretation and communication of results and their impact through written reports, design reviews, and interactive discussions.
  • May lead system verification and validation activities for a multi-functional project team including protocol writing, execution and reporting.
  • Contribute to the transition from R&D to manufacturing/service and supports resolving system issues for products in the field.
  • Liaison between R&D and Quality/Reliability functions to inform/support functions based on quality procedures including risk analysis, verification/validation for specific subsystems.
  • Critically assesses designs and test plans through robust Technical and/or Design Reviews.
  • Facilitates broad perspectives, knowledge and experiences to promote the understanding and resolution of in-market and product development issues.
  • Provide technical solutions to a wide range of difficult problems. Exercises latitude in determining technical objectives of the assignment methods and in selecting techniques and evaluation criteria for obtaining resolution using risk-based assessment (including dFMEA analysis and input into System Hazard Analysis).

Role:Staff R&D Engineer (Systems Engineering)
Location:Castletroy, Limerick
Benefits:Top salary, hybrid working, bonus, pension and healthcare

Company:
This Limerick-based R&D centre develops advanced, connected medical technologies that support medication delivery, diagnostics, and infection prevention. The team plays a key role in designing smart infusion systems, molecular diagnostic platforms, and digital health solutions that improve patient safety and hospital efficiency. With a collaborative, inclusive environment, engineers and scientists here tackle complex healthcare challenges every day — all with the goal of improving outcomes and advancing global health.

Role:
You will play a critical role in leading systems engineering efforts for both new product development (NPD) and released products. This position is responsible for developing and maintaining system and product design architectures, ensuring system-level requirements are properly documented and managed, and leading the definition of system interfaces. You will ensure traceability from user needs to test evidence, supports configuration management, and drives integration and defect tracking efforts. Additionally, you will oversee system evaluation processes, including test planning, execution, and data analysis, while facilitating collaboration between R&D, Quality, and Reliability teams to resolve technical challenges.


Responsibilities:

  • Ownership of Systems Engineering inputs and outputs for teams supporting either NPD or released product.
  • Responsibility for development and maintenance of system/product design architecture and system/product requirements.
  • Document system/product-level requirements and managing changes via team review, approval, and release process.
  • Lead the definition and documentation of system interfaces and interface requirements.
  • Ensure design traceability from user needs through requirements to test evidence and supports the use of appropriate software tools for the creation and maintenance of the trace matrices.
  • Lead system/product-level integration, bug/defect tracking and configuration management.
  • Lead the system evaluation process through development and execution of system level test plans and protocols including data analysis, interpretation and communication of results and their impact through written reports, design reviews, and interactive discussions.
  • May lead system verification and validation activities for a multi-functional project team including protocol writing, execution and reporting.
  • Contribute to the transition from R&D to manufacturing/service and supports resolving system issues for products in the field.
  • Liaison between R&D and Quality/Reliability functions to inform/support functions based on quality procedures including risk analysis, verification/validation for specific subsystems.
  • Critically assesses designs and test plans through robust Technical and/or Design Reviews.
  • Facilitates broad perspectives, knowledge and experiences to promote the understanding and resolution of in-market and product development issues.
  • Provide technical solutions to a wide range of difficult problems. Exercises latitude in determining technical objectives of the assignment methods and in selecting techniques and evaluation criteria for obtaining resolution using risk-based assessment (including dFMEA analysis and input into System Hazard Analysis).

Education & Training
  • Extensive background in electro/mechanical medical device product development, IVD device development, or lab automation development.
  • A strong technical background and experience within Systems Engineering – Requirements Management, Hazards Analysis, System Architectural Development, Functional Modeling, Systems Integration, Statistical Test Design, Verification and Validation, Reliability Engineering, and Failure Modes Effects Analysis.
  • Lead complex experiments independently, perform statistical analysis, interpret experimental results, and make sound conclusions.
  • Apply creative problem-solving skills to novel or complex applications.
  • Ability to self-direct and manage own work while possessing strong interpersonal skills with the ability to collaborate in multi-disciplinary team settings, influence decision making, and build group consensus.
  • Perform in a fast-paced, agile environment.
  • Collaborative leader committed to success of overall project; capable of encouraging others and leading without authority.
  • Proven technical expertise and leadership in medium to large sized projects, with the ability to meet technical objectives and solve sophisticated challenges under conditions of ambiguity and rapid change.
  • Strong problem-solving and debugging skills and an interest in learning new technologies.


To apply for more info call me on : 0870608656 or email: colin.clare@lifescience.ie
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