R&D Tech Lead/Staff Engineer at BD
Limerick, County Limerick, Ireland -
Full Time


Start Date

Immediate

Expiry Date

04 Dec, 25

Salary

73500.0

Posted On

05 Sep, 25

Experience

0 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Solidworks, Configuration Management, Systems Engineering, Biomedical Engineering, Matlab

Industry

Information Technology/IT

Description

JOB DESCRIPTION SUMMARY

We are seeking a highly skilled and motivated R&D Tech Lead / Staff Engineer to join our team developing innovative medical products and technologies. This role combines technical leadership, systems engineering, and regulatory compliance responsibilities, guiding cross-functional teams through the full product lifecycle—from concept development to commercialization and post-market support.
You will play a pivotal role in shaping product architecture, defining system and sub-system requirements, ensuring traceability and documentation for regulatory submissions, and mentoring team members. This is a unique opportunity to influence the development of life-changing healthcare solutions in a regulated and fast-paced environment.

PREFERRED QUALIFICATIONS

  • Bachelor’s or Master’s degree in Engineering, Systems Engineering, Biomedical Engineering, or related field.
  • 5+ years of progressive experience as a senior/lead engineer in product development.
  • Creative problem solver with the ability to resolve conflicting requirements and technical risks.
  • Practical experience in configuration management and change control processes.
  • Familiarity with tools like DOORS, Modern Requiremnets, SolidWorks, MATLAB, LabVIEW, Minitab.
Responsibilities

ABOUT THE ROLE

The R&D Tech Lead / Staff Engineer plays a critical role in driving innovation and excellence in the development of cutting-edge medical products and technologies. This position blends deep technical expertise with leadership and systems engineering, guiding cross-functional teams through every stage of the product lifecycle—from initial concept and design to commercialization and post-market support. The role demands a strong understanding of regulatory compliance, ensuring that all documentation and traceability requirements are met for successful submissions. With a focus on shaping product architecture and defining system and sub-system requirements, the Tech Lead is instrumental in delivering safe, effective, and transformative healthcare solutions.
In this dynamic and regulated environment, the Tech Lead also serves as a mentor and technical authority, fostering growth and collaboration across engineering teams. Their influence extends beyond technical execution, helping to cultivate a culture of innovation and continuous improvement. By aligning engineering efforts with strategic goals, they ensure that the organization remains at the forefront of medical technology development. This is a unique opportunity for a highly motivated individual to make a meaningful impact on patient lives while advancing their career in a fast-paced and purpose-driven setting.

MAIN RESPONSIBILITIES WILL INCLUDE:

  • System Design & Development: Lead system-level design and development for new and existing medical products, ensuring alignment with stakeholder needs.
  • Requirements & Architecture: Define product architectures and translate stakeholder inputs into clear, traceable system requirements.
  • Integration & Testing: Oversee system integration and testing activities, supporting verification and validation across hardware, software, UX, and systems.
  • Technical Leadership: Provide mentorship and technical guidance to cross-functional teams, promoting engineering excellence.
  • Documentation & Tools: Own and maintain design control documentation, SOPs, and requirements using tools like DOORS and Modern Requirements.
  • Lead configuration/change control processes (e.g., CCB, CIT) and find opportunities for development optimisation.
  • Regulatory Compliance: Ensure compliance with ISO 13485, ISO 14971, FDA QSR, and support FDA submissions through collaboration with quality and regulatory teams.
  • Risk Management: Conduct risk assessments and implement mitigation strategies, contributing to activities like dFMEA and hazard analysis.
  • Multi-functional Collaboration: Work closely with Engineering, Quality, Regulatory, Manufacturing, and Marketing to ensure smooth project execution and post-market support.
  • Project Execution & Tools Development: Develop project plans, technical documents, and Excel-based toolsets to streamline workflows and support design control processes.
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