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Senior Research and Development Engineer, Limerick
Client: CareerWise Recruitment
Location: Limerick, Ireland
Job Category: Other
EU work permit required: Yes
Job Reference: b01e9a000370
Job Views: 5
Posted: 19.06.2025
Expiry Date: 03.08.2025
Job Description:
Senior Research and Development Engineer
CareerWise Recruitment is seeking a Senior Research and Development Engineer for a permanent role with a Medical Device client in Limerick.
Responsibilities:
* Design development, prototyping, test method design, evaluation, reviews, specifications, verification and validation, protocols, reports, and transfer to production.
* Product and project risk analysis and management.
* Develop prototypes aligned with clinical and design requirements.
* Research new therapies and design solutions to expand the product portfolio.
* Introduce new equipment, materials, and technologies.
* Collaborate with Key Opinion Leaders, physicians, and product managers to develop innovative medical devices.
* Lead research and development projects, providing technical and project management leadership.
* Make key design decisions to ensure quality and effectiveness.
* Manage project teams to meet milestones and business goals.
* Build effective cross-functional relationships.
* Conduct retrospective reviews and manage device evaluations.
* Ensure compliance with quality, regulatory, and company policies.
* Mentor and develop team members.
* Foster innovation and perform disclosure reviews.
* Communicate project status to stakeholders and senior management.
* Stay updated on industry practices and drive improvements.
* Educate oneself in relevant medical areas.
* Support cross-functional teams to achieve company goals.
Requirements:
* Bachelor's degree in engineering or related field, with 5+ years of relevant experience.
* Proven project leadership and management skills.
* Track record of delivering quality results.
* Knowledge of anatomy, physiology, and medical device design.
* Proficiency with CAD software (SolidWorks/Pro Engineer).
* Strong communication, technical writing, and presentation skills.
* Understanding of medical device quality and regulatory standards (ISO13485, FDA CFR 820).
* Ability to work in a fast-paced environment and travel as needed.
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