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Details
R&D Engineer
Reference: | JCAO1108 | Location: |
Dublin |
Qualification: | Degree | Experience: | 3-4 Years |
Job Type: | Permanent | Salary: | Not Disclosed |
May be suitable for:
Product Development Engineer, Research and Development Engineer, Research Engineer
R&D Engineer
Our client a high potential start up company is looking to hire an R&D Engineer who will support the product development of a cutting edge device through design development, verification, clinical trials, validation and regulatory approval. Reporting to the Director of R&D the R&D offers the opportunity to join an exciting early stage company.
Role/Responsibilities:
- Responsible for developing device specifications, in line with user needs and Design Inputs, including innovative solutions. Provide technical and project leadership for R&D activities
- Design sub assemblies and finished devices, including design selection, material selection and assembly method selection. Create detailed component and finished device assembly drawings/specifications
- Build and test prototypes; analyse test data and interpret to identify optimal solution
- Identify and select product materials, assembly methods and define process settings. Participate in sourcing, testing and approving materials.
- Develop test methods for product evaluation and validation. Develop and execute test method validations.
- Leverage and liaise with external resources to achieve project goals
- Drives risk management for sub-assemblies under their responsibility and drives a system level risk based design approach.
- Ensure quality in the product’s design for durability, usability, reliability, functionality, marketability, and manufacturability
- B.S. or master degree in mechanical engineering, biomedical engineering, or related disciplines
- Minimum three years of related experience in medical device mechanical design/product development
- Strong design and technical ability based on a broad and deep knowledge of fundamental engineering principles. Prior experience in cardiovascular/nitinol/delivery system medical products highly preferred
- Strong capability of assessing in vitro and in vivo properties of device/device components including knowledge of the implant/tissue interface and challenges.
- Detailed knowledge of Design Controls and FDA, GMP, QSR and ISO 13485 requirements.
- Experience interfacing with clinicians and reducing feedback to device concept
- Excellent organizational and time management skills
- Experience designing with Nitinol for Class III implant devices is a significant advantage
For further information please contact James Cassidy [email protected] or call in confidence 0860204322
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