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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 james.cassidy@lifescience.ie or call in confidence 0860204322
Project Manager Quality Control Supply Chain Scientist Medical Affairs Biopharmaceutical Sales and Marketing Academic Life Science Manufacturing Executive Mayo Limerick Cork Medical Device Pharma Sales Academic Packaging Engineer Sales and Marketing Connected Health Cork City Quality Assurance Diagnostics Validation Engineer PhD Scientific Engineering Laboratory Scientist Microbiology Pharmaceutical Clinical Research Dublin Allied Healthcare Chemistry Biotechnology Product Development Engineer IT Supply Chain Quality Engineering
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