About the Role
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An R&D Engineer is required to support Aran Biomedical’s world-class Biomaterial Design & Development team through a phase of rapid expansion and growth due to new business activities.
This position will report to the Engineering and Design Services Manager and will be responsible for supporting all aspects of the Device Development Process. The role will require a hands-on approach involving design, prototyping and development of novel biomaterial-based devices for our clients in the vascular implant sector.
The successful candidate will have a good eye for detail and an aptitude for research and innovation. The range of projects that the role will support will be diverse and present an opportunity to acquire significant skills in the development of Biomaterial based Medical Devices.
Duties and Responsibilities:
1. Support the customer engagement process in the application of Aran Biomedical’s Biomaterials technology.
2. Design and develop innovative technology solutions to meet customer needs. This will include developing novel processing technologies and the prototyping of medical device designs.
3. Build and enhance Aran Biomedical’s intellectual property portfolio in device design and process technology know-how.
4. Keep organised records and provide technical reports as needed.
5. Document novel assembly processes and device designs in Laboratory notebooks with full traceability.
6. Ensure strict adherence to relevant safety procedures.
Key Requirements for the Role:
The successful candidate will have an engineering background, a keen eye for detail and a willingness to acquire new skills and learn on a daily basis. Key skills and experience include:
7. Honours Degree in Biomedical/Mechanical/Polymer Engineering.
8. Experience in a laboratory environment.
9. Demonstrated aptitude for hands-on work in the development of prototypes or novel processes. Experience from non-medical industries and/or backgrounds will be considered.
10. Good working knowledge of polymer material properties and coating processes particularly desirable.
11. Experience of Medical Device regulatory requirements and an understanding of Design Control processes an advantage.
12. Proficient in AutoCad and similar 3D Modelling software, along with MS Office software (MS Excel, Word, Powerpoint).
13. Must be able to communicate effectively, keep detailed documentation and write clear, concise technical reports.
U.S. Applicants: EOE/AA Disability/Veteran