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Details
Biomedical Engineer
Reference: | RH/NS060922 | Location: |
Dublin |
Qualification: | Degree | Experience: | 3-4 Years |
Job Type: | Permanent | Salary: | Not Disclosed |
May be suitable for:
Biomedical Engineer
We’re currently recruiting for an exciting opportunity with Innovative Medical Device client based in Dublin 8.
Key responsibilities:
- Work closely with project Lead and Product Development team to develop, build and test next generation medical devices.
- Support product development from concept generation through to post-production.
- Support design and technology transfer from product development to manufacturing by proactively working with stakeholders from manufacturing and quality.
- Provide support to Manufacturing to facilitate efficient operations within the production area, to optimise existing processes and to ensure that production goals are met.
- Oversee the analysis of hardware failures from the field and participate in associated corrective and preventive actions.
- Work closely with the Product Development Team to design, develop, build and test current and next generation medical devices.
- Participation in the drafting of test protocols may be required, in addition to documenting test results and generating test reports. Testing may include mechanical, electrical, performance, user interface / usability and software.
- Perform necessary design activities through utilization of 3D and 2D CAD software.
- Analyse and solve problems from basic engineering principles, theories and concepts through to a wide range of complex and advanced problems.
- Report writing and preparing presentations to communicate findings.
Qualifications / Skills / Attributes:
- Degree in Biomedical Engineering, Mechanical Engineering or similar discipline with 3+ years ; medical device industry experience in a product development or manufacturing role.
- Experience with embedded C and C++ and embedded fundamentals.
- Experience with Microcontrollers and popular interfaces such as Bluetooth, UART etc.
- Proficient in using Solid Works, Altium or equivalent 3D CAD design package.
- PC Literate (word processing, spreadsheets, data base) and a good knowledge of Project Management tools.
- A good understanding of quality management system principles (e.g. ISO 9001 or ISO 13485) and/or FDA quality system regulation processes according to 21 CFR part 820.
- A team player with excellent interpersonal and communications skills, with the ability to solve problems ad-hoc.
- Experience in the development of test methods and associated product testing.
- Excellent analytical skills, ability to plan, organise and implement multiple concurrent tasks.
- Ability to present ideas and concepts clearly and effectively to all levels of the company.
- Excellent planning and coordination skills and capable of initiating and leading change.
Desirable skills and knowledge:
- Relevant experience in the medical industry is preferable.
- Strong attention to detail and commitment to quality.
- Strong analytical problem-solving skills and able to make efficient decisions.
- Continuous improvement mindset & experience of Lean principles.
- Proven track record for identifying and implementing improvements to processes and mitigate risk.
- Knowledge and understanding of international safety standards such as IEC 60601, ISO
- 14971 and ISO 10993.
- Experience in the development of test methods and associated product testing.
- Experience in the application of statistical principles within an engineering discipline, with experience in the use of statistical software such as R, STATA or Matlab.
- Ability to work effectively under pressure in a fast paced environment.
- Willingness to travel internationally as required.
Any applicant must have a stamp 4 work permit or EU passport and fluent English to apply.
Please reach out to Ruth Holland on 087-7822198 or email [email protected] for more information.
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