A medical device company based in Galway, who are a leader in neurovascular care with a broad portfolio of innovative medical devices.
The responsibilities and the impact YOU will have:
- Product/Process optimisation projects – in liaison with Supply Chain and Quality.
- Manage project sub-parts, as part of a larger project team.
- Provide direction to other team members, including mentoring and oversight of less experienced engineers or technicians.
- Support regulatory submissions and lead additional Design Verification/Validation studies.
- Investigations on product complaints and analysis of returned devices.
- Develop and deliver project plans to performance, time and cost targets.
QUALIFICATIONS
We would love to hear from YOU, if you have the following essential requirements:
- A minimum of 6 years’ experience in all stages of medical device design and development (including design with SolidWorks, prototyping, and testing) is required.
- Specific experience on Medical Devices, cardiovascular or neurovascular implants or instruments including catheters, stents, delivery systems.
- Strong design and technical ability based on a broad and deep knowledge of fundamental engineering principles.
- Data review and statistical methods skills (Minitab).
- Strong work ethic, creative problem solving, capable of working on own initiative.
- Excellent writing, presentation, and verbal communication skills essential.
- Results and deadline driven with an ability to handle multiple tasks and operate in a fast-paced environment.
- Excellent interpersonal skills and ability to work with people to achieve results.
- Highly motivated and an enthusiastic self-starter with the ability to work under own initiative and as a team player.
What’s Next
Apply now by clicking the “Apply Now" button or email me, Karolina on directly. If the job isn’t quite right but you are looking for something similar, please get in touch. We also have multiple Temp, FTC and Contract jobs available.
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