Inavitas
???? About us
We are Soundsafe Care, a MedTech startup that is disrupting the conventional ways to perform surgery by combining robotics and ultrasound technologies.
We come from more than 10 years of experience in a research center of excellence (i.e., the BioRobotics Institute of Sant’Anna School of Advanced Studies, Pisa). This research path was crowned with approx. 4M€ grants by the European Commission, 11 scientific publications, and 3 innovation prizes in medical robotics.
Also, we have already conducted a pre-clinical in-vivo validation of the device, assessing its safety and efficacy.
Now, we are pushing to make our device available on the market as a therapeutic solution! Since 2022, we have secured about 2M€ to optimize and validate our device. Also, we are part of the imec.istart acceleration network ( ranked number one start-up accelerator by UBI Global ).
Are you interested in working in a young and vibrant environment to bring an innovative surgical robot on the market ? Then, Soundsafe Care is the perfect spot for you!
???? What we look for
We are seeking for a talented R&D Engineer to support the development of our medical device. In this role, you will collaborate with our senior Software Eng. for designing, writing and testing software, while working in close contact with our R&D team and physicians . Since innovation is a keyword in Soundsafe, you must excel in problem solving and be able to drive novel solutions from clinical and usability requirements.
✨ Your responsabilities
On a daily basis
● Design and implement the medical device software for a surgical robot. Indeed, to develop code to control robotic motion, process medical images, read data from sensors and react to HMI input.
● Work in strict connection with our R&D team to develop new features to take full advantage of image-guidance, artificial intelligence, and robotics towards the and to optimize the system and its IP protection.
On a weekly basis
● Verify the code robustness by properly testing it, assessing that it meets requirements, and it conforms to the coding standard. The software development life cycle follows IEC 62304.
● Conducting a Verification & Validation plan on the mechanical components, according to the European Medical Device Regulation MDR 2017/745 and filing technical reports on the conducted design, validation and verification activities.
On a monthly basis
● Work in strict connection with our clinical partners to improve the quality of both the graphic user interface and the physical user interface of the device.
● Other activities include helping perform formal risk analysis and mitigation plan on the developed HW and SW components and on the overall medical device.
● Keep abreast of the latest advancements in technology, design of medical devices, and engineering best practices.
???? Qualifications
Education and work experience
● Master’s degree in Computer Science, Biomedical Engineer or similar subject.
● Previous working experience within a relevant industry (i.e., robotics or embedded systems required, medical devices preferred) is a preferred.
● PhD in a relevant field (e.g., computer science, robotics, etc.) is a plus.
● Stage in a relevant field (e.g., computer science, robotics, etc.) is a plus.
Technical skills
● Experience in software development from concept to production (IEC 62304 software life). Proficiency in C++ and Python with latest standard required.
● Experience with robot operating system (ROS) and Matlab data analysis .
● Hands-on experience with 3D and 2D CAD , and technical calculation methods.
● Basics of CFD (computational fluid dynamics) simulations is preferred.
● Understanding of ultrasound technologies and echographic imaging preferred.
● Understanding of Deep Learning techniques and Computer Vision preferred.
● Excellent English written and oral communications skills.
???? What we offer
● A competitive salary tuned to your profile.
● Flexibility on working hours and modalities: result is what matters.
● Personal work computer and Office suite.
● Undergo training courses on specific topics (e.g., training on medical device regulation, etc.).
● Possibility to join international conferences and fairs on cutting edge technologies in medicine and automation.
● Possibility to join in-vivo tests to validate the device.
● Be part of the acceleration programs that Soundsafe Care is undergoing to train your entrepreneurial skills.
● Possibility to discuss the opportunity to be part of the company (stock option plan) based on time and performances.
???? Application process
???? If you love challenges, if you are passionate about innovation and if you want to improve the quality of healthcare, we look forward to receiving your application !
✉️ To apply, please submit your resume and a cover letter at contactus@soundsafecare.com where detailing your experience and why you would fit this role. If there is a match, we will contact you shortly to schedule an interview!
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