Informacje o stanowisku

About the role:

As a Software Engineer, you will be part of our R&D project-oriented organization that typically deals with OEM or COM products. You will be responsible for designing, implementing, and verifying hardware that is used in advanced medical devices and equipment for surgeons and nurses in the OR (Operating Room).

As part of the project team, you will have the freedom to advise project leaders on the best way to solve problems and will be expected to deliver results as part of a team.

As an expert in your field, experienced in working to tight deadlines, you will manage project deliverables successfully and within deadlines. The role also includes client and contractor-facing activities where you will help ensure deliverables and transfer gained knowledge to the client.

You will leverage your experience in developing software within the relevant regulatory frameworks and processes and, most importantly, see your unique work and ideas launched into the market by some of the big medico players in the world.

Another part of the role is to support a service hub, implementation, and development of software required for production-oriented applications and afterwards support validation and implementation of those.

Responsibilities:

• Participation in R&D projects for new medical devices
• Preparation of technical and quality documentation related to software development
• Designing and conducting tests on prototypes
• Cooperation with technical consultants and suppliers

Requirements :

• Bachelor’s degree in Computer Science, Electrical Engineering, or related technical field
• Computer science, programming, telecommunication, Robotics, or similar IT, with practical experience in medical device software development preferred
• At least 3 years of experience in a similar position
• Extensive knowledge in software validation, quality, or engineering (not necessarily coding)
• Experience with laboratory equipment
• Experience in Unit/Integration level testing
• Understanding of FDA 21 CFR 820 and IEC 62304 software development standards is highly desired
• Knowledge in MISRA C (nice to have)
• Embedded C/C++ programming. Mid/High skill. Advantage if already on Microchip
• Basic knowledge of working with Octave, MatLab, or Python (to document scripts)
• Documentation skills, i.e., creating Architecture, Detailed Design
• Ability to use measuring equipment
• Self-motivated and accustomed to getting on with tasks with a thirst for new technologies and using the most appropriate software language
• Ability to work as part of a small team to an aggressive timescale and with strict attention to detail

We offer:

• Working in the R&D department in an international, interdisciplinary team
• Great atmosphere in the office and interesting challenges
• Opportunity to grow with the organization and build a successful career path
• A number of benefits (private medical care, sports card, flexible working time, English lessons)

Please add the following clause: I consent to the processing of my personal data for the purposes of the recruitment process (in accordance with the Act of May 10, 2018 on the protection of personal data and in accordance with the Regulation of the European Parliament and Council (EU) 2016/679 on the protection of natural persons with regard to the processing of personal data and on the free movement of such data, and repealing Directive 95/46 / EC (GDPR)).

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