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Staff Software Engineer R&D
- Permanent
- Switzerland
- Information Technology
This vacancy has now expired. Please see similar roles below...
Proclinical is seeking a motivated and talented Staff Software Engineer R&D to join our client's team in Switzerland. In this role, you will be responsible for software development for life-sustaining medical devices. You will design and implement embedded software and desktop applications, and be involved in all aspects of the software life cycle in a highly regulated environment. You will use tools like Jira, Confluence, Git, and Jenkins, and write software in C/C++ and C#.
Please note that to be considered for this role you must have the right to work in this location.
Responsibilities:
- Design, develop, test, document, release, and maintain software for medical devices
- Organize work according to project priorities, deadlines, and deliverables
- Collaborate on interdisciplinary product development activities during the full life-cycle of class 2 and class 3 medical devices
- Lead new product development activities including verification and validation, such as test method development
- Support production activities for the introduction of new products
- Support regulatory submissions through required documentation
- Manage (sub-) projects on new product development and sustaining projects
Key Skills and Requirements:
- Degree in Computer Science, Software Engineering, or equivalent
- Experience in a similar position in the MedTech industry or another industry requiring functional safety certifications
- Proficiency in C/C++ and C#
- Experience in the complete software life cycle
- Understanding of software architecture principles and design patterns
- Strong collaboration and team-playing skills
- Excellent analytical and creative problem-solving skills
- Ability to produce quality documentation in English, meeting MedTech industry standards
- Fluency in German and English
Preferred Qualifications:
- Experience in Requirements Engineering, including product architecture and design transfer of requirements
- Experience in Design Verification & Validation planning and execution
- Experience in developing MedTech software according to IEC 62304
- Experience in Risk Management and Cybersecurity
If you are having difficulty in applying or if you have any questions, please contact Christian Andersen at c.andersen@proclinical.com
Apply Now:
If you are interested in learning more or applying to this exciting opportunity, please complete the form below and attach a copy of your CV. Alternatively, for further details or to talk directly to a life sciences recruitment specialist, please request a call back at the top of this page.
Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.
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