System (Safety) Engineer
Firmenname für PREMIUM-Mitglieder sichtbar
- Mai 2024
- Dezember 2024
- CH-Burgdorf
- auf Anfrage
- 12.04.2024
- CF-34276948_1712934426
Projekt Insights
Projektbeschreibung
Your main tasks:
* Define requirements and use cases for new and existing products and systems in collaboration with product management, business development and other stakeholders
* Define system architecture and interfaces to external systems
* Close collaboration with experts from development (hardware, software and mechanics), risk management, product management, human factors, production and other involved departments
* Close collaboration with verification teams
* Ensure coverage of standards and regulatory requirements
* Maintain the requirements, traceability and architecture in the requirements management tool over the product lifecycle (development through product care)
Your profile:
* Engineering degree (university or university of applied sciences) in electronics, software development, computer science or biomedical engineering
* Practical experience in interdisciplinary projects in a similar position
* Experience in the field of requirements engineering (IREB certification is an advantage)
* Experience in medical technology or other regulated industries
* Very good communication skills
* Very good English skills, good German is a plus
* Experience in the development of mechatronic medical devices
* Familiar with medical standards IEC60601, IEC62304
* Familiar with RiM standards ISO14971 and optional with AAMI TIR38
* Familiar with Functional Safety for Medical Devices (embedded systems)
* Experience in HW, ESW Development
* SysML, UML
Other Information
* Planned duration: 6 months +
* Extension: possible
* Workplace: Burgdorf
* Workload: 100%
* Remote/Home Office: 2 times a week onsite.
* Define requirements and use cases for new and existing products and systems in collaboration with product management, business development and other stakeholders
* Define system architecture and interfaces to external systems
* Close collaboration with experts from development (hardware, software and mechanics), risk management, product management, human factors, production and other involved departments
* Close collaboration with verification teams
* Ensure coverage of standards and regulatory requirements
* Maintain the requirements, traceability and architecture in the requirements management tool over the product lifecycle (development through product care)
Your profile:
* Engineering degree (university or university of applied sciences) in electronics, software development, computer science or biomedical engineering
* Practical experience in interdisciplinary projects in a similar position
* Experience in the field of requirements engineering (IREB certification is an advantage)
* Experience in medical technology or other regulated industries
* Very good communication skills
* Very good English skills, good German is a plus
* Experience in the development of mechatronic medical devices
* Familiar with medical standards IEC60601, IEC62304
* Familiar with RiM standards ISO14971 and optional with AAMI TIR38
* Familiar with Functional Safety for Medical Devices (embedded systems)
* Experience in HW, ESW Development
* SysML, UML
Other Information
* Planned duration: 6 months +
* Extension: possible
* Workplace: Burgdorf
* Workload: 100%
* Remote/Home Office: 2 times a week onsite.
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