1 bästa jobbet som designer level i malmö, m (Rekryterar nu!)

Contribute to the design and development of new MedTech products as part of a cross-functional project team.
Define software requirements and specifications based on product standards, requirements, and risk analysis.
Plan, execute, document, and report software verification activities.
Test and evaluate embedded software to ensure functionality, performance, reliability, and compliance with applicable standards.
Integrate and verify software developed by other engineers.
Contribute to system-level risk analysis and product verification activities.
Ensure compliance with relevant medical device regulations and standards, including FDA, MDR, and ISO requirements.
Participate in technical design reviews and maintain required product and project documentation.
Provide technical support to Manufacturing, Quality Assurance, and Operations when needed.

Requirements

BSc or MSc in Electrical Engineering, Computer Science, Software Engineering, or a related field.
Experience with embedded software and testing in electromechanical systems.
Experience with real-time operating systems (RTOS).
Experience with test automation and scripting.
Hands-on experience with diagnostics and debugging of embedded software.
Understanding of software verification in regulated product environments.
Knowledge of medical device standards such as IEC 62304 and IEC 60601-1.
Familiarity with modern software testing strategies, tools, and practices.
Good understanding of product risk management.

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