Stellenbeschreibung
Support development, integration, and validation of medical devices and healthcare systems Utilize engineering tools and methodologies for testing, data analysis, and system verification Collaborate on software and/or system engineering activities, including requirements definition and documentation Ensure compliance with relevant medical regulations and standards (e.g., ISO 13485, IEC 62304) Contribute to system integration activities involving hardware, software, and medical devices Maintain documentation of development activities, test procedures, and results in line with quality standards Generate reports to communicate findings, support regulatory submissions, and drive continuous improvement
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