Jobs at ARTIDIS AG

Contribute to end-to-end mechanical design, prototyping, and documentation for a medical device platform. Produce 3D models and technical drawings, perform design verification and prototype testing, ensure ISO GPS compliance and medical-device regulatory alignment, collaborate with mechatronics and suppliers, and support transition to manufacturing and prototype maintenance.

As an AI Engineer in NLP, you'll design and deploy NLP systems, bridging ML and backend architecture, ensuring the reliability and compliance of AI solutions.

The Quality Assurance Manager oversees quality processes and systems per regulatory standards, ensuring compliance through documentation, audits, and cross-departmental collaboration.

The Fullstack Software Engineer will design, develop, and maintain software solutions, working with cross-functional teams to align on project goals and improve software performance.

The Clinical Study Manager oversees planning and execution of clinical studies for medical devices, ensures compliance with regulations and manages study operations and documentation.

The AFM Scientist will conduct AFM research, develop measurement protocols, ensure data quality, provide training, and support clinical operations. Requires on-site work and travel in the USA.

The Clinical Research Associate supports and oversees clinical studies, ensuring compliance with protocols and regulations while collaborating with sites and managing data.

The Quality Assurance Manager documents and reviews quality processes to ensure compliance with EN ISO 13485, oversees the quality management system, collaborates across departments, and supports regulatory inspections and audits.

As an AI Engineer NLP, you will design and deploy NLP systems, bridging ML and backend platforms, ensuring performance and regulatory compliance.

Plan, execute, and document software verification, regression, and system testing for a medical device. Develop test strategies, automated script-based tests, and maintain traceability to requirements. Support regulatory compliance (including FDA), produce release/compliance documentation, and collaborate with software, mechatronics, validation, and production teams to resolve anomalies and improve test automation and processes.