Programming robotic systems for autonomous test execution of contrast media injectors. Developing flexible software frameworks for test sequence configuration. Quantifying efficiency gains versus manual testing.
ISO 9001 quality processes, supplier evaluations, CAPAs and complaints for mechanical devices, microfluidic chips or chemicals. Life-sciences or engineering degree/certificate and 1+ year of relevant experience required. Employee stock purchase plan.
Developing digital twin models for contrast media injectors in diagnostic imaging. Research and transform scientific knowledge into practical applications. Focus on virtual verification and reliability engineering.
Maintaining CE approval files and checking labels and marketing materials for consumer health products. EN ISO 13485/ISO 9001 knowledge and experience with CE, WEEE, REACH, RoHS and CLP compliance required. Flexible hours, work-from-home policy, and extra flexi-days after year one.
Prototyping low-latency camera-to-display pipelines with robotic telemetry overlays for precision medical robotics. Related master’s enrollment or final-year bachelor’s study, Python or C++, Linux, Git, and vision/ML fundamentals required. Autonomous prototyping on edge hardware.
European clinical studies, registries, and manuscripts for robotic-assisted surgery. Four years of people management required; 8–12 years in clinical affairs or research project management preferred. Coordination across global teams, hospitals, KOLs, and medical societies.
Developing manufacturing processes for surgical instruments and accessories. 5+ years in industrialization for complex medical devices required. Autonomy and flexibility in a cleanroom environment.
Leading a multidisciplinary engineering team in medical device product industrialization. 5 years of people leadership experience required. Short-term incentive plan and competitive compensation.
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Onsite and remote consulting for robotic-assisted surgery implementation and optimization. Detailed knowledge of medical device reprocessing regulations required. Collaboration with hospital stakeholders and internal departments.
Production test systems and series manufacturing for confined-space inspection drones. Electronic product certification experience required. KiCAD, board bring-up, and manual or reflow soldering in the production setup.
Developing high-precision mechatronic subsystems for surgical robots. 3+ years mechanical design experience with robotics platforms required. Structured onboarding, autonomy and flexibility.
Designing and prototyping robotic interfaces and custom hardware for an automated biology lab. Hands-on experience with CAD and 3D printing required. Workshop environment with hand and power tools.
Designing and troubleshooting EHS technical systems for medical device manufacturing. Federal STPS certification or equivalent required. Flexible benefits package, MIP bonus.
Ensuring compliance with EU MDR and Swiss MedDO for robotic-assisted surgery devices. 4+ years medical device industry experience required. Hybrid work, 5-person regulatory team.
Troubleshooting drone hardware and software issues for indoor inspection technology. 5+ years technical customer support experience required. Weekly gym sessions, modern offices with free snacks.
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