Biomedical engineer or engineer for the management of operating units - 100% — HUG
NewCHF 49'500 - 75'000
HUG · Genève (GE)
- Location
- Genève
- Contract
- full-time
- Posted
- Yesterday
SalaryCHF 49'500 - 75'000
Role overview
As part of the creation of the Operating Blocks Directorate (DBO), you will play a central role in the strategic and operational management of biomedical equipment.
You will contribute to the multi-year planning of medical devices necessary for surgical activities, ensure the updating of the inventory and participate in the management of capital assets for transverse and specialty-specific equipment.
As a referent or technical reference, you bring your expertise to mini-COMs, accompany users in expressing their needs, evaluate existing solutions and challenge requests in relation to institutional orientations.
- As part of the creation of the Operating Blocks Directorate (DBO), you will play a central role in the strategic and operational management of biomedical equipment.
- You will contribute to the multi-year planning of medical devices necessary for surgical activities, ensure the updating of the inventory and participate in the management of capital assets for transverse and specialty-specific equipment.
Application process
- You are involved in the management of medical devices (DM and DMI), loan applications, related contracts, and the monitoring of cross-cutting projects such as Optimat.
- You are involved in the renovation and development projects of the operating units as consulting engineer or consulting engineer to the architects and agents project leaders.
- You define equipment requirements, develop technical programs, specify the constraints of implementation and accompany team coordination and training.
- Your role is crucial to ensure consistency between infrastructure, technology and clinical practices.
- In a context of rapid innovation, you ensure an active technological watch in connection with surgical and biomedical teams.
- You evaluate the new solutions, participate in specialized training and congresses and provide informed guidance to the competent authority.
- You contribute to managing the risks associated with medical devices, ensuring their regulatory compliance and working closely with the materials commission.
- You are involved in quality assurance and continuous improvement within the BOD.
