590 English-speaking jobs in Liguria

Senior Software Engineer to own end-to-end metrics collection from agent to backend. Design features and solve performance/scalability issues using Rust, Go, or C/C++. Requires systems programming background.

Senior Software Engineer to own end-to-end metrics collection from agent to backend. Design features and solve performance/scalability issues using Rust, Go, or C/C++. Requires systems programming background.

Design and deliver hands-on training demonstrating Sysdig across containers, Kubernetes, Linux, and cloud. Own the training platform's reliability and automate lab provisioning. Author courseware using AI tools.

Design and deliver hands-on training demonstrating Sysdig across containers, Kubernetes, Linux, and cloud. Own the training platform's reliability and automate lab provisioning. Author courseware using AI tools.

Design and deliver hands-on training demonstrating Sysdig across containers, Kubernetes, Linux, and cloud. Own the training platform's reliability and automate lab provisioning. Author courseware using AI tools.

The Senior Global Patient Safety Physician leads safety science for assigned products, shaping proactive risk management and surveillance. This role integrates safety data across development and lifecycle management through cross-functional collaboration.

Senior Clinical Project Manager coordinates operational management of clinical projects to advance the pipeline. This role liaises with CROs and stakeholders, ensuring study quality, timelines, and budget adherence while managing 1–3 clinical trials.

Lead industrialization, validation, and lifecycle management for Device Constituent Parts and platforms. Drive cross-functional alignment across R&D, Quality, and Manufacturing to ensure regulatory compliance and product robustness.

Lead governance for Air/Care and Rare product lifecycle management, partnering with R&D, regulatory, and manufacturing teams. This strategic role ensures global regulatory compliance and drives continuous improvement across quality systems.

Develop and validate analytical methods for protein-based products. This role involves method development, optimization, and troubleshooting to ensure robust product characterization. Requires 8 years of relevant lab experience or 5 years with a PhD.

The Senior Global Patient Safety Physician leads safety science for assigned products, shaping proactive risk management and surveillance. This role integrates safety data across development and lifecycle management through cross-functional collaboration.

Senior Clinical Project Manager coordinates operational management of clinical projects to advance the pipeline. This role liaises with CROs and stakeholders, ensuring study quality, timelines, and budget adherence while managing 1–3 clinical trials.

Lead industrialization, validation, and lifecycle management for Device Constituent Parts and platforms. Drive cross-functional alignment across R&D, Quality, and Manufacturing to ensure regulatory compliance and product robustness.

Lead governance for Air/Care and Rare product lifecycle management, partnering with R&D, regulatory, and manufacturing teams. This strategic role ensures global regulatory compliance and drives continuous improvement across quality systems.

Develop and validate analytical methods for protein-based products. This role involves method development, optimization, and troubleshooting to ensure robust product characterization. Requires 8 years of relevant lab experience or 5 years with a PhD.

The Senior Global Patient Safety Physician leads safety science for assigned products, shaping proactive risk management and surveillance. This role integrates safety data across development and lifecycle management through cross-functional collaboration.

Senior Clinical Project Manager coordinates operational management of clinical projects to advance the pipeline. This role liaises with CROs and stakeholders, ensuring study quality, timelines, and budget adherence while managing 1–3 clinical trials.

Lead industrialization, validation, and lifecycle management for Device Constituent Parts and platforms. Drive cross-functional alignment across R&D, Quality, and Manufacturing to ensure regulatory compliance and product robustness.

Lead governance for Air/Care and Rare product lifecycle management, partnering with R&D, regulatory, and manufacturing teams. This strategic role ensures global regulatory compliance and drives continuous improvement across quality systems.

Develop and validate analytical methods for protein-based products. This role involves method development, optimization, and troubleshooting to ensure robust product characterization. Requires 8 years of relevant lab experience or 5 years with a PhD.