Deadline: December 15, 2026 The Italian Institute of Artificial Intelligence (AI4I) is seeking for talented and ambitious Heads of R&D Laboratories to lead the next generation of AI research and development in AI-driven industries APPLICATION DEADLINE
WHO WE ARE: A leading partner to the world’s major cloud providers, including AWS, Azure, and Google. The formation of Accenture Cloud First, with a $3 billion investment over three years, demonstrates our commitment to deliver greater
WHO WE ARE: A leading partner to the world’s major cloud providers, including AWS, Azure, and Google. The formation of Accenture Cloud First, with a $3 billion investment over three years, demonstrates our commitment to deliver greater
CTP (Culture, Thinking & People) provides accredited Continuing Medical Education (CME) programs that serve as a benchmark for improving clinical practice, patient care, and quality of life. We design programs tailored to different healthcare professionals and
About Us JINGDONG Logistics (JD Logistics) is the logistics arm of JD.com and one of the worlds leading technology-driven supply chain solutions providers. Leveraging advanced expertise in automation, intelligent logistics, and data-driven operations, we deliver end-to-end
At Siemens Healthineers (SHS) Radiopharma, we are committed to driving sustainable progress through cutting-edge technology. We empower our customers by bridging the physical and digital worlds—enhancing the way we live, work, and move, today and for
This opportunity is located in Turin, Italy. The Italian Institute of Artificial Intelligence (AI4I) is seeking for talented and ambitious Heads of R&D Laboratories to lead the next generation of AI research and development in AI-driven
Discover a more connected career As the Supervisor Inventory Mgt (Materials Supervisor), you will be responsible for ensuring materials are always available at the location level to complete production. Indirectly working with Operations and Finance teams
We’re looking for a medically qualified professional to support Market Access Strategy, ensuring our portfolio is positioned for timely and appropriate patient access. This is a high-impact role at the intersection of clinical science, evidence generation
Overview In this role you will support worldwide post-approval regulatory activities focused on CMC for vaccines or biological products. You will work within a regulatory team to shape submission strategies, assess quality-related changes, and coordinate cross-functional