Hybrid Regulatory Affairs Expert

About the Company ZEISS is technology and innovation. Founded in Germany, in 1846, ZEISS is an internationally leading technology enterprise operating in the optics and optoelectronics industries across 50 countries. As a company wholly owned by a foundation, ZEISS is committed to responsibility in all its activities. As a pioneer in scientific optics,...

Overview In this Regulatory Affairs Lead role, you shape IVD regulatory strategies, guiding performance evaluation and marketing authorizations. You will act as the regulatory lead for global project teams, coordinating interactions with authorities and ensuring compliant submissions. The role supports lifecycle management and continuous improvement within...

ZEISS in Castiglione Olona, Italy, seeks an Injection Product Expert to drive end-to-end development and industrialization of injection-molded Sun Lens products. You will coordinate across Engineering, Production, Quality, Regulatory Affairs, and Logistics to bring projects from feasibility to production readiness and market launch. You will manage molds,...

Overview In this role you will be the primary owner of the local financial control framework for ERM's Italian entities, ensuring financial integrity, statutory compliance, and a robust controls environment. You will collaborate with the GDC, external auditors, tax advisors, and regional teams to maintain Italian GAAP compliance and provide...

Overview In this Azure Architect role you design scalable, secure Azure architectures that enable business transformation. You work with cross-functional stakeholders to translate objectives into robust cloud solutions and guide migrations from on-premises to Azure. You will shape architecture across strategy and migration initiatives, driving long-term...

Overview In this role you will provide medical leadership for clinical trials, guiding scientific strategy, trial execution, and reporting. You will serve as the internal medical expert for study results interpretation and contribute to protocol and project design. You will collaborate with cross-functional teams to manage safety, regulatory documents, and...

Overview In this role you help clients and stakeholders tackle complex fraud, disputes and regulatory challenges within KPMG's Forensic Team in Milan. You will contribute to national and international investigations, bring expertise in fraud risk and corporate compliance, and support high-stakes advisory projects. You'll work closely with clients...

Overview In this role you lead medical, scientific, and strategic direction for clinical trials and act as the internal medical expert for study results. You will shape study design, protocols, and project plans while ensuring rigorous evaluation and reporting. You collaborate across departments and with sponsors to support proposal development and trial...

Overview In this role you will provide medical leadership for clinical trials and serve as the internal medical expert for study reports and regulatory documents. You will guide study design and project plans while ensuring safety and scientific integrity across trials. You'll collaborate with cross-functional teams and support business development...