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 input for
POSITION SUMMARY We are looking for a C++ Developer (freelance/P.IVA) to consolidate LivGemini’s existing medical imaging, computational and analytical components into a unified C++ software platform. The selected contractor will be responsible developing a new application
Role : Administrative Manager (Remote) Location : Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking an Office and Administrative Domains specialist to work on a Full-Time basis. The role
Independent Investment Advisor Balfour Capital Group This is an independent contractor engagement. Compensation is structured on a commission-only, production-linked basis; no base salary or guaranteed income is associated with this role. Candidates should have established client
As an energy park developer, the UKA Group plans, builds, operates, and sells wind, photovoltaic (PV) and battery storage projects. It contributes to a sustainable power supply in Germany, Europe and America that is independent of
About the Role: We are seeking a dynamic and technically skilled Technical Solutions Manager to join our team specializing in Battery Energy Storage Systems (BESS). This role is pivotal in designing and delivering tailored technical solutions
Role : Compliance Attorney (Remote) Location : Remote (Work from Anywhere) Role Overview: We are hiring for one of our clients, seeking a Compliance Attorney to work on a Full-time basis. The role involves providing legal
Overview In this role you lead AI validation and governance across traditional ML and GenAI/agentic AI, shaping the group’s model risk framework. You provide independent oversight through the full AI lifecycle and stay hands-on with design,
Overview In this role, you will help maintain and improve the Quality Management System to meet customer and regulatory requirements. You’ll act as the main quality liaison for Italian-market customers, driving issue resolution and process improvements. You
Overview In this role you join our Medical Device Notified Body as an Internal Clinician, bringing clinical expertise to support conformity assessments. You will review technical documentation and clinical evidence to judge sufficiency and quality of data.