Luxembourg-Relocation Senior Regulatory Compliance Officer

Thermo Fisher Scientific in Italy is seeking a Senior Regulatory Affairs Specialist to lead global disclosure and regulatory submissions, ensuring compliance with ICH and regional requirements across product development from preclinical to registration. xlwpduy È essenziale assicurarsi di soddisfare i requisiti per questo ruolo; la preghiamo di leggere...

Overview In this senior regulatory role, you provide strategic legal guidance across the lifecycle of Illumina’s medical devices, diagnostics, and life-science products in EMEA and Latin America. You collaborate with cross-functional teams to enable compliant product development, submission, and post-market activities in a fast-paced, international...

Overview As a Senior Regulatory Affairs Associate, you will drive post-approval regulatory activities focused on CMC for biological and vaccine products. You will collaborate across manufacturing, QA, QC, and regulatory teams to shape submission strategies and ensure worldwide compliance. Your work supports variations, renewals, and market expansions,...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Sr Regulatory CMC Consultant - Small Molecule & Veeva RIM Must Have based in Italy.Se i requisiti e l'esperienza richiesti per questo lavoro corrispondono alle sue competenze, la preghiamo di candidarsi tempestivamente.We are...

Overview As Senior Global Patient Safety Physician at Chiesi, you lead safety science for assigned products, shaping proactive risk management and safety surveillance. You collaborate across Clinical Development, Medical Affairs, Regulatory, Quality and external partners to integrate safety data into development plans and submissions. You drive science-led...

Overview In this role, you will lead the industrialization, validation and lifecycle management of Device Constituent Parts and device platforms, ensuring scalable, compliant development and technology transfer. You will drive cross-functional alignment across R&D, Quality, Regulatory, Manufacturing, and external partners to secure regulatory compliance and...

Overview Senior Site Contracts Lead to guide site contract lifecycle across studies, ensuring compliant negotiations and templates. You will coordinate with country experts, sponsors, and the Contracts Department to manage NDAs, CTAs, amendments, and related documents. The role focuses on risk mitigation, timeline control, and regulatory alignment to enable...

Overview In this role you steer the global clinical development strategy for key respiratory indications, leading a physician-scientist team across geographies. You will align R&D and commercial goals, shape trial designs, and drive regulatory success with high scientific and operational impact. You thrive in a cross-functional, matrix environment and help...

Overview In this role you will provide strategic legal support for European R&D activities and select markets, partnering with regional and global teams to navigate clinical trials, regulatory, data privacy, and vendor relations. You will translate complex regulations into practical risk mitigations while supporting global programs across diverse...