Make your mark for patients We are looking for an Environmental Regulatory Intelligence Lead who is strategic, analytical, and collaborative to join our Environmental Sustainability team, based at our UCB HQ located in Brussels, Belgium. About the
Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It
Regulatory Liaison ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster. As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the
Regulatory Affairs & Pharmacovigilance Specialist At Fresenius Medical Care, we are the global leader in kidney care, committed to improving the lives of patients with chronic kidney disease. Our mission is to deliver high-quality, innovative products, services,
The Clinical Research Regulatory Coordinator is responsible (primarily or in supporting role) for all activities related to the submissions of clinical trials applications in the CTR online platform known as Clinical Trial Information System (CTIS). The submitted
Regulatory Engineer (Pre-Commissioning) As a Regulatory Engineer, you will support the Pre-Commissioning phase of a major industrial project. You will review technical and regulatory documentation and ensure that all required documentation is complete and compliant before Commissioning. Both experienced engineers and
Assay Development Scientist - Genomics Services (Hybrid) Are you a scientist with expertise in molecular genetics and genomics technologies? Join CellCartas Genomics Services team as an Assay Development Scientist and contribute to the advancement of innovative
Who we are At Platform Science, we’re working to connect everything that moves. Founded in 2015, we are an open IoT platform that partners with innovative fleets, application developers, vehicle manufacturers, and equipment providers in the
Summary of Responsibilities: Site management responsibility for clinical studies according to Fortrea’s Standard Operating Procedures, ICH GCP Guidelines, applicable project plans and Sponsor requirements, including verification of study training records. Conducts site monitoring responsibilities for clinical
Make your mark for patients We are looking for a GMP Process and Operations Compliance Lead who is collaborative, quality‑driven, and proactive to join our Clinical Manufacturing team (Pharma and Biologicals, mAb and Gene Therapy), based
Work ScheduleStandard (Mon-Fri) Environmental ConditionsOffice Job Description SUMMARY The Senior Application Administrator is responsible for the administration, configuration, validation, and lifecycle management of laboratory middleware and instrument interfaces within a regulated GxP environment. This role serves
Make your mark for patients We are looking for a Senior Real World Evidence Expert who is scientifically rigorous, strategically minded, and collaborative to join our Real‑World Evidence (RWE) team, helping to shape evidence generation strategies
Be part of a movement to change the way Europe pays In today’s digital Europe, payments still feel too complicated. Random delays, confusing rules, extra apps and accounts make it harder than it should be to
Clinical Study Specialist I Are you a clinical operations professional who thrives on precision, compliance, and process efficiency? We are looking for an energetic Clinical Study Specialist I to join our growing Clinical Operations team and
At EY, we’re all in to shape your future with confidence. We’ll help you succeed in a globally connected powerhouse of diverse teams and take your career wherever you want it to go. Join EY and
At Capgemini Engineering, the world leader in engineering services, we bring together a global team of engineers, scientists, and architects to help the world’s mostinnovative companies unleash their potential. From autonomous cars to life-saving robots, our
Join Amazons Global Sustainable Packaging (GSP) organization as we pioneer the future of sustainable e-commerce packaging. As an Advanced Packaging Materials Engineer based in the EU, youll serve as the critical link between our European and
Let’s shape the future of finance - together At Isabel, we believe that real innovation happens when people and ideas connect That’s why we’re building more than technology, we’re building an ecosystem. One where every voice
Mission Overview: Keystone Solutions is seeking a Senior Business Analyst / Consultant for a consultancy mission at a client site in the Belgian healthcare sector. The consultant will be responsible for the functional analysis, feasibility study,
General information Publication date 23/08/2026 Position description Category OPERATIONS - CONSULTING Job title Drug Product Development and CMC Leader - Life Sciences - M/F/X Contract Permanent contract Job description About the Role As Drug Product Development