Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a
Company Description At Intuitive, we are united behind our mission: we believe that minimally invasive care is life-enhancing care. Through ingenuity and intelligent technology, we expand the potential of physicians to heal without constraints. As a
Overview In this role you will lead CDx regulatory strategy for pharmaceutical, biotech, and diagnostic programs. You will partner with cross-functional teams to align diagnostic development, biomarker strategy, and clinical trial plans with regulatory expectations and commercialization goals. You
Overview In this role you drive the design and execution of early-stage oncology clinical development plans, leading cross-functional teams to translate strategy into patient-ready programs. You will shape trials, contribute to regulatory and Medical Affairs strategies, and evaluate
Overview As Senior Clinical Program Lead, you will drive phase II–III development for obesity and liver diseases within a newly formed Global Clinical Development group. You will steer cross-functional teams to deliver high-quality trial execution and shape
Overview In this role you will lead CDx regulatory strategy for pharmaceutical, biotechnology, and diagnostic clients, translating global requirements into practical plans. You will shape regulatory pathways for companion diagnostics and clinical trial assays, aligning biomarker strategies with
Overview In this Program Manager role, you will oversee contractual, commercial, and relationship activities with suppliers, government bodies, and international organisations to develop European contracts and services in the semiconductor sector. You will engage with EU funding
Overview In this role, you drive early-phase obesity and liver programs from strategy through execution, leading cross-functional teams to advance therapies. You’ll influence regulatory strategy and contribute to Medical Affairs plans, shaping evidence generation and decision-making across development.
Overview In this role you will lead the design and delivery of multi-country benefits financing programs for multinational clients, with a focus on UK, Europe and Asia and up to 30% international travel. You’ll work within Global
Overview In this high-impact field role, you will serve as BeOne’s medical affairs representative to external medical communities, shaping scientific exchange and partnerships with HCPs and KOLs. You’ll translate complex data into actionable medical insights, support
Overview As Country Medical Director for Germany, you lead BeOne’s Medical Affairs strategy and governance, aligning local efforts with European and Global priorities. You act as the senior scientific voice for Germany, shaping medical strategy, evidence-generation
Overview In this role you will be a technical security leader responsible for designing and optimizing Deel’s core security platforms. You will own the lifecycle of multiple security solutions, improving defense-in-depth and ensuring regulatory compliance across a
Overview As an Advanced MES Consultant, you will drive MES strategies and implementations for leading life sciences companies across Europe. You’ll collaborate with cross‑functional teams to translate requirements into robust MES architectures and integrations, supporting global
Overview In this role you will shape identity strategy for high-value opportunities across EMEA, engaging executives to translate identity security into business outcomes. You’ll influence decision-makers early in the sales cycle, framing problems and aligning programmes
Overview In this role, you will lead clinical trial operations for sponsor-specific partnerships in Germany, overseeing site and central monitoring with a focus on patient safety and data integrity. You will collaborate with cross-functional teams to
Overview As Clinical Development Lead for CRM, you will own the strategic and operational direction of the clinical development plan for this asset in Germany. You will guide a team of clinical leaders to execute a
Overview As a Project Manager in Medical Writing, you lead and develop a capable team to deliver compliant, high-quality medical writing outputs within sponsor partnerships. You align with clinical development objectives and collaborate across functions to
Overview As Director, you will lead BeOne’s Healthcare Compliance program across Germany, the UK and Ireland, acting as a senior strategic partner to leadership. You will shape risk-based compliance strategy and governance to enable responsible business growth,
Overview As the regional trade compliance expert for EU/UK/CH, you manage import/export compliance, licensing, classifications, and sanctions, collaborating with brokers and authorities. You will monitor regulatory changes, develop controls, and support audits while ensuring seamless cross-border operations.
Overview In this role you will lead AI conformity efforts under evolving EU AI regulations, establishing BSI as a global authority in AI regulation and accreditation. You will shape processes, policies, and staff competence to ensure