Work Flexibility: Hybrid or Onsite Who we want: We are looking for a passionate and inspiring leader for the intramedullary nailing (IMN) platform with profound knowledge about design development as well as the Trauma and especially
At Elanco (NYSE: ELAN) – it all starts with animals!As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
At Elanco (NYSE: ELAN) – it all starts with animals!As a global leader in animal health, we are dedicated to innovation and delivering products and services to prevent and treat disease in farm animals and pets.
Overview In this role you drive regulatory strategy and submissions for multi-region studies, coordinating CTAs, regulatory applications, and trial milestones. You will lead cross-functional teams to ensure compliant, timely submissions and smooth study startup across EU and global
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.
Overview In this role you will shape global CMC regulatory strategies for veterinary biologics, supporting geo-expansion and post-approval changes. You collaborate across R&D, Manufacturing, Quality and regulatory partners to enable registrations and timely submissions. You will lead pre-submission
Overview In this role you will shape global regulatory CMC strategy for veterinary biocides, pesticides and topical products, author submissions, and oversee lifecycle management from development through approval and renewals. You’ll collaborate with R&D, Manufacturing and Quality,
About the RoleLeads and evaluates medac’s Managed Access Programs (MAP) and Named Patient Use (NPU) requests from a clinical and ethical perspective, ensuring robust benefit–risk assessments and patient-focused decision-making.Hands-on Medical Expert responsible for executing clinical-scientific activities
Overview Join Vishay as a Senior Workday HRIS Analyst / Team Lead to drive global Workday solutions. You will lead rollout and optimization of Core HCM and advanced modules, shaping compensation, job architecture, and reporting across
Overview As Technical Asset Manager, you will oversee the operational phase of renewable energy assets, ensuring technical performance, compliance, and optimisation across a growing portfolio. You will bridge internal teams and external partners to drive asset
Overview In this role you will provide legal leadership on AI governance, privacy, and data protection across global operations. You will partner with AI/Data teams to implement controls and document Responsible AI practices. You will oversee
Overview In this role you ensure scientifically sound, compliant clinical documentation to support development, approval, and commercialization of medical devices. You partner with cross-functional teams to address scientific and regulatory questions, improving product documentation, regulatory submissions, and post-market activities. You
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 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
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 and evaluate managed access and named patient use requests from a clinical and ethical perspective, ensuring sound benefit–risk rationale. You will produce high-quality regulatory documentation and support global submissions across the
Overview In this Principal Consultant role, you guide Regulatory Affairs strategy and growth within NNIT’s Life Sciences practice. You’ll lead client engagements, drive RFP responses, and shape business development initiatives to expand the Regulatory Affairs portfolio. The position
Overview As Technical Specialist & Scheme Manager, you will support the certification of active medical devices for the European market. You will review technical and clinical documentation, manage certification activities, and provide regulatory guidance across CE marking schemes.
Overview As Senior Accountant, you will manage day-to-day accounting, support year-end audits, and ensure accurate financial reporting for RP Globals renewable energy portfolio. You will work with internal stakeholders, external auditors, tax advisors, and payroll providers
Overview In this role you support the JPMSE Recovery & Resolution agenda and act as the primary contact for senior management and regulators. You collaborate with Finance, Risk, Business Management, Treasury and Operations to coordinate plans,