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
Deine Aufgaben Als QS Manager:in verantwortest du die regulatorische Konformität rund um Verpackung und die Umsetzung der Verordnung (EU) 2025/40 “Packaging & Packaging Waste Regulation” (PPWR) und stellst gleichzeitig sicher, dass unsere Produktstammdaten abteilungsübergreifend vollständig, korrekt
Position Summary: The Director, CDx Regulatory Consultant will be responsible for applying deep expertise in companion diagnostic regulatory strategy, IVD development, quality system expectations, and global marketing authorization pathways to advise pharmaceutical, biotechnology, and diagnostic clients on the
Study Start Up Associate 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
Position Summary: The Director, CDx Regulatory Consultant will be responsible for applying deep expertise in companion diagnostic regulatory strategy, IVD development, quality system expectations, and global marketing authorization pathways to advise pharmaceutical, biotechnology, and diagnostic clients on the
The Local Study Associate Director (Sponsor dedicated) (m/w/d) will be leading Local Study Teams at country level to deliver committed components of clinical studies according to agreed resources, budget and timelines complying with Sponsor Procedural Documents, international guidelines such
YOUR CONTRIBUTION As a Regional Regulatory Affairs Manager (m/f/d), you will provide regional regulatory support for the strategic development, approval, and life cycle management of drugs, ensuring compliance with regulatory and legal requirements in the region APACMEA. This will
YOUR CONTRIBUTION As a Regional Regulatory Affairs Manager (m/f/d), you will provide regional regulatory support for the strategic development, approval, and life cycle management of drugs, ensuring compliance with regulatory and legal requirements in the region EU/UK/CH. This will
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals. When considering candidates, we look for scientific and business professionals who are highly motivated, collaborative, and most importantly, share our
Solaris is Europes leading embedded finance platform. Solaris’ full German banking license and proprietary modular B2B tech stack empowers its partners – from SMEs to large, multinational, non-financial companies – to offer compliant, customer-centric banking services,
Solaris is Europes leading embedded finance platform. Solaris’ full German banking license and proprietary modular B2B tech stack empowers its partners – from SMEs to large, multinational, non-financial companies – to offer compliant, customer-centric banking services,
Job ID 516070 Posted since 10-Aug-2026 Organization Siemens Healthineers Field of work Cybersecurity Company Siemens Healthineers AG Experience level Experienced Professional Job type Full-time/Part-time Work mode Hybrid (Remote/Office) Employment type Fixed Term Location(s) Erlangen - -
Our International Graduate Trainee Programme offers you exciting insights and a thorough introduction to the diverse activities of a leading global reinsurer. This provides you with the exceptional opportunity to advance your expertise and drive your
Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.
The Position Join us in advancing cutting-edge radiolabelled compound analytics. In your new role as a Postdoc, you will focus on analytical method comparison for the characterization of labelled compounds and the assessment of radiochemical stability.
Description Projects Managers with experience in Dermatology and/or Rheumatology are crucial to the success of Clinical Trials managed by Indero. They are the main point of contact internally as well as externally, ensuring all activities and
Clinical Research Associate, CRA II, Senior CRA 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,
The Senior Medical Affairs Manager – Lung Cancer (m/f/d) is responsible for supporting the development and execution of the Medical Affairs strategy for GSKs Lung Cancer portfolio in Germany. The role will focus on the preparation
Tätigkeitsbereich:Organisation und Recht Fachabteilung:Legal AI: AI Regulations, Ethics & Digital Regulations Gesellschaft:Mercedes-Benz Group AG Standort:Mercedes-Benz Group AG Zentrale, Stuttgart Startdatum:27.08.2026 Veröffentlichungsdatum:16.07.2026 Stellennummer:MER00045TJ Arbeitszeit:Vollzeit Bewerben Aufgaben The “Legal AI: AI Regulations, Ethics & Digital Regulations” team in