238 English-speaking jobs in Schleswig-Holstein

Leads the development and execution of data products for R&D, translating business needs into product capabilities and managing the full product lifecycle. Partners with stakeholders to define product strategy, roadmaps, and technical solutions, ensuring regulatory compliance and user adoption.

PhD student position investigating carbon and GHG exchange in coastal environments impacted by marine Carbon Dioxide Removal (mCDR). The successful applicant will conduct field sampling, laboratory analysis, and collaborate with modelers and social scientists.

Lead Consultant for payment transaction strategy and innovation. Develop market-ready concepts, write industry content, and build a network of experts.

Software quality assurance engineer for Apple's Creative Music Apps team in Rellingen, Germany. Evaluate macOS, iOS & iPadOS products, create test plans, and ensure high quality and performance.

The Regional Medical Science Liaison serves as the primary point of contact for healthcare providers on clinical and scientific issues. The role involves delivering medical education, facilitating research, and gathering scientific insights. The MSL will provide scientific and medical data on products and indications, act as a medical expert at meetings, and facilitate communication between the client and investigators.

Software Engineers (m/f/d) join small teams to design, develop, test, deploy, and maintain software. Training is provided on project technologies. Experience in C/C++, Python, or Java is required.

Leads a series of global projects and programs with a total value of up to $10M, ensuring project accountability from initiation through closure. Manages project/program budgets, forecasts, tasks, schedules, risks, change management, and status reporting. Builds and nurtures relationships with business and IT leaders to support planning and project prioritization. Drives effective risk and issue management, ensuring processes are in place and effectively used. Ensures project team adheres to all standards, including ADF, quality, and compliance, as well as processes, defined technical capabilities, and guidelines.

Leads the end-to-end solution architecture for custom applications and complex integrations across HCM, Payroll, and Time & Absence. Partners with HR and HR IT stakeholders to ensure system alignment. Builds scalable, secure, and intelligent extensibility solutions using Workday AI and Enterprise GenAI.

The Specialist, Global Clinical Solution, eCOA delivers centralized services for drug projects, ensuring high-quality data from clinical operations. They manage eCOA and DPS projects, provide system and process training, and contribute to continuous improvement initiatives.

The Manager, Biosample Operations will lead coordination and tracking of human biological samples from clinical trials. Responsibilities include logistics, sample integrity, collaboration with clinical operations and laboratories, and managing sample analysis by external contractors.

Supply Chain Warehouse Specialist will manage GMP materials control and warehousing operations. Responsibilities include conducting reviews of GMP documentation, providing process improvement recommendations, and participating in receiving, shipping, inventory control, and distribution activities.

Leads the internal science engagement and communications strategy for Early Oncology and Precision Medicine. Develops and implements communication plans, drafts internal posts, and supports the SVP of Early Oncology & Precision Medicine with external and internal scientific presentations.

The Publications Delivery Lead (Senior Manager) will establish and lead a team responsible for end-to-end delivery of scientific publications. This role involves team leadership, operations management, and ensuring quality and performance excellence. The ideal candidate has experience building teams, implementing SOPs, and managing vendors.

Director will lead the development and maintenance of a global oncology real world data platform to support evidence generation. Responsibilities include managing data partners, developing standard operating procedures, and collaborating with cross-functional stakeholders. Requires 5+ years of experience in the pharmaceutical industry with oncology real world data and a BS degree in a science related field.

The Associate Director, Global Clinical Solutions Delivery serves as the primary point of contact for Global Study Teams, ensuring seamless connection for clinical technologies. Responsible for the setup, implementation, and maintenance of technologies, the role requires expertise in project management, E2E study management processes, and vendor collaboration.

Leads and innovates clinical operations for Vaccines & Immune Therapies, managing a team of Program Management Senior Directors. Provides strategic guidance for clinical trials, ensuring on-time, on-budget, high-quality delivery. Drives clarity and consistency across strategic processes, leveraging data insights and AI for optimization.

The Associate Director Regulatory Affairs - COE Submission Delivery Team Lead leads cross-functional submission teams for Marketing Authorisation Application (MAA) and Clinical Line Extension (CLE) submissions. This role requires strong project management abilities, regulatory submission experience, and the ability to identify and mitigate regulatory risks. The successful candidate will coach and mentor team members, partner with stakeholders, and drive transformational change in regulatory submissions.

This Postdoctoral Fellow position focuses on researching and developing next-generation 3D ex vivo culture systems to study the mechanisms of action for immuno-oncology drugs. The role involves designing and implementing innovative 3D models to study immune-modulatory compounds and their impact on peripheral immune responses against tumors.

Drive Lynparza and Imfinzi business growth by developing and executing marketing plans. Collaborate with cross-functional teams to maximize brand opportunities and manage the Lynparza life cycle.

Senior Medical Science Liaison providing scientific expertise in Neurology/Meta+ to healthcare professionals and key opinion leaders. Executes Medical Affairs Plans, fosters scientific partnerships, and bridges the gap between local and national product strategies. Requires 3-5 years of MSL experience, rare disease experience preferred.