205 germany English-speaking jobs in Schleswig-Holstein

Painter (Lackierer) / Industrielackierer / Spritzlackierer Luftfahrt (m/w/d) needed for Wheels and Brake Shop in Norderstedt. Responsibilities include inspection, preparation, and painting of wheels and brakes according to documentation. Requires completed training as an aircraft/vehicle painter or comparable, relevant experience, and understanding of technical drawings.

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.

Manages and guides the development and approval of complex medical device labeling content, ensuring compliance with regulations and policies. Leads product use information initiatives across departments, managing projects from initiation to completion. Utilizes labeling software and tools to support the process.

Internship with Stryker's R&D Simulation team focused on advanced bone morphology analysis tools for orthopedic medical devices.

The Global Study Associate Director leads cross-functional study teams, ensuring successful study delivery according to timelines, budget, and quality standards. Accountabilities include leading study team communication, developing study documents, overseeing external service providers, and managing study budgets. The GSAD ensures compliance with regulations, policies, and best practices.

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.

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.

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.

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 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.

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.

Enterprise Process Expert will support the development and delivery of Direct Purchasing processes within the Procurement, Materials Management & Accounts Payable Team. This role will leverage SAP S/4HANA capabilities to realize defined processes and ensure alignment with the strategic direction of the Enterprise Process Owner.

The PATHS Strategic Partner shapes and drives the generation and integration of rare disease patient insights to inform disease strategy from drug development through commercialization. This role connects perspectives across HCPs, payers, regulators, and patients to drive rare disease patient access to medicines.

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.

Leads global patient advocacy strategy and engagement for Alexion Rare Disease Business unit. Responsible for building and enhancing strategic alliances with patient advocacy organizations to drive patient-centric goals. Collaborates with cross-functional teams to advance patient-focused drug development and ensure patient perspectives are integrated into decision-making. Requires 10+ years of industry experience or 7+ years in patient advocacy, including global/international roles.

The Associate Director, Quality Management provides guidance on quality standards and compliance for Late Development Oncology Clinical Operations. The role involves reviewing and improving the Quality Management System, supporting the execution of the Late Development Oncology Clinical Operations Quality Framework, and providing quality and compliance advice to clinical operations staff.

Leads and coordinates cross-functional study teams to ensure clinical study progress according to timelines, budget, and quality standards. Provides operational oversight for clinical studies, collaborates with internal and external stakeholders, and ensures compliance with regulations.

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.