238 germany English-speaking jobs in Schleswig-Holstein

HVAC Design Engineer needed for Basic Design of HVAC systems in shipbuilding projects using Cadmatic. Experience in interpreting P IDs, writing technical specifications, and collaborating with subcontractors is required. Fluency in English is essential, German is a plus.

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.

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.

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.

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.

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 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.

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.

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 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.

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.

The Medical Director, Patient Safety Physician is responsible for the Clinical Safety strategy for assigned AstraZeneca drug projects and products throughout development and/or marketing. This role involves safety assessment, risk management, and communication of safety topics across regulatory documents. The Medical Director collaborates with experts across AstraZeneca and provides medical input to ensure risk-minimization strategies are implemented appropriately.

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.

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.

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.

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.

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.

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.