238 germany English-speaking jobs in Schleswig-Holstein

Internship in 3D bone analysis and simulation for the development of orthopedic medical devices. You will work with a cross-site database of bone data and 3D models, perform statistical analysis, and contribute to product development.

Provides technical expertise and solutions to support sales. Analyzes customer specifications, recommends product configurations, and guides implementation planning. Develops technical presentations and collaborates with internal teams.

The Institute of Material Systems Modeling at Helmholtz-Zentrum Hereon is offering a 3-year PhD position in computational materials science and phase-field modeling. The project focuses on developing a novel phase-field approach for modeling the solid-state sintering of magnesium alloy powders.

The Institute for Cardiogenetics at the University Medical Center Schleswig-Holstein seeks a Postdoctoral Researcher in Data Science/Bioinformatics/Computational Biology. The successful candidate will apply bioinformatic methods to WGS and scRNA Seq data, perform statistical analysis, and contribute to research publications and grant applications.

Mechanical & Piping (M&P) Inspector required for LNG terminal project. Responsibilities include technical oversight, contractor management, static equipment & piping oversight, construction monitoring, pre-commissioning & commissioning support, and reporting. Requires a degree in Mechanical Engineering, minimum 10 years of experience in the Oil & Gas sector, and knowledge of ASME B31.3, API standards, PED 2014/68/EU, and relevant EU/German regulations. Fluent English required.

Sales Specialist for open source data platform in the UK. 5-7 years B2B enterprise software sales experience in data and analytics required. Understanding of open source software business models and modern data technologies.

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.

Internship at a leading medical technology company focused on 3D bone analysis and simulation. Contribute to the StrykerOrthopaedicModeling and Analytics (SOMA) database, perform statistical analysis, and communicate findings to colleagues.

Leads the development and execution of the franchise strategy for rare disease products, driving growth, profitability, and patient impact. Manages P&L, leads cross-functional teams, and ensures compliance.

Designs, implements, and evaluates marketing activities for assigned brand, including distribution channel solutions. Analyzes market data and identifies growth opportunities. Collaborates with internal and external teams to execute marketing plans.

Develop and optimize manufacturing processes for lentiviral vectors. Execute experiments, design bioreactor studies, and support cell line development. Collaborate with cross-functional teams to ensure manufacturability and contribute to technology transfer.

Manages the preparation and delivery of CMC documentation for regulatory submissions, ensuring compliance with AstraZeneca systems and procedures. Develops and applies expertise in regional regulatory requirements and contributes to business process optimization.

Automation Engineer provides technical support, resolves automation issues, and manages the lifecycle of assigned systems. Analyzes information to develop solutions and participates in continuous improvement activities.

Provides administrative support including calendar management, meeting/event coordination, departmental activities, documentation maintenance, and budget/expense tracking.

The Senior Manager, Digital Customer Strategy leads the development and execution of digital engagement strategies across assigned oncology portfolios. This role designs omnichannel campaigns, integrates AI solutions, and partners with cross-functional teams to optimize customer interactions and maximize business impact.

Leads a complex, science-led portfolio, prioritizing investments, aligning resources, and ensuring disciplined delivery to improve speed, quality, and cost. Collaborates with executive leaders, business units, and project sponsors for decision-making and portfolio steering. Manages portfolio performance reviews, analyses, and reporting. Drives adoption of portfolio management best practices, tools, and governance processes. Executes financial and resource management tasks across the portfolio, including forecasting, scenario modeling, and tracking. Provides financial models and visualizations of costs, demand/supply, productivity, and benefits realization. Communicates effectively with stakeholders and drives alignment across functions.

The Clinical Research Associate (CRA) is responsible for the delivery of clinical studies at assigned sites. The CRA monitors study conduct, ensures compliance with AZ Procedural Documents, ICH-GCP, and local regulations, and collaborates with investigators and site staff. The CRA may also contribute to study start-up, regulatory maintenance, and training.

The Country Study Manager delivers clinical studies in compliance with GCP and regulatory requirements. Responsibilities include site activation, monitoring, recruitment, and communication with study teams and regulatory authorities. Requires experience in clinical trial operations, GCP, and strong communication and organizational skills.

Senior Logistics Specialist to oversee global V2V logistics for cell therapy clinical trials across Europe and the UK. Responsibilities include depot operations, shipment management, vendor collaboration, and process improvement. Requires 5+ years of clinical logistics, cell therapy, or pharmaceutical supply chain experience.

Ensures timely and accurate submission of regulatory reports, including Adverse Event Reports and Periodic Safety Update Reports. Interprets and applies global regulatory reporting requirements and monitors guideline updates. Coordinates pharmacovigilance reporting activities, ensuring compliance with Good Pharmacovigilance Practices. Collaborates with internal and external teams to align on reporting needs and provide training on regulatory reporting obligations. Maintains knowledge of relevant country regulations, global and local guidance documents, and product safety obligations.