277 germany English-speaking jobs in Schleswig-Holstein

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.

Team Lead Assembly to plan, coordinate, and oversee daily assembly operations, ensuring safety, quality, and productivity. Develop, implement, and optimize processes to improve production efficiency. Collaborate with cross-functional departments and team leaders.

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.

Medpace, a global CRO, seeks an Entry-level Clinical Research Associate with Clinical Research Coordinator experience to support Phase I-IV clinical development services.

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.

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.

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, 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.

Director, Field Design The Director, Field Design is an enterprise leader with an entrepreneurial mindset and deep experience and expertise in development, measurement and optimization of customer facing resourcing and effectiveness.

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.

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 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.

Medical Lead - US Oncology The US Oncology Medical Lead is a key role within the US Oncology Medical Affairs (USMA) organization reporting directly into the Medical Head. The Medical Lead is accountable for supporting the development of the Medical strategy and initiatives for specific indications within biliary tract and pancreatic cancers.

Leads competitive analysis for Oncology R&D, shaping strategy and influencing investment decisions. Delivers insights on the evolving oncology landscape to Senior Leadership and partners.

Medical Science Liaison (MSL) for Neurology/Meta+ products. Provides scientific expertise to healthcare professionals and key opinion leaders, fostering scientific partnerships and supporting product strategies. Requires a Bachelor's degree, fluency in English, and 2-3 years of MSL experience (new graduates considered). Pharmacist license preferred.

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 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.

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.