262 English-speaking jobs in Schleswig-Holstein

Sell industry-leading printing solutions with an unmatched commission structure. Earn 90% profit share on the first 3 printer equipment sales, thereafter 75%. Receive 50% of the profit from ongoing service contracts. Identify and engage potential clients, develop relationships, and provide expert consultation.

Support the cleanliness and hygiene of office environments, including bathrooms and shared spaces. Duties include cleaning office areas, kitchens, and bathrooms, vacuuming, emptying waste bins, and refilling consumables.

Sell industry-leading printing solutions on a flexible basis. Earn a 90% profit share on printer equipment sales and 50% of ongoing service contract profits. Develop client relationships and close deals on hardware and managed print services.

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.

Sales Consultant to identify and engage new business clients for print and document solutions. Build relationships, conduct needs assessments, and close deals on hardware and service agreements. Maintain client relationships and identify upsell opportunities.

Promote managed print and hardware solutions to business clients. Develop long-term client partnerships and secure equipment and service agreements.

Develop novel high-throughput in vitro assays to screen small molecules that modulate RNA–protein interactions. Design, execute, and validate assays using technologies like TR-FRET and AlphaLISA. Contribute to innovative research in RNA-targeted drug discovery.

Leads complex process re-engineering projects, analyzes and redesigns business processes, and manages relationships with stakeholders.

Associate Director, GCS Delivery, Solutions Implementation Lead provides technology support and manages clinical technologies for global studies. Leads technology implementation, end-to-end process management, and cross-functional collaboration. Requires a university degree in a relevant field and significant experience in clinical research.

The Study Contract Manager drives costings and contracts for clinical trials, negotiating and budgeting with investigators, institutions, and vendors. Responsibilities include adapting agreements to local requirements, ensuring contract integrity, and managing study budgets and payments.

The Clinical Transparency & Data Sharing team seeks an Analyst to anonymize clinical study documents and data for regulatory submissions and data sharing. The role requires expertise in anonymization techniques, clinical study datasets, and regulatory policies. The Analyst will work with study teams globally to deliver anonymized documents and contribute to anonymization reports.

Data & Advanced Process Analytics Engineer will develop process models, build dashboards, and leverage AI/ML to drive process performance improvements. Requires a degree in Computer Science, Data Science, or related field, 1-3 years of data & analytics experience, and strong SQL and visualization skills.

Leads cross-functional study teams to ensure clinical study progress according to timelines, budget, and quality standards. Manages study level documents, external service providers, and study budgets. Provides guidance and mentoring to less experienced colleagues. Requires a university degree in medical or biological sciences, at least 7 years of clinical trial experience, and at least 3 years of global study leadership experience. Demonstrated clinical trial expertise in hematology and/or oncology is required. Extensive knowledge of ICH-GCP guidelines and clinical research regulatory requirements is also needed.

Product Manager for AI Authoring will bridge clinical trials, medical writing, and AI technology to create innovative solutions for the pharmaceutical industry. Responsibilities include strategic product thinking, execution and delivery, user research and experience, design and rapid prototyping, stakeholder engagement, and AI & innovation.

Physician scientist will lead AI research programs, leveraging clinical expertise and AI knowledge to drive innovation in drug development. Requires MD and 3+ years clinical experience plus 3+ years leading AI for health research programs, including 2+ years in generative AI.

Global Medical Insights & Analytics Director will partner with therapeutic area medical teams to develop medical strategies and KPIs. Drive data collection, analysis, and reporting to monitor medical strategic alignment, performance, and impact. Leverage expertise to drive programs that inform medical performance and influence the design of medical platforms.

Leads a global team of occupational toxicology experts, providing strategic advice and ensuring compliance with scientific quality and regulatory standards. Develops health-based exposure limits, authoring documentation for regulatory compliance and supporting product quality and worker health and safety. Provides toxicology support for nonclinical safety assessments and prepares toxicology assessments for Safety Data Sheets. Implements risk management processes for employee health hazard assessments and manages occupational testing programs.

Leads and manages a team of statisticians, providing biometrics support and strategy for drug projects. Develops and implements statistical innovation, including leading-edge methodology and best practices.

Develop and benchmark in-solution affinity measurement techniques for drug discovery. This master's thesis involves experimental design, cell culture, assay development, and data analysis.

The Product Technical Lead provides company-wide technical leadership for assigned (bio)pharmaceutical products throughout the product lifecycle. Responsibilities include maintaining product process knowledge, leading product improvement roadmaps, and serving as a technical liaison across functions to ensure regulatory compliance and technical manufacturing excellence. The role requires a Bachelor's degree in a scientific or engineering subject area with experience in (bio)pharmaceutical manufacturing/development/process engineering and a demonstrated ability to lead cross-functional teams.