292 English-speaking jobs in Schleswig-Holstein

PLC Development and Support Engineer will design Beckhoff PLC programs (TwinCAT3) and safety programs (TwinSAFE), test and commission systems, and provide support for installed systems.

Global Study Manager to oversee international haematology studies from early development through late phase. Responsibilities include protocol development, vendor management, budget oversight, and ensuring compliance with ICH-GCP and global regulations. Requires 5+ years of clinical research experience, 3+ years of project management experience, and experience in haematology. Must have experience applying AI or automation in Clinical Operations. Fluent English required.

UX Content Designer will collaborate with cross-functional teams to design user-centric content for web and mobile platforms. Responsibilities include designing content experiences, contributing to content strategy, and maintaining the Content Design System. Must have at least 3 years of experience as a UX Writer or Content Designer and excellent writing proficiency in English. Proficiency in German, Spanish, Italian, or French is a plus.

Brand Manager for Respiratory & Immunology therapeutic area. Develops, executes, and implements strategic plans and activities for brand success. Requires 3+ years pharmaceutical experience, 1+ year as a brand manager in Europe, and a higher medical education. Excellent communication and analytical skills are essential.

The Patient Centricity Lead will embed patient perspectives into organizational activities and strategies. This role will build partnerships with patient organizations, incorporate patient insights into product development, and drive initiatives to enhance the patient experience.

The Medical Science Liaison (MSL) specializes in Oncology and provides scientific support to Key Opinion Leaders (KOLs). The MSL establishes and maintains expert collaborations, identifies partnership opportunities, and communicates scientific information.

The Country Study Manager is responsible for the delivery of clinical studies in compliance with GCP and regulatory requirements. The role involves collaborating with internal teams to ensure timely and efficient study execution, interacting with regulatory authorities, and managing site activation and monitoring activities. The CSM ensures quality and timeliness of study deliverables, proactively reports issues, and drives performance at the sites.

The Senior Manager Traceability leads product traceability and serialization activities within the Alexion AstraZeneca Rare Disease Unit, ensuring compliance with global standards and regulatory requirements. This role involves developing, implementing, and testing traceability systems, processes, and standards, as well as providing day-to-day operational support. The Senior Manager Traceability will collaborate cross-functionally to manage alerts, audits, and security features, and represent Alexion in brand launch projects and industry working groups.

The Principal Investigator plans, executes, and manages assigned clinical trials. Responsibilities include mentoring staff, conducting trials according to protocols and guidelines, managing risks, and ensuring data accuracy and patient safety.

HR Organizational Enablement Manager will design people strategies and structures to support global growth. Responsibilities include M&A integration, plant network optimization, project execution, organizational design, change management, and talent development.

Regulatory Reporting Advisor - Patient Safety will prepare, review, and submit regulatory reports, ensuring accuracy and compliance. The role involves literature surveillance, reportability decisions, and collaboration with cross-functional teams. Experience in regulatory affairs, pharmacovigilance, or regulatory reporting in the pharmaceutical industry is required.

Supply Chain Coordinator manages import/export, customs clearance, and shipment distribution for pharmaceutical products. Requires a Bachelor of Pharmacy and 3+ years of experience in pharmaceutical operations or a related science field. Must have fluency in English and experience with EDA/NODCAR processes, cold-chain logistics, and distributor audits.

The Associate Director of Market Access Insights supports Market Access customer-facing teams by compiling and evaluating customer performance metrics and market analysis to guide brand strategies. This role requires strong influence without authority, a deep understanding of the Market Access landscape, and collaboration with various internal and external stakeholders.

Provides technical support and administrative assistance for a specialist area within a field of activity. Processes technical documents, conducts procurement, and maintains device databases. Requires vocational training, experience in the field, and strong Excel skills.

This HR Performance and Portfolio Analyst role focuses on data strategy, ROI measurement, and governance within the HR organization. The position supports the annual HR planning cycle, develops performance dashboards, and ensures data integrity.

Leads the implementation of strategic vision for biomarker development in hematology drug discovery and development programs. Delivers biomarkers for clinical studies and guides indication selection and patient stratification. Collaborates with clinical development and research teams to implement translational strategies and manage research collaborations. Requires a PhD and/or MD with oncology drug development experience and in-depth knowledge of hematology disease area biology.

The Associate Director, Safety Scientist, Global Patient Safety evaluates and manages risk for multiple product portfolios. Responsibilities include managing safety scientist activities, supporting regulatory filings, and leading gap analysis. Requires a bachelor's degree in a biologic/medical/clinical/nursing field and 5+ years of drug safety experience.

Leads AstraZeneca's AI strategy for Discovery Sciences, applying AI and machine learning to accelerate oncology and biopharmaceutical R&D. Develops and owns the enterprise AI strategy for Discovery Sciences, spanning target identification/validation, compound optimization, mechanistic modeling, and hypothesis generation. Guides, partners, and leads strategies and initiatives at the highest levels within AstraZeneca Discovery Sciences. Serves as a thought leader and advisor to Discovery Biology, Discovery Chemistry, Translational Medicine, and Therapeutic Area leadership on AI applications. Builds and leads a high-performing global organization promoting rigor, innovation, and collaboration.

The Senior Clinical Programmer I designs, develops, and validates sophisticated programs in SAS/Python/R or dashboard applications such as PowerBI/Spotfire for ongoing clinical studies. Responsibilities include processing, analyzing, and reporting clinical trial data, contributing to complex projects, and providing technical expertise to ensure high-quality deliverables.

Leads the development and delivery of production-grade analytics and ML solutions that guide medical strategy and accelerate decisions. Builds, assesses, and deploys ML models for predictive analytics, classification, regression, NLP, and time-series forecasting. Develops web-based UIs, dashboards, and decision-support tools. Manages a team of data analysts, data scientists, and application engineers. Translates business needs into technical requirements and ensures solutions meet data governance, privacy, and security standards. Evaluates new technologies and proposes POCs and new analytics capabilities.