222 germany English-speaking jobs in Schleswig-Holstein

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

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 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 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.

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.

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.

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.

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 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.

The Senior Project Planner will define and manage the integrated Technology project plan, provide planning updates to senior management, and support stage gate readiness.

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.

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.

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.

Manages and develops all supply chain functions within a factory to achieve production and business goals. Leads end-to-end supply chain operations, including production planning, material management, warehousing, and logistics.

Hospital Network Executive to build rapport with healthcare professionals, develop hospital listing plans, and execute sales strategies in assigned territory. Requires a Bachelor's degree in Pharmacy or Medical Science and 2-5 years of experience in medical sales.

As Lead Consultant for Cloud Networking, you will design and build cloud network architectures across AWS, Azure, and GCP, integrating them with on-premises environments. You will develop automation workflows, ensure compliance-by-design, and participate in the Network Architecture Review Board to maintain high-quality standards.

Define and deliver analytical strategies and control strategies for peptide, oligonucleotide, and other new modality drug products. Develop, optimize, validate, and transfer analytical methods; apply risk-based approaches to ensure method robustness and lifecycle stewardship. Author and contribute to regulatory filings and prepare high-quality responses to regulatory queries. Collaborate with process chemists, formulators, engineers, project leads, regulatory professionals, quality assurance, and external partners to achieve successful project delivery. Provide technical expertise and drug development experience to establish and optimize commercial supply for AstraZeneca development projects. Champion data-centric ways of working, leveraging digital tools, modeling and simulation, and emerging AI-enabled approaches to enhance robustness, efficiency, and decision-making. Lead root-cause investigations for out of specification (OOS), out of trend (OOT), and deviations; define effective corrective and preventive actions (CAPA). Uphold cGMP, SHE, and data integrity standards; foster a culture of quality and continuous improvement.

Leads and coordinates pre-clinical transactions, including research collaborations, partnerships, and licenses. Manages deal negotiation and closure, collaborating with cross-functional teams. Builds external networks within the biotech and pharmaceutical industry.

The Director, Business Planning & Operations for Cancer Biomarker Development will be a strategic partner to the VP, leading business cases, resource planning, and operational excellence. This role requires a Bachelor's degree and 7+ years in drug or biomarker development, with experience in business case development, project/program management, and operational leadership.

Integrate complex data into actionable insights and drive CRM, omnichannel, and CX capability uplift across Alexion ANZ. Translate analytics into recommendations for marketing, sales, and leadership. Improve CRM processes, data quality, and adoption. Collaborate across Commercial, Medical, Finance, IT, and Global teams.