238 English-speaking jobs in Schleswig-Holstein

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. Develops and maintains study plans, manages budgets, and mentors team members.

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.

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.

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.

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.

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.

Manages clinical trials and publications, collaborating with CROs, investigators, and internal teams. Ensures study conduct aligns with AZ procedures, SOPs, and regulations. Oversees site/investigator selection, budget preparation, and protocol development. Requires a degree in a related field and experience in clinical trials, observational studies, and publications.

Regulatory Affairs Manager ensures adherence to industry codes and maintains product licenses. Develops and implements regulatory strategies for product approvals and launch. Provides guidance to the regulatory team and monitors the regulatory environment. Manages legal and patent-related matters and acts as Company Pharmacist.

Leads Local Study Teams to deliver clinical studies, ensuring compliance with AZ Procedural Documents, ICH-GCP, and local regulations. Manages site selection, initiation, monitoring, and closure. Oversees study budgets, documentation, and drug activities. Reports study progress and collaborates with internal and external stakeholders. Requires a Bachelor's degree and 3+ years of experience in clinical trial coordination, with a focus on Oncology.

Technical Sales Engineer will support customers across Europe with sensing and geospatial technology solutions. The role involves translating client needs into effective solutions, conducting product demonstrations, and providing technical support. Requires a Bachelor's degree in a relevant field and 3 years of experience in surveying, geospatial, GPR, or engineering.

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.

Senior Project Manager will support Regional Tumor Teams (RTT) across the EUCAN region, ensuring alignment with business unit and company objectives. Responsibilities include driving in-market performance, executing regional launches, and managing operational support for RTTs.

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.

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.

Leads the data science strategy for Vaccines & Immune Therapies, defining and delivering solutions across clinical and operational domains. Manages a team of data scientists, partners with stakeholders, and champions best practices in model development and data governance.

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.

Leads global cell therapy clinical operations, defining strategy, ensuring regulatory compliance, and overseeing trial execution across multiple indications and geographies. Builds and manages a global team, develops site networks, and partners with stakeholders to deliver high-quality trials.

The GxP Quality, Compliance and Audit Associate Director will develop, implement, and improve Evinova's Quality Management System, ensuring alignment with global regulatory standards. This role will guide teams on applying GxP principles, plan and lead internal audits, and oversee supplier and third-party qualification and audit activities.

Leads the development and implementation of oncology business unit strategies, integrating into a company-wide oncology strategy. Drives portfolio strategic initiatives, provides insights-driven valuations and strategies to C-Suite leaders, and manages a team of directors and associate directors.