228 germany English-speaking jobs in Schleswig-Holstein

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.

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.

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.

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.

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.

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.

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.

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.

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.

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 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 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.

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.

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.

Develops and enhances relationships with healthcare professionals, drives scientific initiatives, and coordinates medical activities to advance clinical practice.