257 germany English-speaking jobs in Schleswig-Holstein

This senior manager role within Global Supply Planning is responsible for creating, developing, and maintaining cross-brand supply & capacity plans. The role drives the S&OE process, facilitates meetings, and ensures executable supply plans are handed over to manufacturing locations. Key responsibilities include supply execution, S&OE facilitation, KPI tracking and reporting, inventory management, and capacity plan updates.

As a Principal Enterprise Architect in Sustainability, you will develop architecture standards, technology strategies, and roadmaps to support AstraZeneca's sustainability mission. You will provide enterprise design thinking across various domains, lead architecture assessments and reviews, and support solution development efforts.

Coordinates Clinical Data Management deliverables on assigned studies, serving as the main point of contact for the Data Management vendor. Ensures deliverables follow standards and meet data quality. Provides guidance and supervision to the Lead Data Manager/DM Team Lead. Oversees vendor timelines, deliverables, and performance. Maintains awareness of industry trends and participates in continuous improvement activities.

The Manager, Global Clinical Solutions coordinates and leads the delivery of services and technology to support AstraZeneca's Clinical Development programs. This role provides expert support to user communities, conducts process analyses, and leads continuous improvement projects. The Manager also serves as a co-Project Manager for eCOA and DPS setup, maintenance, and closure.

Associate Director, Strategic Projects and Organisational Enablement supports CMO leaders in strategic planning and execution of goals. Oversees sub-department budgets, performance improvement projects, and cross-functional collaboration. Leads business planning, stakeholder management, and communication strategies. Requires a Bachelor's degree, 5+ years of industry experience, and proven success in driving strategic initiatives and business improvements.

The Director, Safety Scientist leads risk management evaluation and resolution for assigned products and projects. Responsibilities include organizing and mentoring safety scientists, co-leading activities related to regulatory filings, and representing global patient safety at inspections. Requires an advanced degree in a biologic/medical/clinical/nursing field with at least 7 years' experience in drug safety and risk management.

Develop and implement Brand Strategic Plans, including market share and sales targets. Gather and interpret market analyses, SWOT, competitor analyses, and sector developments. Lead strategic decisions to enhance business performance.

Senior Statistical Programmer provides programming support and leads activities related to the analysis and reporting process for clinical studies. Responsibilities include clinical study report development, regulatory submissions, and the scientific utilization of data. Requires a Bachelor's or Master's degree in a relevant field and at least 3 years of industry experience. Extensive SAS programming expertise and knowledge of CDISC standards are essential.

Leads phase-appropriate formulation and process development for injectable biologics, from candidate selection through commercial validation and filings. Designs, executes, and troubleshoots laboratory studies using advanced biophysical and analytical methods. Defines and optimizes drug product processes, conducts scaleup and robustness studies, and supports technology transfer. Integrates complex datasets to establish structure–function relationships and translate insights into robust formulations and control strategies. Authors protocols, technical reports, and contributes to CMC sections of regulatory submissions.

Leads the development and implementation of global regulatory strategies for assigned portfolios, ensuring alignment with organizational goals and regulatory requirements. Provides expert strategic direction throughout the product lifecycle, from pre-approval through post-marketing activities. Serves as the primary contact for health authorities and manages interactions with external stakeholders. Collaborates with senior leadership and cross-functional teams to provide regulatory insights and inform drug development strategy.

Leads a team delivering compliant, efficient contracting and coordination for healthcare providers and patient engagements. Owns operational performance, ensures adherence to AstraZeneca policies, and builds data-driven insights. Partners across functions to drive adoption of the E3S operating model and improve processes.

Leads a team of Synthetic Chemists in developing synthetic manufacturing processes for small molecule drug substances. Responsible for process development, scale-up, control strategy development, technology transfer, and regulatory submissions. Manages a team of Synthetic Chemists, including coaching, mentoring, and performance management. Contributes to the Chemistry development strategy and drives continuous improvement within the function.

Leads a group of submissions or programs, overseeing communication strategy and driving the use of drug and disease-specific knowledge. Develops and optimizes communication strategies, content, and processes across multiple programs or submissions. Authors and reviews key submission documents, ensuring consistency of messaging. Represents Clinical Regulatory Writing on improvement workstreams and external activities. Supports recruitment and onboarding activities. Minimum Master's degree in a scientific discipline required, PhD preferred. Proficiency in authoring/editing and managing clinical regulatory documents and submissions. Thorough understanding of oncology drug development and knowledge of oncology endpoints required. Experience in program management and effective communication with stakeholders.

Establishes and executes strategy for a major oncology brand, aligning with global sales and marketing objectives. Manages resource allocation, ensures operational efficiency, and leads a team of senior managers. Requires a degree in a relevant subject and mastery of brand management.

The Associate Director Clinical Research delivers clinical interventional studies, manages staff, and ensures study site compliance with regulations and guidelines. Requires a bachelor's degree, minimum 4 years of relevant experience, and strong leadership, communication, and project management skills.

Leads the digital transformation of packing operations, developing and executing digital strategies to improve speed, quality, and efficiency. Manages digital projects, identifies emerging technologies, and champions a culture of digital innovation. Requires experience in packing processes, program management, and communication across all levels.

QC Analyst will perform lab functions in compliance with cGMP, following written procedures for various tests including electrophoresis, HPLC, and protein concentration methods.

Designs and implements strategic brand initiatives for the rare disease sector. Develops local brand strategies, conducts market analysis, and manages marketing campaigns. Collaborates with cross-functional teams to ensure unified brand messaging and successful strategy execution.

As an SAP Tax Consultant, you will define the global template for AstraZeneca's indirect tax processes within the Axial Programme. You will work on the IT design team to ensure integration between business processes, SAP solutions, and data objects. You will also document, test, and guide the design through governance forums.

Senior District Business Manager will develop and execute district operational plans, drive brand plan execution, and analyze district performance. The role requires a minimum of 2 years in the position, sales performance above 90% or national performance, and a DBM Proficiency Level rating of at least 3.5.