114 English-speaking jobs in Darmstadt

ABOUT THIS POSITION You would be joining a growing team of 4 colleagues and over 50 robots that are spread all around the globe. YOUR TASKS Working on the frontline with our customers and the product engineering team to ensure the successful (remote) deployment of the robots and our software solution, potentially at the customer's facilities.

ABOUT THIS POSITION As a Drone UI Full-Stack Engineer, you will play a crucial role in designing, developing, and maintaining both the backend and frontend components of our applications. You will work closely with our AI specialists, data scientists, and other developers to create robust, scalable, and high-performance solutions.

We're Celonis, the global leader in Process Mining technology and one of the world's fastest-growing SaaS firms. We believe there is a massive opportunity to unlock productivity by placing data and intelligence at the core of business processes - and for that, we need you to join us.

Reference ID : 41404 Are you looking for a working student job where you can do more than just watch? Or do you want to focus your thesis on something that is really in demand in the industry? Then Döhler is exactly what you're looking for!

We are! It’s our ambition to shape the future of nutrition. Döhler is a leading global producer of natural ingredients and solutions for the food, beverage, lifestyle and nutrition industries. We use innovative technology to process plant-based raw materials and enrich products such as lifestyle drinks, cereals, dairy, and confectionery goods for almost every well-known brand. Close to 10.

We are seeking a seasoned technical Product Owner with significant experience in the Data & AI domain to drive the product vision, strategy, and roadmap of our internally built Healthcare R&D knowledge graph. This role is pivotal to the success of our R&D efforts in discovering and developing new drugs.

As the Head of Cyber Protection, you play a pivotal role within the Electronics (EL) cyber security team, reporting directly to the EL CISO. You are part of the global cyber security team, interfacing with the EL business and corporate cyber security team. You lead teams managing identity and access controls, protecting endpoints, and ensuring effective response and recovery processes.

Join our seasoned and driven team, as a strategic partner to our senior business leaders & HR colleagues. You will be in the lead of executive recruiting for an entire division of the organization, globally.

As Senior R&D Data Scientist, you will facilitate the development, evolution and delivery of predictive and proscriptive analytic solutions, including an existing Bayesian causal inference model, to support study feasibility, operational planning and delivery of our portfolio.

Senior Corporate Patent Counsel We are looking for an experienced European or US patent attorney to strengthen our pharma patents team at our company in Darmstadt, Germany (Frankfurt area). As a member of cross-functional teams, you shape the global IP strategy for pharmaceutical development projects and commercial products.

*The role is field based and can be located either at the US East Coast or anywhere in Europe* As a member of Contract Testing Services (CTS) Leadership Team (LT) own the top line of the NA and EU P&L: Full responsibility for CTS Sales in two main regions, across all customer segments. Also contributes to CTS Strategy development and general decision making at CTS LT.

During the 24-month talent development program, you will experience a mix of strategic management consulting projects as well as functional rotational stations in the pharmaceutical, life science and performance materials industries.

In order to bring these business applications into the future, it is a key objective to modernize these systems and to offer a cost-effective operation. Software AG is planning to launch a new product that will modernize COBOL z/OS applications leveraging Java technologies on z/OS. Be you, join us.

In this role, you will collaborate with business partners from Electronics, subject matter experts from IT Application Technology, and other IT team members to guide and document high-level business needs and detailed requirements. You will define, lead, and implement improvements to business processes, ad-hoc projects, and support major ERP programs and projects for your domain.

As the Lead Expert Planning & Scheduling within the Life Science Engineering & Technology group, you will develop a governance structure for a global team focused on the planning and execution of capital projects. Projects in the Capital portfolio range from production expansion, equipment installation, and greenfield plant construction.

A great opportunity has opened within the Data Monitoring, Management and Innovation department to further strengthen our Clinical Data Management team. As a Senior Clinical Data Manager, you will play a crucial role in managing and overseeing clinical data management activities within the organization.

Collect business requirements concerning data-management and -analysis and translate this in the implementation strategy of scientific data management Collaborate closely with relevant stakeholders, e. g. IT, Scientific Experts, Technical Project Managers, , Quality function, Drug Product & Drug Substance internal and external Pharmaceutical manufacturing sites in Europe, Latin America and Asia.

As Process Manager Integrated Business Planning (IBP) involves joining the strategic initiative of the Life Science Integrated Business Management (IBP program at Life Science) team and working in a fast-paced, entrepreneurial environment. You'll support the Head of IBM Governance and Implementation in the rollout of the IBM framework at Life Science.

We are looking for an experienced Director Regulatory Affairs Medical Devices (all genders) who will be responsible for the regulatory strategy of our medical device business and leading the Regulatory Affairs team within Bioelectronics.

As a Principal Medical Writer you will play a pivotal role in leading the Medical Writing efforts for Marketed Products and Lifecycle Management, both globally and at regional/local levels. This includes independently preparing or overseeing the preparation of clinical and regulatory documents such as Protocols, Clinical Study Reports, Investigator Brochures, or Clinical Summary documents.