3040 marketing germany English-speaking jobs in Hesse

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.

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 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.

experienced European or US patent attorney to strengthen our pharma patents team at our company in Darmstadt, Germany ... established team of patent attorneys with global responsibility, reporting to the Head of Patents Healthcare Germany

The Global Business Services (MBS) Trainee Program offers a comprehensive 24-month rotational experience within our Shared Service Center in Darmstadt. Throughout the program, trainees will have the opportunity to engage in diverse projects, both locally and abroad, and gain exposure to senior management.

*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.

The Procurement End-to-End Process Owner (E2EPO) is a dynamic and strategic role designed for leaders who thrive in optimizing complex business processes.

your network and gain in-depth knowledge in the day-to-day operations of different functions, such as marketing

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.

You will be part of a combined team of Merck and an external service provider that is responsible for process automation. Your tasks will includeall areas of Automic/UC4 system administration (installation, configuration, performance tuning, disaster recovery planning / testing, life cycle management etc. ),design of complex scheduling processes (incl.

degree or Ph.D. preferred.5 to 8 years of regulatory medical writing experience, with a focus on post-marketing

You will be part of the Process Solutions Supply Chain team which is managing product portfolios across the globe.

understanding in the areas of Finance, Order-to-Cash (O2C), Source-to-Pay (S2P), or Healthcare Compliance (Marketing

As a Working Student in our Data Science Team, you can play a key role in how we develop, operate, and scale innovative data-driven solutions for our customers in the semiconductor industry. You will research and implement state-of-the-art conformal prediction methods to address data science challenges in critical manufacturing processes and improve the robustness of our machine learning models.

Location: Flexible, Darmstadt, Germany or US preferred Key Responsibilities:Define, implement, and maintain