3270 SAP germany English-speaking jobs in Hesse

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.

The RDQ Quality Strategy Lead (all genders) Development will be mainly responsible for managing clinical programs day to day activities from quality assurance perspective and delivering the full range of quality related activities in support of the program.

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.

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

We are seeking a Senior Data Standards Expert to join our dynamic Data Standards & Integration team within the Data Monitoring, Management and Innovation department. As a Senior Data Standards Expert, you will utilize your extensive knowledge of CDISC standards including CDASH, SDTM, and ODM-XML to support our diverse clinical development portfolio.

As the company's internal consultancy, we drive projects across all our business sectors, ranging from Healthcare to Life Science, Electronics, and Group Functions. Our approx.

Product Quality Lead (PQL) is responsible for providing quality oversight of Pharma products/franchises throughout the product and design control lifecycle. Develops, approves, monitors, and maintains critical quality standards to proactively minimize product quality and design control risks.

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.

Your roleAs a Senior Scientist, Computational Biology within the Research Unit Neuroscience & Immunology (N&I), you will join a team of highly motivated scientists dedicated to discovering the treatment solutions of tomorrow for autoimmune & neurodegenerative disorders.

We are offering an exciting opportunity in Corporate Strategy, where you will join us in unlocking our full potential to take the company to the next level. As part of an enthusiastic, vibrant, and growing team, you will drive the ompany's strategy development, portfolio, and M&A strategy, as well as the execution of strategic projects and initiatives.

As a working student in data culture at Healthcare, Darmstadt, Germany, you will have the opportunity

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.

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.

The Materials Innovation Pipeline (MIP) seeks a curious, open-minded synthetic chemist who is experienced in advanced metalorganic chemistry. In line with Electronics mission to Advance Digital Living, MIP imagines and creates sustainable solutions and novel products for the semiconductor industry.

starting September 01, 2024; A valid work permit is required for the internshipLocation: Darmstadt, Germany

(Senior) Internal Auditor Operational Audits (all genders) We're seeking highly motivated individuals to join our dynamic, diverse, and very engaged internal audit team! We offer a high-profile internal audit function, with good visibility on all management levels and a track record for developing employees into senior roles in finance and business.

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.