770+ English-Speaking Jobs in Klein-Winternheim

KI-Beschreibung

You design experiments and analyze data on immune responses, present findings, and collaborate with a diverse team of scientists to advance research in personalized immunotherapies.

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  Master’s degree in related field
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  Experience in cell culture and immunological methods
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  Strong written and verbal communication skills in English

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development and execution of biomarker strategies in oncology, collaborating with various teams and external partners to ensure effective translational research and clinical implementation.

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  6 to 10+ years in oncology clinical development
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  Ph.D. or PhD/
  MD in immunology
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  Strong scientific background in oncology

Deine Vorteile

KI-Beschreibung

This program provides a unique opportunity for PhD candidates to engage in advanced research and development, promoting innovation and collaboration in a dynamic academic environment.

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  Master’s degree in relevant field
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  Good command of English

Deine Vorteile

KI-Beschreibung

You use advanced biochemical techniques to purify and characterize transcription factors and chromatin structures, while employing imaging and force spectroscopy methods to study their behavior.

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  Excitement about Condensation and Chromatin Biology
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  Very good oral and written communication skills in English
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  Experience with good scientific practices

Deine Vorteile

KI-Beschreibung

You manage legal liability assessments and ensure safety oversight for Comirnaty, while supporting regulatory documentation and collaborating with teams on post-marketing safety initiatives.

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  Medical Degree
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  3 or more years experience as physician
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  Good knowledge of German health insurance

Deine Vorteile

KI-Beschreibung

You will lead PBPK modeling efforts across various projects, enhancing decision-making through independent modeling and collaboration with cross-functional teams while ensuring regulatory compliance.

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  Several years in biotechnology or pharmaceutical industry
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  Strong knowledge of PK, PK/
  PD, PBPK, QSP modeling
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  Degree in pharmacokinetics or related field

Deine Vorteile

KI-Beschreibung

You oversee the development of quality documents and work with teams to ensure compliance with material requirements, focusing on RNA therapeutics and enhancing procurement processes.

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  Minimum 5 years in pharmaceutical or biotech
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  Profound knowledge of GMP regulations
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  Expertise in QbD approaches

Deine Vorteile

KI-Beschreibung

You manage regulatory documentation and coordinate with stakeholders to ensure compliance, support inquiries, track activities, and enhance internal processes.

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  Approximately 3 years professional experience in Regulatory Affairs
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  Vocational training in technical or pharmaceutical field
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  Fluent command of spoken and written English

Deine Vorteile

KI-Beschreibung

You facilitate requirement gathering and define functional needs for implementation, ensuring alignment with business processes and providing insights for data-driven decisions.

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  7–10+ years as a Functional Consultant
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  Proven experience implementing Veeva Network
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  Strong expertise in customer data management

Deine Vorteile

KI-Beschreibung

You will define best practices and develop scalable business process templates while serving as a liaison between operations and business. Your expertise in supply chain processes will enhance compliance and efficiency in ERP projects.

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  Minimum 5 years in global supply chain management
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  University degree in supply chain management
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  Strong ERP system and project management skills

Deine Vorteile

KI-Beschreibung

You handle customer inquiries and ensure timely responses while coordinating with internal teams to resolve issues and improve processes. Your role is essential for maintaining effective communication and access to systems.

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  Completed commercial or IT-related vocational training
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  Strong communication and organizational skills
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  High service orientation and enjoyment of customer interaction

Deine Vorteile

KI-Beschreibung

In this role, you guide clinical strategies and oversee the execution of clinical trials, ensuring alignment across development functions and managing safety assessments throughout the process.

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  M.D. with strong scientific background
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  Several years of relevant experience
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  Strong experience in monitoring trial data

Deine Vorteile

KI-Beschreibung

You provide expertise in upstream manufacturing processes, ensuring smooth transitions to downstream operations while collaborating with various teams and maintaining regulatory compliance.

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  Extensive experience in upstream processing technologies
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  Advanced degree in Biotechnology or related field
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  Strong problem-solving and analytical skills

Deine Vorteile

KI-Beschreibung

You manage the transition and implementation of manufacturing processes, ensuring compliance and quality across sites while collaborating with various internal and external partners to improve operations.

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  Extensive experience in downstream processing
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  Proven track record in process development
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  Experience in tech transfer and launch activities

Deine Vorteile

KI-Beschreibung

You oversee quality performance and audits at the site level, ensuring effective communication with global quality teams and supporting the implementation of quality initiatives.

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  At least 10 years of experience in quality management
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  University degree in a scientific field
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  Strong analytical skills

Deine Vorteile

KI-Beschreibung

You analyze and optimize quality processes, ensuring data integrity while collaborating with various teams. Your role includes leading digitalization projects and participating in interdisciplinary initiatives to improve efficiency.

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  3-5 years of practical experience
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  Bachelor's degree in Engineering Informatics
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  Proficiency in English, both written and spoken

Deine Vorteile

KI-Beschreibung

You provide analytical expertise for late-stage projects, ensuring compliance and managing method validation. Your role includes strategic discussions and timely evaluations for regulatory submissions, supporting successful product launches.

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  Industry experience of 5+ years in CMC development
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  Advanced university degree in a scientific discipline
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  Expertise in analytical control strategies and method validation

Deine Vorteile

KI-Beschreibung

You will provide scientific expertise in clinical safety, manage safety processes, and support cross-functional collaboration to ensure compliance with quality standards and regulations in safety management.

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  Minimum 5 years of experience in clinical research
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  Strong knowledge of regulatory and GCP requirements
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  Experience in clinical safety processes and tools

Deine Vorteile

KI-Beschreibung

In this role, you lead the design and execution of clinical trials, collaborating with industry partners and health authorities. You drive strategic planning and ensure high medical standards while mentoring a multidisciplinary team.

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  Minimum of 10 years in oncology drug development
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  M.D. with strong scientific background
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  Thorough understanding of clinical development methods

Deine Vorteile

KI-Beschreibung

You assist with various digital transformation projects, gaining insights into knowledge implementation and creating educational content within the human pharmaceutical industry.

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  Ongoing Master's study in relevant fields
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  Very good communication skills in English
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  Knowledge of data analytics tools

Deine Vorteile

KI-Beschreibung

You will oversee the design and implementation of legal and compliance processes, ensuring efficiency and adherence while collaborating with various teams to drive continuous improvement and optimize data usage.

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  Extensive experience in process management
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  University degree in Legal or Compliance
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  Fluent in English with international experience

KI-Beschreibung

You manage and monitor various initiatives to ensure effective project governance and deliverables. Your role includes data analysis and developing strategic solutions while keeping projects aligned with overall goals.

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  Several years experience with top-tier management consultancy
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  Master’s degree in sciences, economics or engineering
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  Proficiency in project management and MS Office

Deine Vorteile

KI-Beschreibung

You will oversee the clinical development of Vicadrostat-Empagliflozin, guiding strategy and team management to ensure scientific rigor while aligning with regulatory and commercial objectives.

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  MD or PhD with profound experience
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  Long-term experience in Clinical Drug Development
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  In-depth regulatory expertise

KI-Beschreibung

You will develop and implement a global content strategy for scientific communications, ensuring the timely delivery of high-quality information while managing budgets and fostering collaboration across teams.

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  Proven track record in Medical Affairs
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  Advanced scientific or clinical degree
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  Exceptional written and verbal communication skills

KI-Beschreibung

You drive strategic transformation in sourcing by analyzing trends and identifying opportunities for optimization. Your role involves managing demand and leading cross-functional projects to improve service delivery and performance.

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  Master’s degree in relevant field
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  Several years of sourcing experience
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  Proven project management track record

KI-Beschreibung

You will develop and implement innovative coating systems while testing new products and optimizing existing ones. Your role includes project planning, field testing, and acting as a technical advisor.

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  Master's degree in chemistry or related field
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  Professional experience in electroplating
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  Profound expertise in technical chemistry

KI-Beschreibung

You manage the administration and preparation of test vehicles, support software validation, and conduct various system tests to ensure efficient handling of data and equipment.

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  Owner of EU driving license B - mandatory
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  Technically skilled student with university enrollment
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  Good command of English language

KI-Beschreibung

You analyze system requirements and develop test cases for IVI systems, ensuring quality through audits and collaboration with partners. Your role includes tracking issues and suggesting improvements to enhance performance.

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  At least two years' experience in System validation
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  Driving test experience in EU region
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  Bachelor's or Master's in Computer Science

KI-Beschreibung

You develop and implement simulation models to evaluate energy efficiency, analyze results for optimization, and collaborate with various teams to integrate energy management strategies into vehicle performance.

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  >3 years’ experience in automotive industry
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  Degree in mechanical engineering or related field
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  In-depth understanding of powertrain behavior

KI-Beschreibung

You will provide medical writing expertise for HTA projects, collaborating with various teams to ensure timely document preparation and compliance with EU regulations while maintaining quality and addressing any challenges in the writing process.

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  Minimum 3 years in bio-pharmaceutical industry
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  Extensive experience writing HTA dossiers preferred
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  Bachelor's Degree or higher in scientific discipline