KI-Beschreibung

As a Clinical Trial Manager, you will play a vital role in overseeing the operational and administrative aspects of clinical trials. Your day-to-day responsibilities will include preparing status reports, managing budgets, and coordinating activities with various teams to ensure successful trial execution.

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  Natural/
  life sciences or medical background
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  Minimum 3 years of experience in project management, regulatory submissions, monitoring of clinical trials or clinical trial coordination
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  Profound knowledge of relevant legislation and international guidelines (ICH-GCP)

KI-Beschreibung

In this role, you will navigate the complexities of regulatory affairs for diagnostic and medical device products, ensuring compliance while driving market access. Your expertise will be crucial in managing submissions and adapting to evolving regulations.

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  Relevant higher education (Master's degree or PhD) or extensive professional experience (typically >5 years)
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  Proven experience in regulated, quality-controlled environments
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  Skilled in preparing and assembling regulatory documents

Deine Vorteile

KI-Beschreibung

In this role, you will support the Cancer Vaccines Team by monitoring laboratory mice and assisting with various immunological assays, while ensuring compliance with animal welfare regulations.

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  Enrollment in a degree program in biology, chemistry, medicine, or a similar field
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  Willingness to work with laboratory animals (mice)
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  Relevant certification (e.g., FELASA Function A, FELASA Function C/
  D, or equivalent) advantageous

KI-Beschreibung

In this role, you will lead global regulatory efforts for development projects, shaping strategies for interactions with health authorities and overseeing the preparation of essential regulatory documents. Your expertise will help navigate the evolving regulatory landscape and ensure successful product authorization.

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  University degree in natural sciences or equivalent
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  9+ years of working experience in Regulatory Affairs
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  Experience in development of antibody- and ADC-based cancer therapies

KI-Beschreibung

In this role, you will drive complex projects and strategic initiatives, enhancing operational efficiency across drug development. Your day-to-day responsibilities will involve collaborating with senior leadership and fostering innovation within diverse teams.

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  Advanced degree (PhD, PharmD, MD, or MSc) in Life Sciences, Medicine, Pharmacy, or related field
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  Over 5 years of proven experience leading cross-functional teams
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  Expert knowledge of pharmaceutical drug-development processes

KI-Beschreibung

As a Capture & Level Artist, you will creatively shape the presentation of Anno 117: Pax Romana by capturing stunning in-game footage and translating creative briefs into engaging visual content, while also anticipating future marketing needs.

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  2+ years of professional experience as a Level Artist, Capture Artist, or similar
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  Experience with camera sequences, sequence editing workflows, scene staging, and video capture within modern game engines and development tools
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  Hands-on experience with video editing software (e.g., Adobe Premiere, After Effects, or similar)

Deine Vorteile

KI-Beschreibung

In this role, you will lead a team of medical writers, ensuring the creation of high-quality scientific documents while managing compliance with regulations. Your day-to-day responsibilities will include coordinating writing tasks, mentoring team members, and driving process improvements to support the development of novel therapeutic agents.

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  >10 years hands-on experience in drug development in therapeutically relevant field, preferably oncology or immunology
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  >10 years hands-on experience as scientific or medical writer in pharmaceutical/
  biotech industry
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  Relevant life science university degree, ideally M.D., Pharm. D, or Ph.D.

KI-Beschreibung

In this role, you will lead compliance efforts across Global Technical Development, ensuring training alignment and audit readiness while developing frameworks that support GxP requirements. Your expertise will help maintain data integrity and drive continuous improvement initiatives.

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  Master’s degree in pharmacy, Chemistry, Life Sciences, or related field
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  5+ years in pharmaceutical development, process improvement, or compliance
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  Deep understanding of global GxP requirements and regulatory frameworks

Deine Vorteile

KI-Beschreibung

In this role, you will drive innovation in cancer vaccine research by developing bioinformatics pipelines and collaborating with multidisciplinary teams. Your work will focus on analyzing transcriptomic data and ensuring data integrity to support groundbreaking research.

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  PhD in Bioinformatics, Computational Biology, or related field
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  Proven experience in transcriptomic analyses and development of bioinformatics pipelines
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  Strong programming skills in Shell scripting, R, and/
  or Python

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development of protein-based therapeutics and ADCs, collaborating closely with internal teams and external partners. Your focus will be on ensuring regulatory compliance, managing timelines, and driving continuous improvement in purification and bioconjugation processes.

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  Master’s degree or PhD in Biotechnology, Bioprocess engineering, Biochemistry, or comparable field
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  At least 5 years of relevant professional experience
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  Broad experience in protein (mAb) and ADC DS process development and manufacturing

Deine Vorteile

KI-Beschreibung

In this role, you will play a crucial part in product development and regulatory submissions for RNA and protein-based therapeutics. You will ensure that analytical methods meet GMP standards while collaborating with cross-functional teams and external partners.

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  Advanced university degree in a scientific discipline
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  Industry experience in CMC development/
  commercial
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  In-depth knowledge of analytical techniques with hands-on experience in assay development and validation

Deine Vorteile

KI-Beschreibung

In this role, you will leverage your scientific expertise to enhance clinical safety programs, analyzing safety data and leading safety surveillance efforts. Your daily responsibilities will involve collaborating with cross-functional teams and mentoring colleagues on best practices in safety management.

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  Minimum 5 years of experience in clinical research and pharmacovigilance
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  Advanced Degree in life sciences, pharmacy, public health, or related field
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  Strong knowledge of regulatory, GCP, and GVP requirements

KI-Beschreibung

In this role, you will oversee the execution of the ESM roadmap, ensuring that strategic initiatives progress smoothly while collaborating with various teams to enhance operational efficiency in delivering cancer treatments.

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  7+ years of profound experience in portfolio management, program management, project management, or IT strategy execution
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  Academic degree in computer science, information technology, business administration, management, or similar
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  Experience working in Enterprise Service Management (ESM), ITSM, or ServiceNow portfolio management

Deine Vorteile

KI-Beschreibung

As a Driver/Data Collector, you will be on the move capturing high-quality visuals of streets and key locations. This role involves using advanced equipment to gather data that enhances a leading online mapping platform, ensuring every detail is documented.

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  At least 5 years of driving experience
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  Valid EU-issued driver’s license
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  Professional driving experience (e.g., taxi, delivery, logistics)

Deine Vorteile

KI-Beschreibung

In this role, you will shape the digital experience by aligning the vision and goals for capabilities while collaborating with stakeholders to meet business needs. Daily responsibilities include managing platform changes, supporting training, and ensuring system performance.

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  Minimum of 5 years of work experience within business and/
  or IT roles in Tech, Pharma, Digital Agency, or Consultancy Services
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  Proven track record as Digital/
  Technical Product Owner, preferably within experience management systems (CMS, Commerce, or event solutions)
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  Knowledge of Adobe Experience Cloud, SpotMe, Cvent, Qualtrics, Figma, and Frontify

Deine Vorteile

KI-Beschreibung

You oversee the development and implementation of digital solutions, ensuring they align with business goals while facilitating change and maintaining system performance and security.

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  Several years of proven experience with Veeva systems
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  Ability to translate business needs into technical requirements
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  Strong analytical and problem-solving skills

Deine Vorteile

KI-Beschreibung

You collaborate with various stakeholders to define solutions and manage service delivery, ensuring alignment with digital strategies while supporting change management and training initiatives.

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  Proven experience with IPaaS systems
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  Hands-on experience with MDM rollout projects
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  Completed studies in Business Informatics

Deine Vorteile

KI-Beschreibung

You manage EU CTA submissions and ensure compliance with regulatory processes. Your role includes improving workflows, supporting governance structures, and providing training to enhance user understanding of the systems.

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  Minimum of 5 years experience in pharmaceuticals
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  Degree in pharmacy or equivalent
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  Sound understanding of EU-CTR processes

Deine Vorteile

KI-Beschreibung

You manage communication and lead technology transfer projects while ensuring that analytical methods are current. Your role includes problem-solving, overseeing documentation, and supporting continuous improvement in laboratory processes.

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  Several years of experience in biotechnology
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  Experience in leading analytical transfers
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  Knowledge in analytics of therapeutic proteins

Deine Vorteile

KI-Beschreibung

As a Product Manager for the Satcom Portfolio, you lead product development and strategy, ensuring they align with market needs and drive innovation in satellite communication solutions.

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  Leading and supporting various teams
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  Creating a network of contacts
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  Definition of concepts for products

KI-Beschreibung

You play a crucial role in coordinating the setup and maintenance of the IRT system, managing budgets, and supporting user training, while ensuring effective communication with vendors and maintaining essential documentation.

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  Bachelor’s degree in relevant field
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  Minimum 3 years of experience preferred
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  Knowledge of clinical supply chain processes

Deine Vorteile

KI-Beschreibung

You lead the design and execution of clinical trials, ensuring safety and regulatory compliance while collaborating with various teams to drive innovative drug development strategies.

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  M.D. with strong scientific background
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  Several years of experience in Immuno-Oncology
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  Thorough understanding of clinical development methods

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 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

In this role, you will embark on a development program designed to fast-track your career, gaining valuable insights across business areas while collaborating with enthusiastic teams on impactful projects.

Deine Vorteile

KI-Beschreibung

In this role, you will support the RDE team by processing emissions data and assisting with various testing activities. Your day-to-day responsibilities will involve working with EV vehicles, managing databases, and contributing to measurement campaigns.

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  Valid European driving license B
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  Technical background and passion for cars
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  Programming knowledge (Matlab, Uniscript or similar)

KI-Beschreibung

As an OES Aftermarket Account Manager, you will focus on understanding customer needs and driving sales growth through effective quotations, marketing support, and strategic collaboration. This role involves tracking performance and ensuring customer satisfaction while maximizing sales and margins.

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  Bachelor's degree in business, marketing, or related field
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  Proven track record of success in sales leadership roles
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  Proficiency in CRM software and other sales tools

KI-Beschreibung

In this role, you will be involved in preparing and administering test vehicles, supporting software validation, and executing various system tests. Daily tasks will include hands-on activities such as installing equipment and managing software updates.

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  EU driving license B
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  Valid university enrollment certificate
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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