KI-Beschreibung

In this role, you will focus on managing regulatory submissions and ensuring compliance with standards. Your day-to-day responsibilities will involve collaborating with stakeholders and maintaining critical data in the Veeva Vault system.

• •
  Bachelor degree or proven related working experience in Life Sciences
• •
  Direct experience in regulatory affairs or critical areas in health industry
• •
  Working experience with regulatory information systems and platforms

Deine Vorteile

KI-Beschreibung

In this role, you will lead a team to enhance statistical programming efficiency, ensuring high-quality data analysis and compliance with regulatory standards while collaborating with various departments to meet project timelines.

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  15+ years experience in pharmaceutical industry, CRO, or clinical research setting with focus on oncology
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  Excellent knowledge of statistical programming in SAS including Base, macro, STAT, GRAPH, SQL
• •
  Bachelor’s degree in Statistics, Mathematics, Computer Science, or related discipline

KI-Beschreibung

As a Medical Director in Clinical Development, you will define and execute strategies for innovative Infectious Diseases programs, lead cross-functional teams, and drive clinical trial design to enhance patient outcomes in a fast-paced environment.

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  MD or MD-PhD with clinical background in infectious diseases
• •
  Multiple years of experience in vaccine or therapeutic development
• •
  Expertise in clinical trial strategy, design, and execution

Deine Vorteile

KI-Beschreibung

In this role, you will immerse yourself in a dynamic research environment, gaining hands-on experience in cutting-edge techniques while collaborating with top scientists and enhancing professional skills.

• •
  Bachelor or Master student

Deine Vorteile

KI-Beschreibung

As a Data Quality Expert, you will play a crucial role in promoting Ataccama ONE across business units, educating stakeholders on data quality initiatives, and translating technical requirements into actionable insights that drive business benefits.

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  Hands-on experience with Ataccama ONE
• •
  Strong technical understanding of data architecture
• •
  Experience implementing KPI monitoring and data quality rules

Deine Vorteile

KI-Beschreibung

As a Clinical Safety Manager, you will play a crucial role in overseeing safety and pharmacovigilance during clinical trials, ensuring compliance with regulations while safeguarding patient safety and enhancing global health.

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  Minimum 3 years of clinical research and pharmacovigilance experience
• •
  Strong knowledge of GCP, GVP, and regulatory requirements
• •
  Advanced degree in life sciences, pharmacy, public health, or related field

Deine Vorteile

KI-Beschreibung

In this role, you will engage with donors by conducting eligibility exams and providing essential information about plasma donation, all while ensuring their safety during the donation process.

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  Approbation als Arzt/
  Ärztin
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  Verantwortungs- und Einsatzbereitschaft
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  Teamarbeit

Deine Vorteile

KI-Beschreibung

In this role, you will lead complex clinical trials, ensuring smooth operations by managing timelines and vendor relationships. Your daily responsibilities will include facilitating communication, resolving issues, and maintaining inspection readiness throughout the clinical program lifecycle.

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  Minimum 10 years of experience in pharmaceutical/
  biotech or related industry
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  Oncology experience
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  Bachelor’s degree in life sciences or related field

KI-Beschreibung

In this role, you will take charge of specific sub-processes within the Source-to-Pay framework, collaborating with global stakeholders to enhance efficiency and drive digital transformation while ensuring compliance and alignment with organizational goals.

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  10+ years of experience in procurement or related field within large-scale, multinational environment
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  Bachelor's or Master's Degree in Business, Finance, Supply Chain, or related field
• •
  Proven ability to lead and influence in a matrixed, global environment

Deine Vorteile

KI-Beschreibung

In this strategic leadership role, you will be the technical voice for RNA and antibody products, ensuring compliance and driving excellence throughout the product lifecycle, from development to post-launch support.

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  Advanced degree in Biotechnology, Biochemistry, Chemical Engineering, or related field
• •
  Extensive experience in late-stage product development, commercial manufacturing, and technical lifecycle management
• •
  Proven track record in CMC leadership, including technical transfer, regulatory submissions, and post-approval change management

Deine Vorteile

KI-Beschreibung

In this role, you will play a key part in enhancing DD&I's processes by assisting with internal initiatives, identifying efficiency improvements, and conducting data analysis. Your contributions will help shape training materials and develop tools for effective business intelligence communication.

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  Currently pursuing a degree in Business Administration, Computer Science, Industrial Engineering, or a related field
• •
  Strong analytical skills
• •
  Proficiency in Microsoft Office applications, particularly Excel and PowerPoint

Deine Vorteile

KI-Beschreibung

As a Capture & Level Artist, you will creatively shape the presentation of Anno 117: Pax Romana through high-quality footage and screenshots. This role involves translating briefs into stunning visuals and preparing assets for 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
• •
  Hands-on experience with video editing software (e.g., Adobe Premiere, After Effects, or similar)

Deine Vorteile

KI-Beschreibung

In this role, you will support researchers in adhering to data management guidelines while ensuring data quality and compliance. Your daily responsibilities will include managing the research data sharing platform and educating staff on best practices.

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  Master’s degree or equivalent qualification in bioinformatics, computational biology, biological science, computer science, or other fields
• •
  Experience in working with big data, data management, and data repositories
• •
  Excellent written and oral communication skills in English

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of safety data analysis, transforming complex datasets into actionable insights while enhancing the analytics platform. Your work will directly support regulatory submissions and improve safety assessments across the innovative product portfolio.

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  Master’s degree in life sciences, computational sciences, data sciences, or related fields
• •
  Multiple years of experience in pharmaceutical/
  biotech data analysis and the pharmaceutical industry
• •
  Strong knowledge of pharmacovigilance regulations (GCP, GVP) and FDA, EMA, and ICH guidelines

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of scientific writing, generating essential documents for novel therapies from discovery to marketing approval. Your expertise will guide teams, ensure compliance, and foster knowledge in writing practices and regulatory standards.

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

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)
• •
  Proven experience in regulated, quality-controlled environments
• •
  Skilled in preparing and assembling regulatory documents

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development and execution of biomarker strategies for oncology programs, ensuring alignment with clinical objectives while collaborating with cross-functional teams to drive R&D success.

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  Ph.D. or MD in Immunology, molecular biology, pathology, or related discipline
• •
  6 to 10+ years of oncology clinical development experience
• •
  Experience with innovative assay development and problem-solving

Deine Vorteile

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
• •
  9+ years of working experience in Regulatory Affairs
• •
  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
• •
  Over 5 years of proven experience leading cross-functional teams
• •
  Expert knowledge of pharmaceutical drug-development processes

KI-Beschreibung

In this role, you will focus on enhancing quality processes through digitalization, collaborating with various teams to optimize workflows and ensure compliance with data integrity standards. Your work will drive continuous improvement and automation across the organization.

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  Bachelor's degree in Engineering Informatics, Technology, or similar
• •
  3-5 years of practical experience in quality engineering within a GMP environment
• •
  Knowledge of SAP-QM and preferably in Signavio

Deine Vorteile

KI-Beschreibung

In this role, you will lead the creation of high-quality scientific documents while managing a dynamic team. Your day-to-day responsibilities will include writing, coordinating, and ensuring compliance with regulatory standards, all while fostering a collaborative environment that adds value to the organization.

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  >10 years hands-on experience in drug development in a therapeutically relevant field, preferably in oncology and/
  or immunology
• •
  >10 years hands-on experience as a scientific or medical writer in the pharmaceutical/
  biotech industry
• •
  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
• •
  5+ years in pharmaceutical development, process improvement, or compliance
• •
  Deep understanding of global GxP requirements and regulatory frameworks

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
• •
  Industry experience in CMC development/
  commercial
• •
  In-depth knowledge of analytical techniques with hands-on experience in assay development and validation

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

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
• •
  Ability to translate business needs into technical requirements
• •
  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

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
• •
  Definition of concepts for products

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
• •
  Several years of experience in Immuno-Oncology
• •
  Thorough understanding of clinical development methods

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 internship, you will explore various engineering fields, conducting market analyses for international projects and supporting design and simulation tasks. Your contributions will help shape innovative solutions across multiple disciplines.