KI-Beschreibung

In this role, you will lead upstream cell culture process development, utilizing expertise in bioprocess modeling and AI to transform data into actionable insights. The position involves collaboration across teams, mentoring junior associates, and contributing to innovative scientific advancements.

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  PhD in Biotechnology, (Bio)chemical Engineering, or related field
• •
  2+ years of experience in bioprocess development, modeling, and digitalization
• •
  Strong foundation in bioprocessing principles

Deine Vorteile

KI-Beschreibung

As a Senior Expert in Science & Technology, you will lead upstream cell culture process development, utilizing expertise in bioprocess modeling and AI to drive innovation and optimize production processes for biotherapeutics.

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  PhD in Biotechnology, (Bio)chemical Engineering, or related field
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  2+ years of experience in bioprocess development, modeling, and digitalization
• •
  Strong foundation in bioprocessing principles

Deine Vorteile

KI-Beschreibung

In this role, you will focus on developing and implementing automation solutions in analytical labs while collaborating with local and international teams. Your daily responsibilities will include managing projects, ensuring compliance with quality standards, and driving innovation in lab automation.

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  Automation experience
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  Minimum 5 years of experience
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  Coding in Python and C#

KI-Beschreibung

In this role, you will provide scientific leadership in downstream processing, drive innovation, and ensure alignment with global drug substance development strategies. Your day-to-day responsibilities will involve leading projects, coaching experts, and integrating advanced technologies into development workflows.

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  Ph.D. in biotechnology, biochemical engineering, biochemistry, molecular biology, biology, chemistry, chemical engineering, or related field with 6+ years of relevant experience or Master's degree with 8+ years of relevant experience
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  Proven track record of leading downstream process development in pharmaceutical or biotechnology industry
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  Strong understanding of regulatory requirements and experience in preparing regulatory submissions

Deine Vorteile

KI-Beschreibung

In this role, you will lead the strategic vision for upstream process development, driving innovation and collaboration across global networks. Your expertise will guide scientists and support complex projects, ensuring compliance and advancing scientific capabilities.

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  PhD in Biotechnology, Biochemical or Bioprocess Engineering, or related field
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  6+ years of experience in USP process development or 8+ years of relevant experience with MSc
• •
  Proven track record in late phase bioprocess development

Deine Vorteile

KI-Beschreibung

In this role, you will provide scientific leadership in downstream processing, drive innovation, and ensure alignment with global drug substance development strategies. Your day-to-day responsibilities will involve leading projects, coaching experts, and overseeing major transformations while collaborating across teams.

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  Ph.D. in biotechnology, biochemical engineering, biochemistry, molecular biology, biology, chemistry, chemical engineering, or related field with 6+ years of relevant experience or Master's degree with 8+ years of relevant experience
• •
  Proven track record of leading downstream process development in pharmaceutical or biotechnology industry
• •
  Strong understanding of regulatory requirements and experience in preparing regulatory submissions

Deine Vorteile

KI-Beschreibung

In dieser Schlüsselrolle sorgst du dafür, dass die Produktqualität und die regulatorischen Vorgaben in der pharmazeutischen Herstellung eingehalten werden. Du überwachst GxP-Funktionen, leitest das Beschwerdemanagement und bist der zentrale Ansprechpartner für SAP- und GLIMS-Aktivitäten.

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  Berufserfahrung in der pharmazeutischen Industrie, idealerweise mindestens 2 Jahre im Bereich Qualitätssicherung
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  Fundierte Kenntnisse der aktuellen Good Manufacturing Practices (cGMP) und regulatorischer Anforderungen
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  Nachweisbare Erfahrung im Umgang mit Behörden wie FDA, EMA oder anderen Gesundheitsbehörden

Deine Vorteile

KI-Beschreibung

In this role, you will lead strategic initiatives in upstream process development, drive innovation, and support complex projects while ensuring compliance with regulatory standards. Your expertise will shape the future of biotherapeutics through collaboration and knowledge exchange.

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  PhD in Biotechnology, Biochemical or Bioprocess Engineering, or related field
• •
  6+ years of experience in USP process development
• •
  Proven track record in late phase bioprocess development

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development and transfer of upstream cell culture processes, collaborating with cross-functional teams to ensure robust production methods. Your expertise will help integrate innovative processes and mentor junior associates, while contributing to life-changing medicines for patients worldwide.

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  University degree in life sciences, biotechnology, bioprocess engineering, or equivalent
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  Proven experience in upstream process transfer and collaboration with CMOs
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  Experience with statistical methods (DoE, MVDA) and data-driven or mechanistic models

Deine Vorteile

KI-Beschreibung

In this role, you will lead the scientific strategy for Biologic Drug Product development, collaborating closely with project managers and teams. Your day-to-day responsibilities will include designing experiments, managing technology transfers, and presenting findings, all while ensuring regulatory compliance and technical excellence.

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  Experience of 2-5 years in biotech or pharmaceutical industry with focus on formulation or manufacturing processes development, technical transfer, validation, and submission
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  PhD or Master in pharmaceutical technology, biotechnology, chemical engineering, or relevant discipline
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  Solid understanding of quality standards and regulations in pharmaceutical industry

Deine Vorteile

KI-Beschreibung

In this role, you will lead the scientific strategy for Biologic Drug Product development, collaborating closely with project managers and teams. Your day-to-day responsibilities will include designing experiments, managing technology transfers, and presenting findings, all while ensuring regulatory compliance and technical excellence.

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  2-5 years of experience in biotech/
  pharmaceutical industry with focus on formulation or manufacturing processes development, technical transfer, validation, and submission
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  PhD or Master in pharmaceutical technology, biotechnology, chemical engineering, or relevant discipline
• •
  Solid understanding of quality standards and regulations in pharmaceutical industry

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development and transfer of upstream cell culture processes, ensuring robust production for biotherapeutics. Your expertise will drive innovation and collaboration across teams, while mentoring junior associates and contributing to scientific advancements.

• •
  University degree in life sciences, biotechnology, bioprocess engineering, or equivalent
• •
  Proven experience in upstream process transfer and collaboration with CMOs
• •
  Experience with statistical methods (DoE, MVDA) and data-driven or mechanistic models

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development and transfer of upstream cell culture processes, ensuring robust production for biotherapeutics. Your expertise will drive innovation and collaboration across teams, while mentoring junior associates and contributing to scientific advancements.

• •
  University degree in life sciences, biotechnology, bioprocess engineering, or equivalent
• •
  PhD with minimum 2 years or Master with minimum 6 years industrial experience or equivalent
• •
  Proven experience in upstream process transfer and collaboration with CMOs

Deine Vorteile

KI-Beschreibung

In this role, you will lead the scientific strategy for Biologic Drug Product development, collaborating closely with project managers and teams. Your day-to-day responsibilities will include designing experiments, managing technology transfers, and presenting findings, all while ensuring regulatory compliance and driving innovative solutions.

• •
  PhD or Master in pharmaceutical technology, biotechnology, chemical engineering, or relevant discipline
• •
  Experience of 2-5 years in biotech or pharmaceutical industry with focus on formulation or manufacturing processes development, technical transfer, validation, and submission
• •
  Solid understanding of quality standards and regulations in pharmaceutical industry

Deine Vorteile

KI-Beschreibung

In this role, you will lead data science and automation projects, driving innovation in biopharmaceutical development. Your expertise will shape strategies, enhance digital initiatives, and ensure alignment with business goals.

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  Experience in data science, data engineering, and automation
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  Proficiency in programming languages such as Python, R, or SQL
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  Strong expertise in designing and optimizing data flows

KI-Beschreibung

As a Drug Substance Project Lead, you will coordinate a dedicated team and oversee all aspects of drug substance development, including process validation and budget management, while ensuring effective communication across various organizational levels.

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  Minimum of 5 years relevant experience in Biologics CMC development or production
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  MSc or PhD in Natural Science
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  Proficiency in English

Deine Vorteile

KI-Beschreibung

In this role, you will tackle complex biopharmaceutical challenges by developing robust models that inform experimental design and process optimization. Your work will involve collaboration with cross-functional teams, ensuring data quality, mentoring others, and contributing to regulatory submissions and continuous improvement initiatives.

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  Master’s or PhD in Chemical Engineering, Biochemical Engineering, Bioprocess Technology, Bioinformatics, or related fields
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  Strong foundation in process modeling
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  Proficiency in R or Python

KI-Beschreibung

In this role, you will leverage your expertise in downstream process development to create robust models that address complex biopharmaceutical challenges. Your work will involve collaborating with cross-functional teams, ensuring model credibility, and preparing scientific documents for regulatory submissions.

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  Master’s or PhD in Chemical Engineering, Biochemical Engineering, Bioprocess Technology, Bioinformatics, or related fields
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  Strong foundation in process modeling
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  Proficiency in R or Python

KI-Beschreibung

In this role, you will lead downstream process development for biopharmaceutical projects, conduct experiments, and ensure compliance with quality standards. Your expertise will drive innovation while collaborating with internal teams and external partners.

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  Completed studies in Biotechnology, Process Engineering, Biology, Biochemistry, Pharmaceutical Technology, Technical Chemistry, Pharmacy
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  Experience in Downstream Processing, particularly with chromatography systems, e.g. ÄKTA systems
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  Proficiency in programming languages such as Python, R, or SQL

KI-Beschreibung

In this part-time role, you will focus on ensuring product quality and compliance with GxP standards. Daily tasks will involve managing quality systems, supporting product releases, and collaborating on audits, all while maintaining a commitment to safety and regulatory adherence.

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  Microbiology or finalized apprenticeship in Pharmaceutical industry or equivalent
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  Fluency in German and intermediate proficiency in English
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  GMP procedures

Deine Vorteile

KI-Beschreibung

In this part-time role, you will play a crucial part in maintaining product quality and ensuring compliance with GxP standards. Daily tasks will involve overseeing quality systems, managing deviations, and supporting product release and validation projects.

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  Microbiology or finalized apprenticeship in the Pharmaceutical industry, or equivalent
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  Fluency in German and intermediate proficiency in English

Deine Vorteile

KI-Beschreibung

As a Drug Product Project Leader, you will drive the late-stage development of biologics, ensuring strategic alignment and timely delivery of high-quality documentation while leading a global team of experts and engaging with key stakeholders.

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  Ph.D. in pharmaceutical technology, biotechnology, chemical engineering, or equivalent
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  Minimum of 8 years of relevant industry experience
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  Proficiency in quality principles, Quality by Design (QbD), Good Manufacturing Practice (GMP), and regulatory requirements

Deine Vorteile

KI-Beschreibung

As a Drug Product Project Leader, you will drive the late-stage development of biologics, ensuring strategic alignment and timely delivery of high-quality documentation while leading a global team of experts and engaging with key stakeholders.

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  Ph.D. in pharmaceutical technology, biotechnology, chemical engineering, or equivalent
• •
  Minimum of 8 years of relevant industry experience
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  Proficiency in quality principles, QbD, GMP, and regulatory requirements

Deine Vorteile

KI-Beschreibung

As a QA Operations Team Leader, you will guide a team of Qualified Persons to ensure the compliant release of pharmaceutical products. This role involves managing resources, resolving quality issues, and fostering a culture of continuous improvement.

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  Minimum 7 years of experience in Quality Assurance
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  Qualified Person (QP) as per EU Directive 2001/
  83/
  EC
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  Minimum 4 years of experience as a certified Qualified Person (QP)

Deine Vorteile

KI-Beschreibung

In this role, you will lead a team of Qualified Persons to ensure the compliant release of pharmaceutical products. Your daily responsibilities will include mentoring the team, managing workloads, and collaborating with various departments to resolve quality issues.

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  Minimum 7 years of experience in Quality Assurance within the pharmaceutical industry
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  Qualified Person (QP) as per EU Directive 2001/
  83/
  EC
• •
  Extensive knowledge of EU GMP regulations and relevant national legislation

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing user-friendly drug delivery devices. Your daily work will involve conducting research, collaborating with diverse teams, and ensuring that products meet regulatory standards while prioritizing the end-user experience.

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  MSc in Human Factors Engineering, Cognitive Sciences, Behavioral Sciences, Biomedical Engineering, Psychology, Product Design, or Mechanical Engineering
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  3+ years of experience in human factors engineering, preferably in medical devices or combination products
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  Strong understanding of usability engineering standards (e.g., IEC 62366, ISO 14971)

KI-Beschreibung

In this role, you will oversee the integration of new technologies in quality assurance, manage complex global projects, and ensure compliance with GMP standards. Your work will involve collaborating with various teams to drive digitalization and enhance quality processes within TRD.

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  5+ years of relevant experience in development quality environment
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  Experience in project management or operations management
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  Strong quality background

Deine Vorteile

KI-Beschreibung

In this role, you will oversee the integration of new technologies in TRD and drive digitalization strategies. Your day-to-day responsibilities will include managing QA oversight for projects, fostering AI usage, and ensuring compliance with GMP standards while collaborating with various teams.

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  5+ years of relevant experience in development quality environment
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  Experience in project management or operations management
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  Strong quality background and innovation in Data & Digital

Deine Vorteile

KI-Beschreibung

As an R&D Senior Quality Manager, you will play a crucial role in ensuring compliance with regulatory standards while managing quality initiatives. Your day-to-day responsibilities will involve supporting inspections, developing quality plans, and driving improvements in operational quality and compliance.

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  Project management skills
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  Critical negotiation skills
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  Agility, analytical development

Deine Vorteile

KI-Beschreibung

As an R&D Senior Quality Manager, you will play a crucial role in ensuring compliance with regulatory standards while supporting quality initiatives. Your day-to-day responsibilities will include managing quality plans, conducting audits, and collaborating on projects to enhance operational quality.

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  Quality assurance knowledge
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  Risk management
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  Project management

Deine Vorteile