KI-Beschreibung

In this role, you will engage in method development and optimization while collaborating with cross-functional teams. Your expertise will drive the implementation of analytical methods and contribute to innovative solutions in pharmaceutical development.

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  University degree in pharmaceutical technology, biotechnology, biochemistry, chemistry, chemical engineering, or relevant natural science discipline
• •
  At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
• •
  Expertise in Biologics DS and DP process development applying QbD principles

Deine Vorteile

KI-Beschreibung

In this role, you will engage in method development and optimization for pharmaceutical drug processes, collaborating with teams to ensure compliance and efficiency. Your work will blend laboratory experiments with documentation, making a significant impact on healthcare innovation.

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  University degree in pharmaceutical technology, biotechnology, biochemistry, chemistry, chemical engineering, or relevant natural science discipline
• •
  At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
• •
  Expertise in Biologics DS and DP process development applying QbD principles

Deine Vorteile

KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies for drug development, ensuring compliance while driving innovation. Your role involves leading submission activities, managing documentation, and engaging with Health Authorities to navigate the regulatory landscape.

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  Minimum 5 years of regulatory CMC experience or pharmaceutical industry experience
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  Science degree or equivalent
• •
  Knowledge in regulatory submission and approval processes

Deine Vorteile

KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies and oversee submission activities, ensuring compliance while collaborating with cross-functional teams. This role involves proactive communication of risks and leading interactions with Health Authorities.

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  Minimum 5 years of regulatory CMC experience or pharmaceutical industry experience
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  Knowledge/
  experience in regulatory submission and approval processes
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  Ability to critically evaluate data from scientific disciplines

Deine Vorteile

KI-Beschreibung

In this role, you will oversee critical project tasks while authoring essential documentation. Your work will involve managing stability studies, validating methods, and ensuring compliance, all within a dynamic lab environment.

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  Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry, or similar
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  At least 4 years relevant industry experience or PhD in relevant field or equivalent
• •
  2+ years of work experience within the pharmaceutical industry

Deine Vorteile

KI-Beschreibung

In this role, you will oversee critical project tasks while authoring essential documentation. Your work will involve managing stability studies, validating methods, and ensuring compliance, all within a dynamic lab environment.

• •
  Master’s degree in biotechnology, biochemical engineering, biology, chemistry, biochemistry, or similar
• •
  At least 4 years relevant industry experience or PhD in relevant field or equivalent
• •
  2+ years of work experience within the pharmaceutical industry

Deine Vorteile

KI-Beschreibung

In this role, you will lead analytical projects and establish strategies for drug substance and product development. Your expertise will drive collaboration with teams and partners, ensuring efficient progress and compliance throughout the project lifecycle.

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  University degree in pharmaceutical technology, biotechnology, biochemistry, chemistry, chemical engineering, or relevant natural science discipline
• •
  At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
• •
  Expertise in Biologics DS and DP process development applying QbD principles

KI-Beschreibung

In this role, you will lead E&L project activities, conduct studies using advanced analytical techniques, and collaborate with various stakeholders. Your expertise will help adapt workflows and ensure compliance with evolving regulations in drug development.

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  University degree (preferably PhD) in Pharmacy, Polymer or Food Chemistry, Life Sciences or relevant science discipline
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  8+ years of working experience in pharma/
  biopharmaceutical industry or relevant industry
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  Expertise in analytical technologies: Headspace-GC/
  MS, LI-GC/
  (HR)MS, HPLC/
  (HR)MS, and related sample preparation techniques

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
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  Continued learning, dealing with ambiguity, GMP procedures, QA, QC testing, quality standards, self-awareness, technological expertise, technological intelligence

Deine Vorteile

KI-Beschreibung

In this role, you will lead E&L project activities, conduct studies using advanced analytical techniques, and collaborate with various stakeholders. Your expertise will help shape testing strategies and ensure compliance with evolving regulations.

• •
  University degree (preferably PhD) in Pharmacy, Polymer or Food Chemistry, Life Sciences or relevant science discipline
• •
  8+ years of working experience in pharma/
  biopharmaceutical industry or relevant industry
• •
  Expertise in analytical technologies: Headspace-GC/
  MS, LI-GC/
  (HR)MS, HPLC/
  (HR)MS, and related sample preparation techniques

Deine Vorteile

KI-Beschreibung

In this role, you will actively drive lab automation and digitalization efforts while planning and executing cell culture experiments. You will also mentor junior associates and ensure compliance with quality guidelines, contributing to the advancement of Biologics.

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  University degree (MSc, BSc) in life sciences, engineering, or equivalent
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  Minimum 6 years of experience in a related field
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  Strong practical experience in a laboratory and/
  or pilot plant environment

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing and validating cutting-edge container closure integrity testing methods, ensuring the quality of pharmaceutical products. Your work will involve collaboration with experts, troubleshooting challenges, and mentoring students, all while contributing to innovative solutions in a dynamic environment.

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  Bachelor’s, Master or PhD degree in engineering or natural sciences
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  Strong knowledge of container closure integrity testing and sterile drug products filling
• •
  Strong skills in cross-functional coordination and project management

Deine Vorteile

KI-Beschreibung

As a Senior Expert in Upstream Process Development, you will lead the characterization and transfer of cell culture processes, ensuring robust production for biotherapeutics. You will also mentor junior associates and contribute to innovative strategies.

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  University degree in life sciences, PhD with min. 2 years or Master with min. 6 years industrial experience or equivalent
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  Proven experience in upstream process transfer and collaboration with CMOs
• •
  Profound knowledge and hands-on experience in bioprocess engineering principles and upstream unit operations

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development of upstream cell culture processes while leveraging advanced modeling and AI tools. This position involves collaborating across teams to optimize production processes and mentoring junior scientists, all aimed at delivering innovative medicines to patients.

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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 or MSc with 6+ years of relevant experience
• •
  Hands-on experience in wet-lab bioprocess development and in-silico modeling approaches

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
• •
  Profound knowledge and hands-on experience in bioprocess engineering principles and upstream unit operations

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 enhance production processes and deliver innovative medicines to patients globally.

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  PhD in Biotechnology, (Bio)chemical Engineering or related field with 2+ years of experience in bioprocess development, modeling and digitalization, or MSc with 6+ years of relevant experience
• •
  Strong foundation in bioprocessing principles and upstream cell culture operations
• •
  Hands-on experience in wet-lab bioprocess development and in-silico modeling approaches

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 be at the forefront of developing and validating cutting-edge container closure integrity testing methods, ensuring the quality of pharmaceutical products. Your work will involve collaboration with experts, troubleshooting challenges, and mentoring students, all while contributing to innovative solutions in a dynamic environment.

• •
  Bachelor’s, Master or PhD degree in engineering or natural sciences
• •
  Strong knowledge of container closure integrity testing and sterile drug products filling
• •
  Strong skills in cross-functional coordination, project management, leading and influencing in global matrix organization

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing and validating cutting-edge container closure integrity testing methods, ensuring the quality of pharmaceutical products. Your work will involve collaboration with experts, troubleshooting challenges, and mentoring students, all while contributing to innovative solutions in a dynamic environment.

• •
  Bachelor’s, Master or PhD degree in engineering or natural sciences
• •
  Strong knowledge of container closure integrity testing and sterile drug products filling
• •
  Strong skills in cross-functional coordination, project management, and leading in global matrix organization

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.

• •
  PhD in Biotechnology, (Bio)chemical Engineering or related field
• •
  2+ years of experience in bioprocess development, modeling and digitalization or MSc with 6+ years of relevant experience
• •
  Hands-on experience in wet-lab bioprocess development and in-silico modeling approaches

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Technical Steward bist du verantwortlich für Technologie-Transfers und die kontinuierliche Verbesserung der pharmazeutischen Herstellungsprozesse. Du arbeitest eng mit verschiedenen Abteilungen zusammen, um sicherzustellen, dass die Produkte den höchsten Standards entsprechen.

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  Bachelor- oder Masterabschluss in Pharmazie, Chemie, Biotechnologie oder vergleichbar
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  Mehrjährige Erfahrung in pharmazeutischer Produktion, Technologie-Transfer oder MS&T
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  Fundierte Kenntnisse in cGMP, Validierung und regulatorischen Anforderungen

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Technical Steward bist du verantwortlich für Technologie-Transfers und die Optimierung pharmazeutischer Herstellungsprozesse. Du arbeitest eng mit verschiedenen Abteilungen zusammen, um sicherzustellen, dass die Produkte höchsten Standards entsprechen.

• •
  Bachelor- oder Masterabschluss in Pharmazie, Chemie, Biotechnologie oder vergleichbar
• •
  Mehrjährige Erfahrung in pharmazeutischer Produktion, Technologie-Transfer oder MS&T
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  Fundierte Kenntnisse in cGMP, Validierung und regulatorischen Anforderungen

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 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
• •
  Strong understanding of regulatory requirements and experience in preparing regulatory submissions

Deine Vorteile

KI-Beschreibung

In this role, you will provide scientific leadership in downstream processing, drive innovation, and ensure alignment with global drug substance 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
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  Proven track record in downstream process development
• •
  Strong understanding of regulatory requirements

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 skills in Python and C#

KI-Beschreibung

In dieser Schlüsselrolle sorgst du dafür, dass die Produktqualität und die Einhaltung regulatorischer Vorgaben in der pharmazeutischen Herstellung gewährleistet sind. Dein Alltag umfasst die Überwachung von GxP-Funktionen, die Leitung des Abweichungsmanagements und die Zusammenarbeit bei Audits, während du die Qualität lebensverändernder Medikamente sicherstellst.

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  Abgeschlossenes Hochschulstudium in Pharmazie, Biochemie, Biotechnologie, Chemie, Mikrobiologie oder abgeschlossene Berufsausbildung in einem relevanten pharmazeutischen Bereich
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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

Deine Vorteile

KI-Beschreibung

In this role, you will drive innovation and strategy in upstream process development, collaborating with global teams and leading initiatives that enhance scientific capabilities and ensure compliance in biotherapeutics manufacturing.

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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 MSc with 8+ years of relevant experience
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  Proven track record in late phase bioprocess development

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 sharing.

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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 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
• •
  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.

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

Deine Vorteile