KI-Beschreibung

As a Quality Team Leader QC, you will guide a dedicated team to uphold the highest quality standards in testing and compliance. This role involves overseeing operations, supporting audits, and driving continuous improvement to ensure safe, high-quality medicines reach patients worldwide.

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  Minimum 5 years of experience in Quality Control, Quality Assurance, or Production within the pharmaceutical industry
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  Strong understanding of cGxP principles, analytical methods, and regulatory requirements
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  Proven leadership experience in managing laboratory teams and operations

Deine Vorteile

KI-Beschreibung

In this role, you will focus on developing innovative parenteral packaging solutions for radioligand therapies. You will collaborate with diverse teams to create effective syringe systems while ensuring compliance and functionality throughout the process.

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  Master’s or PhD in engineering, materials science, pharmaceutical technology, or related discipline
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  Minimum of 3 years’ experience in a comparable position, ideally within primary packaging, medical device, combination product development, or pharmaceutical industries
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  Demonstrated ability to lead and influence within a global, matrixed organization

Deine Vorteile

KI-Beschreibung

As a Senior Expert in Parenteral Packaging Technology, you will focus on developing innovative syringe systems for radioligand therapies, collaborating with diverse teams to ensure effective packaging solutions and compliance with regulatory standards.

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  Master’s or PhD in engineering, materials science, pharmaceutical technology, or related discipline
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  Minimum of 3 years’ experience in a comparable position, ideally within primary packaging, medical device, combination product development, or pharmaceutical industries
• •
  Demonstrated ability to lead and influence within a global, matrixed organization

Deine Vorteile

KI-Beschreibung

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

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  University degree in pharmaceutical technology, biotechnology, biochemistry, chemistry, chemical engineering, or relevant natural science discipline
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  At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
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  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 processes, collaborating with teams to ensure quality and efficiency. Your work will blend laboratory experiments with documentation, making a significant impact on healthcare advancements.

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  At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
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  Expertise in Biologics DS and DP process development applying QbD principles
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  Advanced knowledge in Analytical Development

Deine Vorteile

KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies and oversee submission activities, ensuring compliance and quality. This role involves proactive communication with stakeholders and leading interactions with Health Authorities to drive successful outcomes.

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

Deine Vorteile

KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies and oversee submission activities, ensuring compliance and quality. This role involves proactive communication with teams and leading interactions with Health Authorities to support product development.

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

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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
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  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
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  At least 3 years (PhD) or 6 years (MSc) of working experience in the (bio)pharmaceutical industry
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  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 shape testing strategies and ensure compliance with evolving regulations.

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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 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
• •
  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 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 be at the forefront of developing and validating cutting-edge testing methods for container closure integrity, 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
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  Strong skills in cross-functional coordination and project management

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.

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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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  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
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  Strong foundation in bioprocessing principles and upstream cell culture operations
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  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.

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  University degree in life sciences, biotechnology, bioprocess engineering, or equivalent
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  PhD with minimum 2 years or Master with minimum 6 years industrial experience or equivalent
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  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.

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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
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  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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  Abgeschlossenes Studium in Pharmazie, Chemie, Biotechnologie oder vergleichbar
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  Mehrjährige Erfahrung in der pharmazeutischen 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.

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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 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 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
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  Strong understanding of regulatory requirements

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
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  6+ years of experience in USP process development
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  Proven track record in late phase bioprocess development

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
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  Proven track record in late phase bioprocess development

Deine Vorteile

KI-Beschreibung

In dieser Schlüsselrolle sorgst du dafür, dass die pharmazeutische Produktion höchsten Qualitäts- und Compliance-Standards entspricht. Dein Alltag umfasst die Überwachung von GxP-Funktionen, die Leitung des Abweichungsmanagements und die Zusammenarbeit bei Audits, um die Sicherheit der Patienten und die Exzellenz der Produkte zu gewährleisten.

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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 lead data science and automation projects, driving innovation in biopharmaceutical development. Your work will involve collaboration with teams, enhancing digital initiatives, and conducting scientific experiments to support process characterization.

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

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 role, you will tackle complex biopharmaceutical challenges by developing robust models that guide 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