KI-Beschreibung

As a Senior QA Compliance Specialist, you will engage in complaint investigations, ensuring quality and compliance while collaborating with various departments. This role also involves managing samples, identifying improvements, and maintaining up-to-date procedures for audits.

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  Degree in natural sciences (pharmacy, chemistry, medicine, biology, microbiology)
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  Experience in manufacturing medicinal products for human use
• •
  Working experience in GMP production, Quality Assurance, or Quality Control

Deine Vorteile

KI-Beschreibung

As a Senior QA Compliance Specialist, you will conduct complaint investigations to ensure quality and compliance while coordinating with various departments. This role also involves managing samples, identifying improvements, and keeping procedures up-to-date for audits.

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  Degree in natural sciences (pharmacy, chemistry, medicine, biology, microbiology)
• •
  Experience in manufacturing medicinal products for human use
• •
  Working experience in GMP production, Quality Assurance, or Quality Control

Deine Vorteile

KI-Beschreibung

In this role, you will focus on developing innovative syringe systems for radioligand therapies. You will collaborate with diverse teams to tackle design challenges and ensure compliance, while also driving the creation of essential technical documentation.

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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

In this role, you will engage in method development and optimization for pharmaceutical processes, collaborating with teams to ensure compliance 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
• •
  Advanced knowledge in Analytical Development

Deine Vorteile

KI-Beschreibung

In this role, you will oversee critical project tasks while authoring essential documentation. Your work will involve managing stability studies and validations, ensuring compliance, and supporting the lab team in resolving complex issues.

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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 lead analytical projects and develop strategies for drug substance and product processes. Your expertise will drive collaboration with teams and partners, ensuring efficient project management and innovative solutions in a dynamic environment.

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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
• •
  Advanced knowledge in Analytical Development

KI-Beschreibung

In this role, you will lead E&L project activities, conduct studies, and collaborate with various stakeholders. Your expertise will help adapt testing and assessment strategies, ensuring 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 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
• •
  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

As a Senior Expert in Science & Technology, you will lead upstream process development, transforming lab insights into scalable production processes while leveraging advanced modeling and AI tools to drive innovation in 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 6+ years of relevant experience with MSc
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  Strong foundation in bioprocessing principles and upstream cell culture operations

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, project management, and leading in global matrix organization

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
• •
  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 methods for container closure integrity testing, 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 influencing in global matrix organization

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development and transfer of upstream cell culture processes, collaborating with diverse teams to ensure robust production methods. Your expertise will help integrate innovative processes, mentor junior associates, and contribute to scientific advancements.

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  University degree in life sciences, PhD with min. 2 years or Master with min. 6 years industrial experience 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 process development, transforming lab insights into scalable production processes while leveraging advanced modeling and AI tools to drive innovation in biotherapeutics.

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  PhD in Biotechnology, (Bio)chemical Engineering or related field, or MSc with relevant experience
• •
  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

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 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
• •
  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 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 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 data science and automation projects, driving innovation in biopharmaceutical development. Your work will involve collaborating with teams, enhancing automation use cases, and ensuring alignment with business goals.

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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

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 for regulatory readiness, and driving 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

As a Drug Product Project Leader, you will drive the development of biologics, ensuring strategic alignment and timely delivery of high-quality documents while leading a global team 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 diverse team 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
• •
  Proficiency in quality principles, Quality by Design (QbD), Good Manufacturing Practice (GMP), and regulatory requirements

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, promoting 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

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, addressing quality issues, and collaborating on projects to enhance operational quality.

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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 addressing quality issues to enhance operational performance.

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  Quality assurance
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  Risk management
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  Agility

Deine Vorteile

KI-Beschreibung

In dieser Rolle bist du verantwortlich für die Weiterentwicklung des Qualitätsmanagementsystems und die Durchführung von Audits. Du sorgst für die kontinuierliche Verbesserung der Prozesse und koordinierst das Rohstoffmanagement, während du Schulungen durchführst und die Auswertung von Reklamationen übernimmst.

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  Abgeschlossenes Studium in Lebensmitteltechnologie, Ökotrophologie oder vergleichbar
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  Mehrjährige Berufserfahrung in lebensmittelproduzierenden Unternehmen, vorzugsweise im Bereich Qualitätsmanagement
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  Fundierte Kenntnisse im Bereich Lebenssicherheit und HACCP

Deine Vorteile