KI-Beschreibung

In this role, you will lead E&L project activities, conduct studies on various materials, and collaborate with internal and external partners. 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 be at the forefront of developing innovative combination products, ensuring that device components meet high-quality standards for both clinical trials and commercial production while navigating regulatory requirements.

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  Bachelor, Master, or PhD degree in engineering or equivalent
• •
  Preferably 5+ years of experience in development of medical devices or combination products
• •
  Experience in developing plastic and metal components, tolerance analysis, modelling, and testing

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 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.

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  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

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 and project management

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing innovative parenteral combination products, collaborating with cross-functional teams to ensure safety, usability, and compliance throughout the product life cycle.

• •
  5+ years of experience in development of medical devices or combination products
• •
  Bachelor, Master or PhD degree in engineering or equivalent
• •
  Experience in developing plastic and metal components, tolerance analysis, modelling and testing

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
• •
  Minimum 6 years of experience in a related field
• •
  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.

• •
  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 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.

• •
  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

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
• •
  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

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
• •
  MSc or PhD in Natural Science
• •
  Proficiency in English

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 and safety standards, and driving innovation in lab automation.

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  Automation experience
• •
  Minimum 5 years of experience
• •
  Coding skills 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.

• •
  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 be at the forefront of developing analytical data packages for drug-device combination products, coordinating tasks across teams, and ensuring compliance with regulatory standards. Your expertise will guide project resources, manage external partnerships, and mentor team members, making a significant impact on product development.

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  Master or PhD in engineering, chemical/
  bio analytics, or equivalent
• •
  Significant working experience in pharmaceutical industry in combination product development
• •
  Proven knowledge in late phase parenteral analytical 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 strategies. Your day-to-day responsibilities will include leading projects, coaching experts, and overseeing critical transformations in late-phase development.

• •
  Ph.D. in biotechnology, biochemical engineering, biochemistry, molecular biology, biology, chemistry, chemical engineering, or related field with 6+ years of relevant experience
• •
  Master's degree with 8+ years of relevant experience
• •
  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
• •
  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 shape the strategic vision for upstream process development, drive innovation, and collaborate with global teams. Your expertise will guide scientists and support complex projects, ensuring compliance and advancing scientific capabilities.

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

Deine Vorteile

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
• •
  Berufserfahrung in der pharmazeutischen Industrie, idealerweise mindestens 2 Jahre im Bereich Qualitätssicherung
• •
  Fundierte Kenntnisse der aktuellen Good Manufacturing Practices (cGMP) und regulatorischer Anforderungen

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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  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 the scientific strategy for Biologic Drug Product development, collaborating with project managers and scientists. Your daily responsibilities will include designing technical activities, managing technology transfers, and presenting findings to diverse audiences.

• •
  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 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 or pharmaceutical industry with focus on formulation or manufacturing processes development, technical transfer, validation, and submission
• •
  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 data science and automation projects, driving innovation in biopharmaceutical development. Your day-to-day responsibilities will involve collaborating with teams, enhancing automation strategies, and generating critical experimental data.

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

KI-Beschreibung

In this role, you will lead a team focused on identifying and mitigating risks in drug-device combination products. You will ensure that quality control strategies align with regulatory standards while fostering a high-performing and diverse team culture.

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  Master or PhD in engineering, pharmaceutical field, or equivalent
• •
  Extensive working experience in pharmaceutical industry
• •
  Proven knowledge in risk management and control strategy

Deine Vorteile

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 and support regulatory submissions while collaborating with internal and external partners.

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

KI-Beschreibung

In this role, you will leverage your expertise to transform complex biopharmaceutical challenges into effective models, guiding experimental design and optimizing processes. Collaborating with cross-functional teams will ensure that modeling is seamlessly integrated into development workflows, while you also mentor others and contribute to scientific advancements.

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  Master’s or PhD in Chemical Engineering, Biochemical Engineering, Bioprocess Technology, Bioinformatics, or related fields
• •
  Strong foundation in process modeling
• •
  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.

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

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
• •
  Fluency in German and intermediate proficiency in English
• •
  GMP procedures

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.

• •
  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

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.

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

• •
  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