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

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.

• •
  Bachelor, Master, or PhD degree in engineering or equivalent
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  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 QA Compliance Specialist, you will dive into complaint investigations, ensuring quality and compliance while coordinating with various departments. This role also involves managing samples, identifying improvements, and supporting audits to maintain high standards.

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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
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  Working experience in GMP production, Quality Assurance, or Quality Control

Deine Vorteile

KI-Beschreibung

As a Senior QA Compliance Specialist, you will dive into complaint investigations, ensuring quality and compliance while coordinating with various departments. This role also involves managing samples, identifying improvements, and preparing for audits, all while maintaining high health and safety standards.

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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
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  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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  Experience with radioligand therapies (RLT) is a significant plus

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
• •
  Experience with radioligand therapies (RLT) is a significant plus

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

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
• •
  Expertise in Biologics DS and DP process development applying QbD principles

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 troubleshooting 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
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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 develop strategies for drug substance and product processes. Your expertise will drive collaboration with teams and partners, ensuring efficient project execution and compliance with regulatory standards.

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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
• •
  Expertise in Biologics DS and DP process development applying QbD principles

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 execution and compliance with regulatory standards.

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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 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 influencing in global matrix organization

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.

• •
  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 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.

• •
  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

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
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  Strong foundation in bioprocessing principles

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
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  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 or 6+ years of relevant experience with MSc
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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 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 development strategies. Your day-to-day responsibilities will involve leading key projects, coaching experts, and overseeing major transformations while collaborating across teams to integrate development and manufacturing strategies.

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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 strategic initiatives in upstream process development, drive scientific innovation, and support complex projects while ensuring compliance with regulatory standards. Your expertise will shape the future of 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
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  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 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 data science and automation projects, driving innovation in biopharmaceutical development. Your expertise will help shape strategies, enhance digital initiatives, and ensure alignment with business goals while collaborating with cross-functional teams.

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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

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 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 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

In dieser Rolle als Senior Embedded Software Engineer entwickelst du Firmware für moderne ARM-Plattformen und integrierst Kommunikations-Stacks für industrielle Anwendungen. Du arbeitest eng mit dem Hardware-Team zusammen und sorgst für hohe Code-Qualität, während du jüngere Entwickler:innen unterstützt und an wichtigen Architekturentscheidungen mitwirkst.

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  Mindestens 6–7 Jahre Erfahrung in Embedded-Entwicklung mit C
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  Erfahrung mit RTOS oder Bare-Metal, gute Linux-Grundlagen
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  Fundierte Kenntnisse in Kommunikationsprotokollen (CAN/
  CAN FD, Ethernet, PROFINET) und Bus-/
  Frame-Analyse

Deine Vorteile

KI-Beschreibung

Als Go Developer:in arbeitest du an der Entwicklung einer innovativen IoT- und Kommunikationsplattform. Dein Alltag umfasst die Backend- und Frontend-Entwicklung, die Sicherstellung der Code-Qualität sowie die enge Zusammenarbeit mit dem Product Owner und dem Entwicklerteam.

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  Mindestens 5 Jahre Erfahrung in Full-Stack-Entwicklung
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  Sehr gute Kenntnisse in Go, HTMX und Templ oder vergleichbaren Go-Template-Engines
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  Fundierte Datenbankkenntnisse (PostgreSQL)

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Senior Golang Software Entwickler:in bist du für die gesamte Entwicklung von IoT- und Kommunikationsanwendungen verantwortlich. Du arbeitest an der Backend- und Frontend-Entwicklung, optimierst Datenbanken und sorgst für hohe Code-Qualität, während du eng mit dem Product Owner und dem Team zusammenarbeitest.

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  Mindestens 5 Jahre Erfahrung in Full-Stack-Entwicklung
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  Sehr gute Kenntnisse in Go, HTMX und Templ oder vergleichbaren Go-Template-Engines
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  Fundierte Datenbankkenntnisse (PostgreSQL)

Deine Vorteile

KI-Beschreibung

Als IIoT Sales Manager bist du der Treiber für innovative industrielle Kommunikation in der DACH-Region. Du baust Neukunden auf, entwickelst Key Accounts weiter und positionierst Spitzentechnologien bei Entscheidern, während du gleichzeitig die Pipeline sorgfältig pflegst.

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  Mindestens 5 Jahre B2B-Vertriebserfahrung im Industrie-, Automations- oder IIoT-Umfeld
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  Nachweisbare Erfahrung im Aufbau von Neukunden und im Schließen komplexer Deals
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  Erfahrung in Enterprise-Sales

Deine Vorteile