KI-Beschreibung

As a QA Operations Expert, you will play a crucial role in maintaining high-quality standards across operations. Your daily tasks will involve overseeing compliance, managing batch releases, and supporting continuous improvement initiatives.

• •
  University Degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology, or equivalent
• •
  Professional experience in Pharmaceutical industry, Biopharmaceutical or API products and at least 2 years within QA
• •
  Accountability and reliability

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
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  Preferably 5+ years of experience in development of medical devices or combination products
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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.

• •
  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

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)
• •
  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 become a key player in primary packaging development, focusing on selecting and assessing packaging solutions while ensuring compliance and functionality. Your day-to-day responsibilities will involve collaborating with stakeholders, resolving technical issues, and preparing essential documentation for medical device registration.

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  Bachelor or master’s in engineering, materials science, pharmaceutical technology, or related discipline
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  Experience in primary packaging, medical device, combination product, or pharmaceutical
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  Strong communication skills and ability to connect across functions

Deine Vorteile

KI-Beschreibung

In this role, you will dive into the world of primary packaging, assess solutions, and ensure compliance while collaborating with stakeholders. Your day-to-day responsibilities will involve problem-solving and preparing essential documentation for medical device registration.

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  Bachelor or master’s in engineering, materials science, pharmaceutical technology, or related discipline
• •
  Experience in primary packaging, medical device, combination product, or pharmaceutical
• •
  Strong communication skills and ability to connect across functions

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
• •
  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
• •
  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 leverage your MES expertise to enhance pharmaceutical manufacturing processes, ensuring quality and efficiency. You will also train staff and collaborate on continuous improvements to deliver essential medications globally.

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  Experience in food, drug, or medical device regulated industry for at least 3 years
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  Background in IT, Engineering, Computer Science, or related field
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  Experience in an MES system

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 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
• •
  2+ years of work experience within the pharmaceutical industry

Deine Vorteile

KI-Beschreibung

In this role, you will actively drive lab automation and digitalization efforts while implementing new technologies. Your day-to-day responsibilities will involve planning experiments, mentoring team members, and ensuring compliance with quality standards.

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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
• •
  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 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 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 in life sciences, engineering, or equivalent
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  Minimum 2 years of relevant experience
• •
  Strong practical experience in a laboratory and/
  or pilot plant environment

Deine Vorteile

KI-Beschreibung

In this role, you will actively drive lab automation and digitalization efforts, plan and execute cell culture experiments, and mentor junior associates, all while ensuring compliance with quality standards in the development labs.

• •
  University degree (MSc, BSc) in life sciences, engineering, or equivalent
• •
  Minimum 2 years of relevant experience
• •
  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 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

In dieser Rolle bist du für die Wartung und Optimierung von Pharma-Anlagen verantwortlich. Du dokumentierst die Arbeit im SAP-System, bearbeitest Störmeldungen und unterstützt technische Teams bei Fehleranalysen, um die Anlagenverfügbarkeit zu gewährleisten.

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  Abgeschlossene Lehre als Metalltechniker, Mechaniker, Mechatroniker oder vergleichbar
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  Sehr gute Deutschkenntnisse und Englischkenntnisse von Vorteil
• •
  Genaues Arbeiten und Dokumentation

Deine Vorteile

KI-Beschreibung

In dieser Rolle bist du für die Wartung und Optimierung von Pharma-Anlagen verantwortlich. Du dokumentierst deine Arbeit im SAP-System und unterstützt das Team bei technischen Herausforderungen, um die Verfügbarkeit der Anlagen sicherzustellen.

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  Abgeschlossene Lehre als Metalltechniker, Mechaniker, Mechatroniker oder vergleichbar
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  Sehr gute Deutschkenntnisse, Englischkenntnisse von Vorteil
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  Genaues Arbeiten und Dokumentation, Teamplayer, Interesse am Bereitschaftsdienst, hohe Lernbereitschaft, Offenheit für neue Herausforderungen

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Technical Steward bist du verantwortlich für die Leitung von Technologie-Transfer-Projekten und die Sicherstellung eines kontinuierlich verbesserten Produktionsprozesses. Du arbeitest eng mit verschiedenen Schnittstellen zusammen und bringst deine Expertise ein, um die höchsten Standards in der pharmazeutischen Produktion zu gewährleisten.

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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 Prozessvalidierungen. Du arbeitest eng mit verschiedenen Abteilungen zusammen, um sicherzustellen, dass die Produktionsprozesse kontinuierlich verbessert werden und den höchsten Standards entsprechen.

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  Abgeschlossenes Studium in Pharmazie, Chemie, Biotechnologie oder vergleichbar
• •
  Mehrjährige Erfahrung in der pharmazeutischen Produktion, Technologie-Transfer oder MS&T
• •
  Fundierte Kenntnisse in cGMP, Validierung und regulatorischen Anforderungen

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 leverage your MES expertise to enhance pharmaceutical manufacturing processes, ensuring quality and efficiency. You will also train staff and collaborate on continuous improvements in a dynamic environment.

• •
  Experience in food, drug, or medical device regulated industry for at least 3 years
• •
  Experience in an MES system
• •
  Background in IT, Engineering, Computer Science, or related field

Deine Vorteile

KI-Beschreibung

As a Manufacturing Systems Expert, you will leverage your MES PAS-X expertise to enhance pharmaceutical manufacturing processes. Your role involves ensuring system efficiency, conducting training, and collaborating with engineers to drive continuous improvement in drug production.

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  Experience in food, drug, or medical device regulated industry for at least 3 years
• •
  Background in IT, Engineering, Computer Science, or related field
• •
  Experience in an MES system

Deine Vorteile

KI-Beschreibung

In dieser Rolle bist du Teil eines dynamischen Teams, das für die Wartung und Instandhaltung von 80 Anlagen verantwortlich ist. Du bereitest Materialien vor, überwachst Wartungsarbeiten und sorgst dafür, dass alles reibungslos läuft, um die Versorgung mit hochwertigen Arzneimitteln sicherzustellen.

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  Abgeschlossene Lehre in einem einschlägigen Fachbereich
• •
  Technisches Verständnis von korrektiver und präventiver Wartung
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  Problemlösung über Funktionsbereiche hinweg

Deine Vorteile

KI-Beschreibung

In dieser Rolle bist du für die Vorbereitung von Werkzeugen und Materialien sowie die Durchführung von Wartungsaufträgen verantwortlich. Du überwachst die Qualität der Arbeiten und dokumentierst alle Vorgänge sorgfältig, während du technische Beschwerden zeitnah meldest.

• •
  Abgeschlossene Lehre in einem einschlägigen Fachbereich
• •
  Technisches Verständnis von korrektiver und präventiver Wartung
• •
  Problemlösung über Funktionsbereiche hinweg

Deine Vorteile

KI-Beschreibung

As a QA Operations Expert, you will play a crucial role in ensuring that production and testing activities meet quality standards and regulatory compliance. Your day-to-day responsibilities will involve overseeing operations, managing batch releases, and supporting continuous improvement initiatives.

• •
  University degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology, or equivalent
• •
  Professional experience in Pharmaceutical industry, Biopharmaceutical or API products and at least 2 years within QA
• •
  KLL - Kontrollaborleiter(in) qualification

Deine Vorteile

KI-Beschreibung

As a QA Operations Expert, you will play a crucial role in ensuring that production and testing activities meet stringent quality standards. Daily tasks will involve overseeing compliance with regulations, managing batch releases, and supporting continuous improvement initiatives.

• •
  University Degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology, or equivalent
• •
  Professional experience in Pharmaceutical industry, Biopharmaceutical or API products and at least 2 years within QA
• •
  KLL - Kontrollaborleiter(in) qualification

Deine Vorteile

KI-Beschreibung

As a QA Operations Expert, you will ensure that production and testing activities meet quality standards and regulatory requirements. Your role involves overseeing compliance, managing batch releases, and supporting continuous improvement initiatives.

• •
  University degree in Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology, or equivalent
• •
  Professional experience in Pharmaceutical industry, Biopharmaceutical or API products and at least 2 years within QA
• •
  KLL - Kontrollaborleiter(in) qualification

Deine Vorteile