KI-Beschreibung

In this role, you will leverage your organizational skills to ensure smooth daily operations by coordinating meetings and events while optimizing workflows. Your proactive approach will foster collaboration and support the onboarding of new team members.

• •
  Proficiency in Microsoft Office Suite
• •
  Proven experience in administrative roles
• •
  Excellent verbal and written communication skills in German and English

Deine Vorteile

KI-Beschreibung

In this role, you will leverage your organizational skills to ensure smooth daily operations, coordinate impactful meetings and events, and enhance administrative processes while fostering collaboration across teams.

• •
  Proficiency in Microsoft Office Suite
• •
  Excellent verbal and written communication skills in German and English
• •
  Proven experience in administrative roles

Deine Vorteile

KI-Beschreibung

In dieser Rolle als Mechatroniker:in für Abfüllung und visuelle Inspektion bist du verantwortlich für die Wartung und Instandhaltung modernster Anlagentechnologie, um die sichere Bereitstellung hochwertiger Arzneimittel zu gewährleisten. Dein Alltag umfasst die Überwachung von Produktionsabläufen und die technische Betreuung von Pharma-Anlagen, während du kontinuierliche Verbesserungen vorantreibst.

• •
  Abgeschlossene Lehre in einem einschlägigen Fachbereich
• •
  Technisches Verständnis von korrektiver und präventiver Wartung
• •
  Gute Deutschkenntnisse

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

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.

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  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 dieser Rolle als Mechatroniker:in für Abfüllung und visuelle Inspektion bist du verantwortlich für die Wartung und Instandhaltung modernster Anlagentechnologie, um die sichere Bereitstellung hochwertiger Arzneimittel zu gewährleisten.

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

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of lab automation and digitalization, implementing new technologies and driving initiatives that enhance efficiency. A hands-on approach will involve planning experiments, mentoring team members, and ensuring compliance with quality standards.

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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 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.

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  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 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

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
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  MSc or PhD in Natural Science
• •
  Proficiency in English

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
• •
  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 technische Teams bei Fehleranalysen, um die Anlagenverfügbarkeit zu gewährleisten.

• •
  Abgeschlossene Lehre als Metalltechniker, Mechaniker, Mechatroniker oder vergleichbar
• •
  Sehr gute Deutschkenntnisse und Englischkenntnisse von Vorteil
• •
  Genaues Arbeiten, Teamfähigkeit, Interesse am Bereitschaftsdienst

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
• •
  Mehrjährige Erfahrung in pharmazeutischer Produktion, Technologie-Transfer oder MS&T
• •
  Fundierte Kenntnisse in cGMP, Validierung und regulatorischen Anforderungen

Deine Vorteile

KI-Beschreibung

In this role, you will transform financial data into actionable insights, supporting managers and senior colleagues with analysis that drives reporting and project decisions. Your attention to detail will ensure accuracy and compliance in all financial processes.

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  Solid understanding of financial accounting principles
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  Ability to perform accurate data analysis
• •
  Experience using MS Excel

Deine Vorteile

KI-Beschreibung

In this role, you will transform financial data into actionable insights, ensuring accuracy and compliance while supporting managers with analysis and reporting. Your contributions will be vital in maintaining financial integrity and driving informed decision-making.

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  Solid understanding of financial accounting principles
• •
  Ability to perform accurate data analysis
• •
  Experience using MS Excel

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 others, 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 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 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.

• •
  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 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 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.

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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 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
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  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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  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 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.

• •
  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 leverage MES expertise to enhance pharmaceutical manufacturing processes, ensuring quality and efficiency. Daily activities will involve troubleshooting, collaborating on improvements, and training staff to optimize the use of MES PAS-X.

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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 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.

• •
  Master or PhD in engineering, pharmaceutical field, or equivalent
• •
  Extensive working experience in pharmaceutical industry
• •
  Excellent skills in leading people and projects

Deine Vorteile

KI-Beschreibung

In this role, you will leverage your MES expertise to enhance pharmaceutical manufacturing processes, ensuring efficient operations and quality control while training staff and driving continuous improvement initiatives.

• •
  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 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.

• •
  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 dieser Rolle bist du die zentrale Schnittstelle zwischen Novartis und den Behörden. Du koordinierst Verhandlungen, sorgst für die Einhaltung von Vorschriften und unterstützt das Kontraktorenmanagement, um einen sicheren und umweltfreundlichen Arbeitsplatz zu fördern.

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  Verhandlungssichere Deutschkenntnisse
• •
  Abgeschlossene wissenschaftliche oder technische Ausbildung
• •
  Kenntnisse der österreichischen Rechtsgebung

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