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

Deine Vorteile

KI-Beschreibung

As a Process Expert, you will play a crucial role in biopharmaceutical production by providing expert support, ensuring compliance with GMP standards, and driving continuous improvement initiatives. Your daily responsibilities will involve collaborating with various stakeholders and training production personnel to maintain high-quality operations.

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  Completed studies in Biotechnology, Molecular Biology, Microbiology, Chemistry, or similar
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  Bachelor's degree with three years of professional experience, Master's degree with one year of professional experience, or PhD
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  Work experience in the pharmaceutical industry

Deine Vorteile

KI-Beschreibung

As a Process Expert, you will play a crucial role in biopharmaceutical production by providing expert support, ensuring compliance with GMP standards, and driving continuous improvement initiatives. Your daily responsibilities will include collaborating with various stakeholders, preparing essential documents, and training production staff.

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  Completed studies in Biotechnology, Molecular Biology, Microbiology, Chemistry, or comparable studies
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  Bachelor's degree with three years of professional experience
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  Proficiency in German and English (spoken & written)

Deine Vorteile

KI-Beschreibung

In this role, you will lead upstream cell culture process development, utilizing expertise in bioprocess modeling and AI to transform data into actionable insights. The position involves collaboration across teams, mentoring junior associates, and contributing to innovative scientific advancements.

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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

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 shaping key financial processes and project proposals.

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  Solid understanding of financial accounting principles
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  Experience supporting financial activities
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  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
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  Ability to perform accurate data analysis
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  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
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  Significant working experience in pharmaceutical industry in combination product development
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  Proven knowledge in late phase parenteral analytical development

Deine Vorteile

KI-Beschreibung

In this role, you will actively drive lab automation and digitalization efforts, implement new technologies, and conduct cell culture experiments. Your daily responsibilities will include troubleshooting, mentoring junior 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 6 years of experience in a related field
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  Strong practical experience in a laboratory and/
  or pilot plant environment

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 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.

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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
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  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 analytical data packages for drug-device combination products, coordinating project tasks, and leading cross-functional strategies. Your expertise will guide regulatory submissions and ensure successful product registrations.

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  Master or PhD in engineering, chemical/
  bio analytics, or equivalent
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  Significant working experience in pharmaceutical industry in combination product development
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  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 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
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  Strong understanding of regulatory requirements

Deine Vorteile

KI-Beschreibung

In this role, you will drive innovation and strategy in upstream process development, collaborating with global teams and leading initiatives that enhance scientific capabilities and ensure compliance in 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 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 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
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  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
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  PhD or Master in pharmaceutical technology, biotechnology, chemical engineering, or relevant discipline
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  Solid understanding of quality standards and regulations in pharmaceutical industry

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development and transfer of upstream cell culture processes, collaborating with cross-functional teams to ensure robust production methods. Your expertise will help integrate innovative processes and mentor junior associates, while contributing to life-changing medicines for patients worldwide.

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  University degree in life sciences, biotechnology, bioprocess engineering, or equivalent
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  Proven experience in upstream process transfer and collaboration with CMOs
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  Experience with statistical methods (DoE, MVDA) and data-driven or mechanistic models

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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  2-5 years of experience in biotech/
  pharmaceutical industry with focus on formulation or manufacturing processes development, technical transfer, validation, and submission
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  PhD or Master in pharmaceutical technology, biotechnology, chemical engineering, or relevant discipline
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  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 driving innovative solutions.

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  PhD or Master in pharmaceutical technology, biotechnology, chemical engineering, or relevant discipline
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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
• •
  Solid understanding of quality standards and regulations in pharmaceutical industry

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 engaged team culture.

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  Master or PhD in engineering, pharmaceutical field, or equivalent
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  Extensive working experience in pharmaceutical industry
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  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 quality and efficiency. You will also train staff and collaborate on continuous improvements to deliver vital medications globally.

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

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.

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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 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 environment.

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

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
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  Proficiency in English

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 gewährleisten.

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  Verhandlungssichere Deutsch- und Englischkenntnisse
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  Abgeschlossene wissenschaftliche oder technische Ausbildung
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  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.

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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 global team of experts 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, QbD, GMP, and regulatory requirements

Deine Vorteile

KI-Beschreibung

In dieser befristeten Position als Automatisierungstechniker:in bist du für die Wartung und Optimierung von Inspektions- und Verpackungslinien im Pharmaumfeld verantwortlich. Dein Alltag umfasst technische Klärungen, Schulungen und die Dokumentation deiner Tätigkeiten im SAP-System.

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  2-3 Jahre technische Erfahrung mit Automatisierungssystemen
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  Erfahrung mit MS Office und SAP
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  Abgeschlossene Lehre in technischem Bereich

Deine Vorteile

KI-Beschreibung

In dieser befristeten Position als Automatisierungstechniker:in bist du für die Wartung und Optimierung von Inspektions- und Verpackungslinien verantwortlich. Dein Alltag umfasst technische Klärungen, Schulungen von Mitarbeitenden und die Dokumentation deiner Tätigkeiten im SAP-System.

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  2-3 Jahre technische Erfahrung mit Automatisierungssystemen
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  Abgeschlossene Lehre in einem technischen Bereich
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  Erfahrung mit MS Office & SAP

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of generating and analyzing critical data for medical devices, ensuring compliance with regulations, and leading innovative projects. Your day-to-day responsibilities will involve collaborating with teams, conducting tests, and enhancing lab processes.

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  Apprenticeship or secondary school, or bachelor's or master's degree in Technical/
  Engineering/
  Life-Sciences area with substantial relevant work experience
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  Knowledge in Environment, Experiments Design, Health And Safety (EHS), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, SOP (Standard Operating Procedure), Technical Writing, Waterfall Model

Deine Vorteile

KI-Beschreibung

As a Technical Transfer Lead, you will play a crucial role in managing project teams and coordinating with various functions to ensure the successful transfer of innovative pharmaceuticals. Your day-to-day responsibilities will include overseeing technology transfers, supporting registration activities, and optimizing processes to enhance product delivery.

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  Minimum 3 years of relevant experience in pharmaceutical manufacturing
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  University degree (MSc. or PhD) in Biology, Biochemistry, Biotechnology, Biochemical Engineering, or equivalent experience
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  Solid experience in Project Management

Deine Vorteile