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.

• •
  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
• •
  Hands-on experience in wet-lab bioprocess development and in-silico modeling approaches
• •
  Proficiency in mechanistic modeling, machine learning, digital twin development, chemometrics, multivariate analysis, and regression

Deine Vorteile

KI-Beschreibung

In this role, you will lead the development of upstream cell culture processes, utilizing expertise in bioprocess modeling and AI to enhance production efficiency. The work involves designing experiments, collaborating globally, and mentoring junior scientists, all while contributing to innovative biotherapeutic solutions.

• •
  PhD in Biotechnology, (Bio)chemical Engineering, or related field
• •
  2+ years of experience in bioprocess development, modeling, and digitalization
• •
  Hands-on experience in wet-lab bioprocess development and in-silico modeling

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 standards, and driving innovation in lab automation.

• •
  Automation experience
• •
  Minimum 5 years of experience
• •
  Coding in Python and C#

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 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 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.

• •
  Ph.D. in biotechnology, biochemical engineering, biochemistry, molecular biology, biology, chemistry, chemical engineering, or related field
• •
  Proven track record in downstream process development
• •
  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.

• •
  PhD in Biotechnology, Biochemical or Bioprocess Engineering, or related field
• •
  6+ years of experience in USP process development or 8+ years of relevant experience with MSc
• •
  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.

• •
  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 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 exchange.

• •
  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 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.

• •
  University degree in life sciences, biotechnology, bioprocess engineering, or equivalent
• •
  PhD with minimum 2 years or Master with minimum 6 years industrial experience or equivalent
• •
  Proven experience in upstream process transfer and collaboration with CMOs

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.

• •
  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 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.

• •
  University degree in life sciences, biotechnology, bioprocess engineering, or equivalent
• •
  PhD with minimum 2 years or Master with minimum 6 years industrial experience or equivalent
• •
  Proven experience in upstream process transfer and collaboration with CMOs

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 driving innovation in drug development.

• •
  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 data science and automation projects, driving innovation in biopharmaceutical development. Your expertise will shape strategies, enhance digital initiatives, and ensure alignment with business goals.

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

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.

• •
  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 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, and preparing scientific documents for regulatory submissions.

• •
  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 tackle complex biopharmaceutical challenges by developing robust models that inform 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.

• •
  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

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.

• •
  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 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.

• •
  Microbiology or finalized apprenticeship in Pharmaceutical industry or equivalent
• •
  Fluency in German and intermediate proficiency in English
• •
  GMP procedures

Deine Vorteile

KI-Beschreibung

In this part-time role, you will play a crucial part in maintaining product quality and ensuring compliance with GxP standards. Daily tasks will involve overseeing quality systems, managing deviations, and supporting product release and validation projects.

• •
  Microbiology or finalized apprenticeship in the Pharmaceutical industry, or equivalent
• •
  Fluency in German and intermediate proficiency in English

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, 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 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 QA Operations Team Leader, you will guide a team of Qualified Persons to ensure the compliant release of pharmaceutical products. This role involves managing resources, resolving quality issues, and fostering a culture of continuous improvement.

• •
  Minimum 7 years of experience in Quality Assurance within the pharmaceutical industry
• •
  Qualified Person (QP) as per EU Directive 2001/
  83/
  EC
• •
  Extensive knowledge of EU GMP regulations and relevant national legislation

Deine Vorteile

KI-Beschreibung

As a QA Operations Team Leader, you will guide a team of Qualified Persons to ensure the compliant release of pharmaceutical products. This role involves managing resources, resolving quality issues, and fostering a culture of continuous improvement.

• •
  Minimum 7 years of experience in Quality Assurance
• •
  Qualified Person (QP) as per EU Directive 2001/
  83/
  EC
• •
  Minimum 4 years of experience as a certified Qualified Person (QP)

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing user-friendly drug delivery devices. Your daily work will involve conducting research, collaborating with diverse teams, and ensuring that products meet regulatory standards while prioritizing the end-user experience.

• •
  MSc in Human Factors Engineering, Cognitive Sciences, Behavioral Sciences, Biomedical Engineering, Psychology, Product Design, or Mechanical Engineering
• •
  3+ years of experience in human factors engineering, preferably in medical devices or combination products
• •
  Strong understanding of usability engineering standards (e.g., IEC 62366, ISO 14971)

KI-Beschreibung

In this role, you will oversee the integration of new technologies in TRD and drive digitalization strategies, ensuring quality assurance throughout project execution. Your day-to-day responsibilities will involve managing complex global projects, fostering AI usage, and maintaining compliance with GMP standards.

• •
  5+ years of relevant experience in development quality environment
• •
  Experience in project management or operations management
• •
  Strong quality background

Deine Vorteile

KI-Beschreibung

In this role, you will oversee the integration of new technologies in TRD and drive digitalization strategies, ensuring quality assurance across various projects. Your day-to-day responsibilities will involve collaborating with teams, managing complex projects, and promoting AI usage to enhance operational efficiency.

• •
  5+ years of relevant experience in development quality environment
• •
  Experience in project management or operations management
• •
  Strong quality background and innovation in Data & Digital

Deine Vorteile

KI-Beschreibung

As an R&D Senior Quality Manager, you will play a crucial role in ensuring compliance with regulatory standards while managing quality initiatives. Your day-to-day responsibilities will involve supporting inspections, developing quality plans, and driving improvements in operational quality and compliance.

• •
  Project management skills
• •
  Critical negotiation skills
• •
  Agility, analytical development

Deine Vorteile

KI-Beschreibung

As an R&D Senior Quality Manager, you will play a crucial role in ensuring compliance with regulatory standards while managing quality initiatives. Your daily responsibilities will include supporting inspections, enhancing operational quality, and addressing compliance issues.

• •
  Agility
• •
  Analytical development
• •
  Quality management

Deine Vorteile

KI-Beschreibung

In this role, you will lead the Site ITOT organization, focusing on enhancing automation and IT processes. Your daily responsibilities will include managing a dedicated team, collaborating with global counterparts, and ensuring operational excellence and compliance.

• •
  Minimum of 7 years of experience in Automation or IT in a GMP Pharma environment
• •
  In-depth knowledge of automation systems and IT infrastructure
• •
  Bachelor's degree in Computer Science, Information Technology, automation, engineering, or related field

Deine Vorteile

KI-Beschreibung

In dieser Rolle übernimmst du die Organisation der Abteilungen Baumschule und Saisonpflanzen und führst ein Team von rund 6 Mitarbeiter:innen. Du sorgst für eine ansprechende Warenpräsentation und unterstützt aktiv bei der Kundenberatung.

• •
  Einschlägige Ausbildung oder Berufserfahrung
• •
  Fachwissen im Pflanzenbereich
• •
  Sicherer Umgang mit EDV-Anwendungen

Deine Vorteile