KI-Beschreibung

In this role, you will focus on developing innovative parenteral packaging solutions for radioligand therapies. You will collaborate with diverse teams to create effective syringe systems while ensuring compliance and functionality throughout the process.

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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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  Demonstrated ability to lead and influence within a global, matrixed organization

Deine Vorteile

KI-Beschreibung

As a Senior Expert in Parenteral Packaging Technology, you will focus on developing innovative syringe systems for radioligand therapies, collaborating with diverse teams to ensure effective packaging solutions and compliance with regulatory standards.

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  Master’s or PhD in engineering, materials science, pharmaceutical technology, or related discipline
• •
  Minimum of 3 years’ experience in a comparable position, ideally within primary packaging, medical device, combination product development, or pharmaceutical industries
• •
  Demonstrated ability to lead and influence within a global, matrixed organization

Deine Vorteile

KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies and oversee submission activities, ensuring compliance and quality. This role involves proactive communication with stakeholders and leading interactions with Health Authorities to drive successful outcomes.

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  Minimum 5 years of regulatory CMC experience or pharmaceutical industry experience
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  Knowledge in regulatory submission and approval processes
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  Science degree or equivalent

Deine Vorteile

KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies and oversee submission activities, ensuring compliance and quality. This role involves proactive communication with teams and leading interactions with Health Authorities to support product development.

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  Minimum 5 years of regulatory CMC experience or pharmaceutical industry experience
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  Knowledge in regulatory submission and approval processes
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  Ability to critically evaluate data from various scientific disciplines

Deine Vorteile

KI-Beschreibung

In this role, you will lead E&L project activities, conduct studies using advanced analytical techniques, and collaborate with various stakeholders. Your expertise will help shape testing strategies and ensure compliance with evolving regulations.

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  University degree (preferably PhD) in Pharmacy, Polymer or Food Chemistry, Life Sciences or relevant science discipline
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  8+ years of working experience in pharma/
  biopharmaceutical industry or relevant industry
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  Expertise in analytical technologies: Headspace-GC/
  MS, LI-GC/
  (HR)MS, HPLC/
  (HR)MS, and related sample preparation techniques

Deine Vorteile

KI-Beschreibung

In this role, you will lead E&L project activities, conduct studies using advanced analytical techniques, and collaborate with various stakeholders. Your expertise will help adapt workflows and ensure compliance with evolving regulations in drug development.

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  University degree (preferably PhD) in Pharmacy, Polymer or Food Chemistry, Life Sciences or relevant science discipline
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  8+ years of working experience in pharma/
  biopharmaceutical industry or relevant industry
• •
  Expertise in analytical technologies: Headspace-GC/
  MS, LI-GC/
  (HR)MS, HPLC/
  (HR)MS, and related sample preparation techniques

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 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 lead data science and automation projects, driving innovation in biopharmaceutical development. Your work will involve collaboration with teams, enhancing digital initiatives, and conducting scientific experiments to support process characterization.

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

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

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 diverse team 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

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

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  MSc in Human Factors Engineering, Cognitive Sciences, Behavioral Sciences, Biomedical Engineering, Psychology, Product Design, or Mechanical Engineering
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  3+ years of experience in human factors engineering, preferably in medical devices or combination products
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  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. Your day-to-day responsibilities will include managing QA oversight for projects, fostering AI usage, and ensuring compliance with GMP standards while collaborating with various teams.

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  5+ years of relevant experience in development quality environment
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  Experience in project management or operations management
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  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 throughout project execution. Your day-to-day responsibilities will involve managing complex global projects, promoting AI usage, and collaborating closely with various teams to enhance operational efficiency.

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

Deine Vorteile

KI-Beschreibung

As an R&D Senior Quality Manager, you will play a crucial role in ensuring compliance with regulatory standards while supporting quality initiatives. Your day-to-day responsibilities will involve managing quality plans, addressing quality issues, and collaborating on projects to enhance operational excellence.

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  Quality assurance (QA)
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  Risk management
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  Agility

Deine Vorteile

KI-Beschreibung

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

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  Agility
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  Analytical development
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  Project management

Deine Vorteile

KI-Beschreibung

In this apprenticeship, you will immerse yourself in automation technology, working closely with experts to install systems, maintain machinery, and program controls. You will receive support from experienced trainers to shape your future.

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  Excellent compulsory school diploma or equivalent
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  Technical interest in mechanics and electronics
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  Careful and precise working style

KI-Beschreibung

In this apprenticeship, you will dive into the world of metalworking, mastering everything from high-precision mold manufacturing to operating CNC machines and maintaining essential tools.

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  Excellent compulsory school diploma or higher-level school diploma
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  Passion for craftsmanship
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  Strong interest in technology

KI-Beschreibung

In this role, you will be actively involved in the manufacturing process, executing tasks to ensure timely production while maintaining quality standards. You will also manage essential documentation and support operational activities, all while adhering to safety and GMP guidelines.

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  Operations management and execution
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  Transportation classification expertise (i.e. IATA or DOT)
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  Manufacturing process execution