KI-Beschreibung

As a Senior Manager in RA CMC, you will shape global regulatory strategies and oversee submission activities, ensuring compliance while driving innovation. This role involves collaborating with teams, managing risks, and engaging 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 of 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 for drug development, ensuring compliance while driving innovation. Your role involves leading submission activities, managing documentation, and engaging with Health Authorities to navigate the regulatory landscape.

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

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
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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.

• •
  University degree (preferably PhD) in Pharmacy, Polymer or Food Chemistry, Life Sciences or relevant science discipline
• •
  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 design scalable software solutions for manufacturing while collaborating with cross-functional teams. Your work will focus on enhancing data analytics capabilities and driving continuous improvement across systems.

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  Bachelor’s or Master’s degree in Computer Science, Data Science, Software Engineering, Automation Engineering, or related field with strong IT/
  Data focus
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  Minimum 4 years of relevant professional experience
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  Solid foundation in data engineering

Deine Vorteile

KI-Beschreibung

In this role, you will design scalable software solutions for manufacturing while collaborating with cross-functional teams. Your work will focus on enhancing cloud-based analytics and ensuring alignment with business strategies.

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  Bachelor’s or Master’s degree in Computer Science, Data Science, Software Engineering, Automation Engineering, or related field
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  Minimum 4 years of relevant professional experience
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  Solid foundation in data engineering

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 include leading key projects, coaching experts, and overseeing major transformations in DSP development.

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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 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 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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  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
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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 with project managers and scientists. Your daily responsibilities will include designing technical activities, managing technology transfers, and presenting findings to diverse audiences.

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  Experience of 2-5 years 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 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 data science and automation projects, driving innovation in biopharmaceutical development. Your expertise will help shape strategies, enhance digital initiatives, and ensure alignment with business goals while working on cutting-edge technologies.

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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 data science and automation projects, driving innovation in biopharmaceutical development. Your work will involve collaborating with teams, enhancing automation strategies, and ensuring alignment with business goals.

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  Completed studies in Biotechnology, Process Engineering, Biology, Pharmaceutical Technology, Technical Chemistry, Pharmacy, Data Science, or Computer Science (or comparable)
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  Experience in data science, data engineering, and automation
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  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 and support regulatory submissions while collaborating with internal 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, 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 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

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 generating and analyzing critical data for medical devices, ensuring compliance with regulations, and leading innovative lab projects. Your day-to-day responsibilities will involve testing, documentation, and collaboration with project teams to enhance product quality.

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  Apprenticeship or secondary school, or bachelor's or master's degree in Technical/
  Engineering/
  Life-Sciences
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  Experience 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

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.

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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, promoting 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 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 activities.

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

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

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 adhering to quality and safety standards. You will also manage important documentation to support efficient operations.

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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