KI-Beschreibung

In this apprenticeship, you will dive into the world of metalworking, gaining hands-on experience in manufacturing injection molds and operating CNC machines while mastering essential machining techniques.

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  Excellent compulsory school diploma or higher-level school diploma
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  Passion for craftsmanship and strong interest in technology
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  Eagerness to learn and enjoyment of new challenges

KI-Beschreibung

In this apprenticeship, you will immerse yourself in automation technology, working closely with experts while gaining hands-on experience in the installation, maintenance, and programming of advanced systems.

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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 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 shaping global CMC regulatory strategies for innovative projects. Your day-to-day responsibilities will involve leading submission activities, ensuring compliance, and collaborating with cross-functional teams to drive successful interactions with Health Authorities.

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  Minimum 8 years regulatory experience or pharmaceutical industry experience
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  Substantial knowledge in regulatory submission and approval processes
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  Science degree (Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) 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 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 in regulatory submission and approval processes
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  Science degree or equivalent

Deine Vorteile

KI-Beschreibung

You will develop and implement global regulatory strategies for CMC, manage submission activities, and ensure compliance while collaborating with cross-functional teams and engaging with health authorities.

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  Minimum 8 years regulatory experience preferred
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  Substantial knowledge in regulatory submission
• •
  Proven ability to evaluate scientific data

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
• •
  Knowledge in regulatory submission and approval processes
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  Science degree or equivalent; advanced degree desired

Deine Vorteile

KI-Beschreibung

In this role, you will actively support the development of innovative drug candidates by conducting experiments and analyzing data. You will also document your findings and collaborate with the team to enhance processes, gaining valuable insights into drug substance development.

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  Enrollment in a Master’s program in life science
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  Interest or knowledge in data science, statistical analysis, process modeling, simulation, automation, and basic programming
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  Advanced communication skills in English

KI-Beschreibung

In this role, you will actively support the development of innovative drug candidates by conducting experiments and analyzing data. You will collaborate with a dedicated team, document findings, and present insights, gaining valuable experience in drug substance development.

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  Enrollment in a Master’s program in life science
• •
  Interest or knowledge in data science, statistical data analysis, process modeling, simulation, automation, and basic programming
• •
  Advanced communication skills in English

KI-Beschreibung

In this role, you will actively support the development of innovative drug candidates by conducting experiments and analyzing data. You will collaborate with a dedicated team, document findings, and present insights, gaining valuable experience in drug substance development.

• •
  Enrollment in a Master’s program in life science
• •
  Interest or knowledge in data science, statistical data analysis, process modeling, simulation, automation, and basic programming
• •
  Advanced communication skills in English

KI-Beschreibung

You lead scientific strategies and oversee technical activities in drug product development, ensuring timely delivery and compliance with quality standards while mentoring junior team members.

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  2-5 years in biotech/
  pharmaceutical industry
• •
  PhD or Master in relevant discipline
• •
  Solid understanding of quality standards

Deine Vorteile

KI-Beschreibung

You manage global CMC regulatory strategies and submissions, ensuring compliance and effective communication with stakeholders while leading interactions with health authorities.

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  At least 2 years’ regulatory CMC experience
• •
  Science degree or equivalent
• •
  Working knowledge of chemistry/
  biotechnology

Deine Vorteile

KI-Beschreibung

In this role, you will drive global CMC regulatory strategies and submissions, ensuring compliance while balancing innovation and business needs. Your day-to-day responsibilities will involve collaborating with project teams, managing documentation, and engaging with health authorities.

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  Science degree or equivalent
• •
  At least 2 years’ experience in regulatory CMC or pharmaceutical industry
• •
  Working knowledge of chemistry/
  biotechnology, analytics or pharmaceutical technology

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

You oversee quality assurance for Data and Digital projects, ensuring compliance and effective execution. Your role involves leading initiatives, promoting the use of AI, and maintaining communication across teams to enhance quality processes.

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  5+ years of relevant experience
• •
  Demonstrated experience in project management
• •
  Strong quality background

Deine Vorteile

KI-Beschreibung

You oversee quality assurance for Data and Digital projects, ensuring compliance and effective execution. Your role involves leading initiatives, promoting the use of AI, and maintaining regulatory standards while collaborating with various teams.

• •
  5+ years of relevant experience
• •
  Demonstrated experience in project management
• •
  Strong quality background

Deine Vorteile

KI-Beschreibung

You manage quality assurance and compliance initiatives, ensuring adherence to regulations and fostering continuous improvement in clinical programs while addressing quality issues and supporting corrective actions.

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  Functional breadth
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  Critical negotiations
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  Project management

Deine Vorteile

KI-Beschreibung

You manage quality assurance tasks, ensuring compliance with regulations and supporting initiatives to improve quality performance across clinical programs and operational activities.

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  Functional breadth
• •
  Critical negotiations
• •
  Project 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.

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

Deine Vorteile