KI-Beschreibung

In this apprenticeship, you will immerse yourself in automation technology, working closely with experts to install systems, maintain machinery, and engage in programming PLC controls and robots, all while building valuable teamwork skills.

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  Technical interest in mechanics and electronics
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  Careful and precise working style
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  Enthusiasm and commitment

KI-Beschreibung

In this apprenticeship, you will dive into the world of metalworking, mastering the creation of precision molds and the operation of advanced machinery while ensuring that tools are well-maintained and functional.

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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 role, you will drive the global regulatory strategy for CMC, ensuring compliance and quality in submissions. Your day-to-day responsibilities will involve collaborating with cross-functional teams, negotiating with health authorities, and providing strategic guidance to enhance project outcomes.

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

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

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. This role involves leading submission activities, managing risks, and collaborating with cross-functional teams to enhance patient outcomes.

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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 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 data 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 also collaborate with a dedicated team, documenting findings and presenting them to enhance drug substance processes.

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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, and basic programming
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  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
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  PhD or Master in relevant discipline
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  Solid understanding of quality standards

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

Deine Vorteile

KI-Beschreibung

In this role, you will drive global CMC regulatory strategies and oversee submission activities, ensuring compliance and quality throughout the product lifecycle. Your expertise will guide interactions with health authorities and support project teams in navigating regulatory challenges.

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  Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent
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  At least 2 years’ experience in regulatory CMC or pharmaceutical industry
• •
  Working knowledge in regulatory submissions

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 communication across teams to enhance quality processes.

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  5+ years of relevant experience
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  Demonstrated experience in project management
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  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.

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  5+ years of relevant experience
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  Demonstrated experience in project management
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  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
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  Critical negotiations
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  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

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. Your daily responsibilities will also include managing essential documentation to support 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