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, 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
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  Strong interest in technology

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 overseeing major transformations while collaborating across teams.

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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 coordinate analytical tasks for drug-device combination products, manage project resources, and lead partnerships with testing laboratories. Your expertise will shape regulatory documents and analytical strategies, ensuring successful product registrations and inspections.

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  Master or PhD in engineering, chemical/
  bio analytics, or equivalent
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  Significant working experience in pharmaceutical industry in combination product development
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  Proven knowledge in late phase parenteral analytical development

Deine Vorteile

KI-Beschreibung

In this role, you will lead a team focused on identifying and mitigating risks in drug-device combination products. You will ensure that quality control strategies align with regulatory standards while fostering a high-performing and engaged team culture.

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  Master or PhD in engineering, pharmaceutical field, or equivalent
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  Extensive working experience in pharmaceutical industry
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  Excellent skills in leading people and projects

Deine Vorteile

KI-Beschreibung

In this role, you will lead a team focused on identifying and mitigating risks in drug-device combination products. You will ensure that quality control strategies align with regulatory standards while fostering a high-performing and engaged team culture.

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  Master or PhD in engineering, pharmaceutical field, or equivalent
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  Extensive working experience in pharmaceutical industry
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  Proven knowledge in risk management and control strategy

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.

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  Experience in data science, data engineering, and automation
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  Proficiency in programming languages such as Python, R, or SQL
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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 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, ideally with several years of industry experience
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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

In this role, you will engage in innovative analytical development projects, learning to optimize methods while collaborating with a dedicated team. Your contributions will directly impact the development of biopharmaceutical products for patients worldwide.

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  Enrollment in a master's program in a relevant field
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  Interest or knowledge in data science and statistical analysis
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  Proficiency in MS Office for data analysis

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.

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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 projects. Your day-to-day responsibilities will involve collaborating with teams, conducting tests, and enhancing lab processes.

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  Apprenticeship or secondary school, or bachelor's or master's degree in Technical/
  Engineering/
  Life-Sciences area with substantial relevant work experience
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  Knowledge 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 quality assurance, manage complex global projects, and ensure compliance with GMP standards. Your work will involve collaborating with various teams to drive digitalization and enhance quality processes within TRD.

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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 include managing quality plans, conducting audits, and collaborating on process improvements to enhance operational quality.

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  Agility
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  Analytical development
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  Quality management

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.

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  Project management skills
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  Critical negotiation skills
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  Agility, analytical development

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