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, generating experimental data, and evaluating new technologies to enhance processes.

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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 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 diverse 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 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 diverse 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 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 Substance Project Lead, you will coordinate a dedicated team and oversee all aspects of drug substance development, including process validation and budget management, while ensuring effective communication across various organizational levels.

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  Minimum of 5 years relevant experience in Biologics CMC development or production
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  MSc or PhD in Natural Science
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  Proficiency in English

Deine Vorteile

KI-Beschreibung

In this role, you will gain hands-on experience in analytical development, working on innovative projects while collaborating with a dedicated team. Daily tasks will involve method optimization, data analysis, and presenting findings, all aimed at improving patient care.

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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

KI-Beschreibung

In this role, you will immerse yourself in analytical development, working on innovative projects while collaborating with a dedicated team. Your responsibilities will include method optimization, data analysis, and presenting findings, all aimed at enhancing patient care.

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  Enrollment in a master's program in a relevant field
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  Interest or knowledge in data science, statistical data analysis, and process modeling, simulation, automation, and basic programming
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  Proficiency in MS Office for data analysis and documentation

Deine Vorteile

KI-Beschreibung

As a Drug Product Project Leader, you will drive the development of biologics, ensuring strategic alignment and timely delivery of high-quality documents while engaging with stakeholders and fostering team growth in a dynamic environment.

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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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  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 lead the scientific strategy for Biologic Drug Product development, overseeing all aspects from technical activities to regulatory submissions. Your expertise will drive innovation while mentoring junior team members and presenting findings to diverse audiences.

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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
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  Solid understanding of quality standards and regulations in pharmaceutical industry

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 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 while collaborating with project teams. Your expertise will guide interactions with health authorities and shape the regulatory landscape for innovative products.

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  Science degree or equivalent; advanced degree desired
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  At least 2 years’ experience in regulatory CMC or pharmaceutical industry
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  Working knowledge in regulatory submissions

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of developing innovative drug delivery devices, ensuring they are user-friendly and compliant with regulatory standards. Your work will involve conducting research, collaborating with various teams, and translating user needs into effective design solutions.

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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)
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  Experience with qualitative and quantitative research methods

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

Deine Vorteile

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 supporting quality initiatives. Your day-to-day responsibilities will include managing quality plans, addressing quality issues, and collaborating on projects to enhance operational excellence.

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  Agility
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  Analytical development
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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 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 be actively involved in the manufacturing process, executing tasks to ensure products are produced on time and meet quality standards. You will also manage important 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