KI-Beschreibung

In this role, you will lead impactful projects and drive technology changes within Lonza's Integrated Biologics network. Your expertise will help resolve complex challenges, mentor scientists, and contribute to growth and innovation in bioprocessing.

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  10+ years of experience in upstream development in GMP environment
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  Advanced degree in chemical engineering, biotechnology, or related field
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  Strong leadership and project management skills

Deine Vorteile

KI-Beschreibung

In this internship, you will engage in hands-on laboratory work, focusing on transferring innovative upstream processes to pilot scales. Daily tasks will involve designing experiments, analyzing data, and collaborating with experienced scientists.

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  Bachelor's degree in biotechnology
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  English speaking and writing skills

KI-Beschreibung

In this role, you will lead a dynamic team focused on process validation for mammalian manufacturing. Your day-to-day responsibilities will include overseeing validation activities, collaborating with cross-functional teams, and ensuring compliance with regulatory standards.

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  Minimum 5 years of experience in process validation within a cGMP-regulated biopharmaceutical environment
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  Proven leadership experience in managing technical teams and complex projects
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  Bachelor’s, Master’s, or PhD degree in biotechnology, chemical engineering, or related disciplines

KI-Beschreibung

In this role, you will be at the forefront of drug product manufacturing, ensuring compliance with cGMP standards while troubleshooting production issues and providing training and technical guidance to the team.

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  2-4 years of experience in GMP environment on the shopfloor or completed EFZ apprenticeship as a mechanic or related profession
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  Familiarity with GMP requirements, quality procedures, and SOP execution
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  IT knowledge and knowledge in SAP and MES

Deine Vorteile

KI-Beschreibung

In this role, you will engage in process validation for mammalian manufacturing, ensuring compliance with regulatory standards while collaborating with various teams. Your expertise will be vital in managing technical risks and representing the organization in key meetings.

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  Minimum 1 year of experience in process validation within a cGMP-regulated biopharmaceutical environment
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  Proven experience in managing complex projects
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  Bachelor’s, Master’s or PhD degree in biotechnology, chemical engineering or related disciplines

KI-Beschreibung

In this role, you will focus on assessing workplace health hazards and conducting exposure monitoring. You will also deliver training to promote safe practices, maintain crucial databases, and collaborate with teams to ensure compliance and improve health protection.

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  Minimum 5 years of experience in analytical chemistry or biology, and in chemical or biological production
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  Strong process understanding in Biopharma manufacturing, with emphasis on cGMP, safety, and biosafety compliance
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  MS in Natural Science, Analytical Chemistry, Chemistry, or Biology

Deine Vorteile

KI-Beschreibung

As an EHS Design and Compliance Engineer specializing in Fire Safety, you will play a crucial role in ensuring that fire protection standards are met throughout investment projects, from feasibility to design, while fostering a strong EHS culture.

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  Experience in pharmaceutical engineering construction, ideally in bio-pharmaceutical industry or manufacturing
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  5-10 years in EHS design and compliance
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  Proven process understanding of design safety and legal safety demands in pharmaceutical environment or similar

KI-Beschreibung

In this QA internship, you will actively support quality assurance activities, ensuring compliance with industry standards while collaborating with various teams to foster continuous improvement in production and documentation processes.

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  Enrollment in or completion of Bachelors or Masters in Pharmacy, Pharmaceutical Sciences, Biotechnology, Biochemistry, Biology, or related field
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  Fluency in written and spoken English
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  Prior experience in a research laboratory environment

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of production expertise, ensuring the successful setup and qualification of manufacturing units while maintaining high safety and quality standards in clinical and commercial BioConjugates projects.

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  Master's Degree in Biotechnology, Biochemical Engineering, Biochemistry, or related Life Science subject
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  Over 4 years of professional experience in downstream processing (DSP) within biotechnology production
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  Strong knowledge of Bioconjugates and Automation (MES/
  DeltaV)

Deine Vorteile

KI-Beschreibung

In this role, you will be at the forefront of production expertise, ensuring the successful setup and qualification of manufacturing units while maintaining high safety and quality standards in the production of therapeutic BioConjugates.

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  Master's Degree in Biotechnology, Biochemical Engineering, Biochemistry, or related Life Science subject
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  Over 4 years of professional experience in downstream processing (DSP) within biotechnology production
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  Strong knowledge of Bioconjugates and Automation (MES/
  DeltaV)

Deine Vorteile

KI-Beschreibung

As a QA Manufacturing Specialist, you will ensure product quality by overseeing manufacturing processes, monitoring compliance with GMP standards, and providing hands-on training to operators. This role is vital in maintaining rigorous quality practices on the shop floor.

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  Strong background in quality assurance within pharmaceutical or regulated manufacturing environment
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  Good understanding of aseptic process and core requirements
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  Excellent communication and coaching skills

Deine Vorteile

KI-Beschreibung

As a QA Manufacturing Lead, you will ensure product quality by overseeing manufacturing processes, monitoring compliance with GMP standards, and providing hands-on training to the team. This role involves real-time support, documentation review, and active participation in audits, making a significant impact on the quality culture.

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  Strong background in quality assurance in pharmaceutical or regulated manufacturing
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  Solid understanding of GMP (Good Manufacturing Practices)
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  Excellent communication and coaching skills

Deine Vorteile

KI-Beschreibung

In this role, you will lead quality assurance efforts in a sterile manufacturing environment, ensuring compliance and operational excellence while overseeing major projects and facility expansions. Your expertise will be crucial in guiding teams through new technologies and maintaining high-quality standards.

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  Deep expertise in aseptic operations
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  Proven QA leadership experience
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  Experience supporting major capital projects

Deine Vorteile

KI-Beschreibung

In this role, you will automate workflows and transform raw data into actionable insights. Your day-to-day responsibilities will include writing SQL queries, building ETL pipelines, and collaborating with various teams to enhance data integrity and accessibility.

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  Good SQL expertise
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  Experience with enterprise data platforms
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  Proven skills in ETL, automation, and BI dashboard development

Deine Vorteile

KI-Beschreibung

You manage supply chain systems by overseeing project execution, ensuring effective communication with stakeholders, and driving continuous improvement in processes and data management while maintaining regulatory compliance.

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  8+ years of experience in commercial pharmaceutical/
  biotech
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  Completed multiple SAP S/
  4 HANA implementations
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  PMP or similar project management certification

Deine Vorteile

KI-Beschreibung

In this role, you will ensure that Environmental, Health, and Safety requirements are met throughout investment projects, from feasibility studies to detailed design. You will foster a strong EHS culture and conduct essential safety assessments.

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  EHS specialization in Process Safety or Fire Safety

KI-Beschreibung

You will lead the development of materials and chemical processes while managing laboratory work and data analysis. Building customer relationships and mentoring lab technicians are also essential aspects of this role.

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  Advanced degree in material science
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  Significant knowledge of material characterization
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  Enjoy experimental work in the laboratory

KI-Beschreibung

You manage quality control processes, ensuring compliance with regulations and standards while overseeing testing, documentation, and method validation in partnership with contract laboratories.

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  Bachelor of Science
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  Minimum 9 years of experience
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  Excellent experience in managing CDMOs

Deine Vorteile

KI-Beschreibung

As a Trainee ERP Specialist, you will optimize ERP systems by managing part codes, developing BOMs, and ensuring compliance with SOPs. This role involves collaborating with teams to enhance processes and train others, making a significant impact on operational efficiency.

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  Degree or equivalent experience in Supply Chain Management or Business Management
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  Advanced experience in Supply Chain and Operations
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  Expertise in SAP Skills modules MM and PP