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Empleo > Prácticas > Logística/Supply Chain > Suiza > Detalles de la Oferta 

MSAT Intern 80-100

Lonza
Suiza  Suiza
Prácticas, Logística/Supply Chain, Inglés
11
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Descripción del puesto:

As an Intern (m/f/d) in the MSAT Growth Project at Lonza AG, you will gain hands-on experience in a highly regulated, science-driven biopharmaceutical environment. You will support the MSAT team in growth-focused initiatives related to drug product manufacturing, process optimization, and lifecycle management, contributing directly to technical projects that support business expansion and operational excellence. You will be part of an exciting Greenfield project in Stein AG Switzerland and will support the commercial readiness of a large-scale aseptic manufacturing facility for Biologics.

What you will get:
* Opportunity to work with a global team and contribute to high-impact projects.
* Mentorship and professional development opportunities.

What you will do:
In this role, you will work closely with MSAT experts and cross-functional stakeholders. Depending on project needs, your responsibilities may include:
* Support of MSAT tasks within a capital investment project to build and commission manufacturing units, ensuring commercial readiness for the GMP manufacturing facility.
* Support the qualification of manufacturing equipment and clean rooms
* Preparation of GMP documentation, technical reports, presentations, and project documentation for internal stakeholders
* Support in technology transfer, process improvements, or scale-up related activities
* Assistance in coordination of meetings, workshops, and project follow-ups
* Collaboration with cross-functional teams such as Manufacturing, QA, QC, Development, and Engineering
* Proactive contribution of ideas for process optimization, standardization, and efficiency improvements
* Compliance with Lonza quality systems, GMP requirements, and safety standards

What we are looking for:
* University Degree (Bachelor or Master) in a technical or scientific field such as Engineering, Biotechnology, Pharmacy, or a related field.
* Basic understanding of pharmaceutical drug product manufacturing process and GMP/cGMP principles
* Proficient in MS Office (Word, Excel, PowerPoint) and ability to work with technical documentation (SOPs, protocols, reports)
* Strong communication skills, able to translate complex technical topics into clear actionable messages
* Proactive, positive approach, problem-solving attitude, and ability to take full responsibility for assigned areas
* A very strong team player with a hands-on mentality
* Very good verbal and written communication skills as well as proficiency in English is a must; German language skills are a plus.

About Lonza
At Lonza, our people are our greatest strength. With 30+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now

Origen: Web de la compañía
Publicado: 11 Abr 2026  (comprobado el 15 Abr 2026)
Tipo de oferta: Prácticas
Idiomas: Inglés
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